Lediga jobb QRIOS Minds AB i Göteborg

På uppdrag av vår världsledande samarbetspartner söker vi nu en driven laboratorieingenjör med intresse att utveckla nya hälsofrämjande produkter. Konsultuppdraget kommer att starta omgående och vara baserad i Göteborg.
Uppdragslängden är 6 månader.

Om tjänsten
I rollen som laboratorieingenjör kommer du snabbt fördjupa dina labbfärdigheter och bredda ditt professionella nätverk. Du kommer att ingå i ett framgångsrikt labbteam vars gemensamma målsättning är att utveckla nya hälsofrämjande produkter med fokus på cirkulär hållbarhet.

Dina arbetsuppgifter i huvudsak
Dina arbetsuppgifter innefattar bland annat att:
• Planera, testa, analysera och statistiskt utvärdera olika material som utvecklas inom bolaget.
• Presentera, dokumentera och rapportera testresultat
• Upprätthålla kunskap om testmetoder för att stötta kollegor på andra avdelningar i bolaget med specifika materialanalyser
• Delta i innovationsprojekt samt arbeta i tvärfunktionella team
• Utveckla, utvärdera och validera nya laboratoriemetoder för att möta konsumenternas och företagens behov

Vem är du?
För att ha rätt förutsättningar i rollen ser vi att du har:
• Teknisk universitetsexamen (minst kandidatexamen helst i kemi, mekanisk/material eller textil)
• God erfarenhet av statistisk analys och analytisk förmåga är meriterande
• God kommunikations- och presentationsförmåga i såväl skriftliga rapporter som i diskussioner
• Behärskar svenska och engelska i tal och skrift

Det är mycket meriterande om du har tidigare erfarenhet av labbarbete i industrin!


Om verksamheten
Detta är ett konsultuppdrag hos kund i 6 månader till att börja med. Under tiden är du anställd hos oss på QRIOS.
QRIOS kan erbjuda flera möjligheter till dig som är ingenjör eller har en teknisk bakgrund. Våra uppdragsgivare finns inom olika branscher där du får möjlighet att påverka och utvecklas i din roll.


Varmt välkommen med din ansökan. Urval sker löpande, ansök därför redan idag genom att klicka på ansök på https://www.qrios.se. Visa mindre

Are you interested in a challenging opportunity within the Development Quality function in one of the world’s leading pharmaceutical companies?

The Development Quality function is responsible for quality oversight of the pharmaceutical development activities in AstraZeneca. We are now looking for a Quality Advisor with GMP focus and an eye for details to our Gothenburg team. AstraZeneca’s pharmaceutical development organizations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase.

About the position
Responsible for quality release of manufactured Drug Product, Investigational Medicinal Product for clinical trials
Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects related to drug product
Providing quality advice and approval of documentation related to equipments, facilities, IT systems and instruments e.g. maintenance, calibration, validation and change control
Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards
Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working

Responsibilities
As a Quality Advisor, you will work with early product development manufacturing and packaging teams and be responsible for Development Quality release of externally manufactured Drug Product and Investigational Medicinal Product for clinical trials. You are expected to assure that activities and processes across the development chain are delivered to appropriate standards to meet regulatory expectations and assure product integrity and acceptability.

You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting. In your role you will have interactions with internal and external stakeholders.

Typical Accountabilities:
• Responsible for quality Release of manufactured Drug Product, Investigational Medicinal Product for clinical trials.
• Providing quality input to Manufacturing, Packaging, Labelling & Distribution activities.
• Providing proactive quality advice to support the development, implementation, and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards.
• Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects.
• Provide appropriate Quality Assurance input to business improvement projects.
• Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working.

Your profile
Requirements:
• Degree in pharmacy or engineering (specializing in Pharmaceuticals)
• 2-3 years’ experience of working within a pharmaceutical GMP environment.
• Understanding of Quality Systems and GMP and related activities to Investigational Medicinal Product (IMP).
• Experience of documentation, deviations, changes, and other quality and compliance
decisions in the development projects.
• Experience preferably within a pharmaceutical manufacturing organization is desirable
• Understanding of Project Management processes is desirable
• Fluent in written and spoken English.

Softskills/personal skills:

• Good team working and networking skills.
• Capable of making effective decisions.
• Demonstrate drive and energy in the role to make a difference.
• Demonstrate a high degree of personal credibility.
• Comprehensive understanding of the pharmaceutical/drug development process.
• Good communicator with experience of interacting effectively across interfaces.

About the organisation
This is a consultant assignement for 12 months at AstraZeneca Göteborg. During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives – and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

Biobank scientists are responsible for the storage and timely supply of human biological samples (HBS) to AZ research projects. HBS are received from e.g. clinical studies or academic collaborations, stored in local biobanks and distributed to projects. The group primarily supports the Sweden Region but partners with other Biobank groups within the Biosamples department globally to provide efficient support across AZ and our partner organisations.

The Biobank group works collaboratively to provide support within agreed service levels with a strong focus on our customers. We strive hard to understand what fits their needs best and to add value through our services. With an increased focus on the value and use of biobank samples we actively seek ways to improve our process or exploit new technology to build a cutting edge facility.


About the position
We are currently recruiting for a temporary Biobank Scientist in the AZ Gothenburg Biobank group within the global Precision Medicine and Biosamples organization. This position will provide the opportunity to work in a dynamic and enthusiastic environment whilst supplying a critical service to drug discovery projects. The work is highly collaborative with the team having a collective responsibility for the overall delivery.
The role is focused on supporting drug discovery projects within R&D Gothenburg by maintaining a high quality handling and storage of HBS and support projects with requested samples in a timely manner.

Responsibilities
As a Biobank Research Scientist you will be expected to:
-Work as part of the team rotating between the following typical tasks
-Receive and register incoming HBS
-Process requests for HBS to customers, including using automated liquid handler
-Manage customer orders using specialized informatics systems as well as databases
-Respond to customer queries via mail or telephone
-Partner with Biobank groups globally as well as internal and external customers
-Work closely with other groups in the organization
-Act upon day-to-day issues that occur whilst processing HBS samples to ensure continuous improvement
-Identify initiatives to improve efficiency or quality.

The group has a strong emphasis on continuous improvement which takes the form of individual and group projects within the team, the department and across Biobank groups within AZ.

The biobank team is a highly collaborative group working to tight delivery schedules so the ability to be comfortable working at a fast pace with a goal orientated and team focussed attitude is essential. Excellent communication skills with a proactive and service minded approach is key.

Your profile
• University degree in a Bioscience discipline and previous experience of laboratory work handling biological samples.
• Previous knowledge and experience (1 year) of biobanking is highly desirable.
• Experience of working with various IT solutions, including extensive knowledge of Excel, LIMS systems and database usage, is also a clear advantage.
• Experience of automated liquid handling is advantageous.
• Good analytical and problem-solving skills involving large and complex datasets is desirable.
• Excellent English, both spoken and written

• Ability to plan, perform and evaluate experiments to investigate improvement possibilities in a process.
• Knowledge of the regulatory framework of biological samples.
• Interest in logistics and developing processes through customer interactions and technology awareness.
• Drive and enthusiasm to solve the root cause of problems and not only overcome the presenting problem.
• Thrive on working in a committed team and gain satisfaction from the overall performance of the group

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for 8 months. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development. Visa mindre

Biobank scientists are responsible for the storage and timely supply of human biological samples (HBS) to AZ research projects. HBS are received from e.g. clinical studies or academic collaborations, stored in local biobanks and distributed to projects. The group primarily supports the Sweden Region but partners with other Biobank groups within the Biosamples department globally to provide efficient support across AZ and our partner organisations.

The Biobank group works collaboratively to provide support within agreed service levels with a strong focus on our customers. We strive hard to understand what fits their needs best and to add value through our services. With an increased focus on the value and use of biobank samples we actively seek ways to improve our process or exploit new technology to build a cutting edge facility.


About the position
We are currently recruiting for a temporary Biobank Scientist in the AZ Gothenburg Biobank group within the global Precision Medicine and Biosamples organization. This position will provide the opportunity to work in a dynamic and enthusiastic environment whilst supplying a critical service to drug discovery projects. The work is highly collaborative with the team having a collective responsibility for the overall delivery.
The role is focused on supporting drug discovery projects within R&D Gothenburg by maintaining a high quality handling and storage of HBS and support projects with requested samples in a timely manner.

Responsibilities
As a Biobank Research Scientist you will be expected to:
-Work as part of the team rotating between the following typical tasks
-Receive and register incoming HBS
-Process requests for HBS to customers, including using automated liquid handler
-Manage customer orders using specialized informatics systems as well as databases
-Respond to customer queries via mail or telephone
-Partner with Biobank groups globally as well as internal and external customers
-Work closely with other groups in the organization
-Act upon day-to-day issues that occur whilst processing HBS samples to ensure continuous improvement
-Identify initiatives to improve efficiency or quality.

The group has a strong emphasis on continuous improvement which takes the form of individual and group projects within the team, the department and across Biobank groups within AZ.

The biobank team is a highly collaborative group working to tight delivery schedules so the ability to be comfortable working at a fast pace with a goal orientated and team focussed attitude is essential. Excellent communication skills with a proactive and service minded approach is key.

Your profile
• University degree in a Bioscience discipline and previous experience of laboratory work handling biological samples.
• Previous knowledge and experience (1 year) of biobanking is highly desirable.
• Experience of working with various IT solutions, including extensive knowledge of Excel, LIMS systems and database usage, is also a clear advantage.
• Experience of automated liquid handling is advantageous.
• Good analytical and problem-solving skills involving large and complex datasets is desirable.
• Excellent English, both spoken and written

• Ability to plan, perform and evaluate experiments to investigate improvement possibilities in a process.
• Knowledge of the regulatory framework of biological samples.
• Interest in logistics and developing processes through customer interactions and technology awareness.
• Drive and enthusiasm to solve the root cause of problems and not only overcome the presenting problem.
• Thrive on working in a committed team and gain satisfaction from the overall performance of the group

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development. Visa mindre

About the position
Inhalation Product Development (IPD) at AstraZeneca is a multinational organization that combines decades of experience in inhalation technology whether it is nebulization, pMDI or DPI. Our vision is to develop and provide to patients best-in-class, innovative and sustainable products to deliver medicine via inhalation.

We are now seeking an Analytical Scientist to join our dynamic Analytical Sciences team, focusing on the characterization of inhaled molecules within Inhalation Product Development in Gothenburg. This is a unique opportunity to play a pivotal role in the development of inhaled products for AstraZeneca. You will be part of a highly collaborative team of analytical experts within the inhalation area, contributing to analytical development and characterization of inhaled products.

Responsibilities
This job includes lab-based responsibilities, where you are expected to work collaboratively with colleagues in daily analytical deliveries, documenting your experiments carefully and to the right quality, utilizing both manual and automated analytical techniques to develop and deliver innovative inhaled medicines to patients.

Your profile
Essential for the role:
• BSc or MSc degree in Analytical Chemistry or other relevant scientific discipline (Biochemistry, Biotechnology..).
• Scientific knowledge within analytical sciences and technically skilled with analytical separation techniques such as liquid chromatography (UPLC).
• Strong scientific interest and ambition to develop yourself in the analytical sciences area as well as leaning analytical techniques used for inhaled products.
• Excellent communication skills in English, both oral and written.
• Understanding the principles and applications of GMP.

Desirable for the role:
• Experience in aerosol characterization techniques used for inhaled products, such as impactor analysis.
• Experience of working in a GMP environment.
• Experience with method development and validation.
• Experience with solving technical challenges and problems.
• Experience of analysis of small molecules.

About the organisation
This is a consultant assignment at AstraZeneca in Göteborg until 2025-03-31. During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

Do you have organic synthesis expertise? Are you interested in becoming part of an impactful team passioned for science and technology, and focussed on chemistry automation to accelerate drug discovery? Would you like to become part of a company where we are committed to lifelong learning, growth, and development? This might be your next challenge!

We are looking for an Organic Chemist who will play an important part in our interdisciplinary team, implementing state-of-the-art chemistry automation technologies for the high-throughput synthesis of new molecules for projects.

About the position
By using chemistry automation technologies, you will contribute to the optimisation and synthesis of libraries of screening compounds (including traditional small molecules and small molecules degraders) on nanomol and micromol scale to progress projects. You will collaborate with experts in a variety of disciplines, including medicinal chemistry and artificial intelligence, to maximise the impact of our capabilities. You will contribute to the evaluation and development of automation-friendly synthetic methods to access optimal synthetic pathways for the synthesis of desired libraries and make a significant contribution to the team delivery.
You will have access to the best internal and external science and enhance business reputation internally and externally through peer-reviewed publications and oral/poster presentations.

Responsibilities
By using chemistry automation technologies, you will contribute to the optimisation and synthesis of libraries of screening compounds (including traditional small molecules and small molecules degraders) on nanomol and micromol scale to progress projects. You will collaborate with experts in a variety of disciplines, including medicinal chemistry and artificial intelligence, to maximise the impact of our capabilities. You will contribute to the evaluation and development of automation-friendly synthetic methods to access optimal synthetic pathways for the synthesis of desired libraries and make a significant contribution to the team delivery.
You will have access to the best internal and external science and enhance business reputation internally and externally through peer-reviewed publications and oral/poster presentations.

Your profile
You’re a chemist with a track record of applying innovative chemistry solutions, with resulting impact on project delivery. You also have:
• Ph.D. in organic chemistry, or a Master degree in chemistry with minimum 5 years’ experience in synthetic organic chemistry
• Experience in planning and executing chemistry experiments in parallel and adapting existing protocols to new applications
• Expertise in organic synthesis, retrosynthesis, compound route design, purification, and analytical chemistry
Experience in chemistry automation and plate chemistry would be desirable

The successful candidate should encourage innovation and be motivated to work effectively in team having strong communication and collaboration skills. The ideal candidate should demonstrate ability to work across scientific fields, possess a curious mind and a long-term commitment to advancing chemistry automation as an innovative tool in drug discovery.

About the organisation
This is a consultant assignment at AstraZeneca in Göteborg during the autumn 2024.
During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

Om tjänsten
Vill du spela en avgörande roll i vårt test-team på Volvo Penta? Vi söker en Test Equipment Engineer!

Den spännande rollen som Test Equipment Engineer (TEE) kommer du att vara nyckeln till att säkra effektiviteten i våra testceller och driva innovation inom marinmotorer och drivlinjeteknik. Tillsammans med oss kommer du att ansvara för provrummen, vilket innebär service, kalibrering och underhåll av utrustningen i våra testceller samt för inköp av instrument och reservdelar.

Dina arbetsuppgifter i huvudsak
Arbetsuppgifterna inkluderar bland annat:
– Säkerställa drifttid och effektiv arbetsplanering för testanläggningen.
– Hantera fel och problem genom problemlösning och dokumentation.
– Fokusera på att förbättra kvalitet och effektivitet i testningen.
– Samarbeta med andra team för att utveckla och uppfylla projekt- och lagkrav.
– Generera och följa upp statistik och KPI för att säkerställa effektivitet.
– Testa och godkänna ny utrustning innan användning.
– Driva referensmotorn för att säkerställa mätkvalitet och frigöra testceller.

Vem är du?
Krav för tjänsten:
– Universitetsutbildning inom elektroteknik och/eller mekanik eller motsvarande.
– Flytande i både skriftlig och talad engelska och svenska.
– Positiv, analytisk, strukturerad och med hög fokus på kvalitet och mätnoggrannhet.
– Självgående och ansvarsfull med en stark förmåga att kommunicera.

Meriterande för tjänsten:
– Erfarenhet från fordonsbranschen är meriterande.
– Erfarenhet av arbete med avgasutsläpp/testutrustning/kalibrering/MaintMaster är en fördel.
– Erfarenhet inom Comtest, RTP, Gantner, Siemens S7 och Tia Portal är också ett plus.

Om du tror att du är den positiva, serviceinriktade och engagerade lagspelaren som vi letar efter, säkra din ansökan idag. Vi ser fram emot att prata vidare och se om du är den perfekta matchen för tjänsten!

Om verksamheten
QRIOS kan erbjuda flera möjligheter till dig som är ingenjör eller har en teknisk bakgrund. Våra uppdragsgivare finns inom miljö-, energi-, skogs-, fordons-, läkemedels-, livsmedels-, process- och produktionsindustrin. Oavsett om du vill arbeta på ett stort eller litet företag, inom privat eller offentlig sektor, så har vi en tjänst för dig. Vi förenar människor och teknik!

Att vara konsult hos oss ger dig många möjligheter att prova på olika branscher, företag och roller. Läs gärna mer om hur det är att vara konsult hos oss: https://www.qrios.se/om-oss. Det passar dig som vill få mycket erfarenhet under en kortare period. Om du letar efter en värld fylld av spännande möjligheter och nya kontakter kommer du gilla att vara konsult hos oss. Visa mindre

Ansök via denna länk: https://www.sgi.se/sv/om-sgi/lediga-jobb/
Om arbetsplatsen
Statens geotekniska institut (SGI) är en expertmyndighet som arbetar för ett säkert, effektivt och hållbart byggande och ett hållbart användande av mark och naturresurser. I våra uppgifter ingår att förebygga jordskred, ras och stranderosion. SGI arbetar också med att ta fram nya metoder för att sanera förorenade områden. SGI tillhör Klimat- och näringslivsdepartementet och har totalt cirka 100 medarbetare. Huvudkontoret ligger i Linköping och kontor finns i Stockholm, Göteborg och Malmö.

Vi söker dig som har yrkeserfarenhet och som är intresserad av att arbeta med forskning och utveckling inom geoteknikområdet.

Våra medarbetare är vår viktigaste tillgång och för att kunna genomföra vårt samhällsuppdrag, behöver vi kunniga och engagerade medarbetare. Vi behöver även dra nytta av våra olikheter i bakgrund, erfarenhet och kompetens. Hos oss erbjuds du intressanta och varierande arbetsuppgifter som har stor betydelse för framtidens samhällsplanering.

Vi arbetar med såväl forskning som rådgivning och kunskapsförmedling för att bidra till en säker och hållbar samhällsutveckling. Detta gör vi bland annat genom att ge stöd till myndigheter och kommuner i geotekniska frågeställningar. Samhällets behov av stöd för att förebygga risker och förhindra skador vid naturolyckor som ras, skred och erosion har ökat och kommer ytterligare att öka till följd av exploatering och den pågående klimatförändringen. Vi ser därför en ökad efterfrågan av vårt stöd vad gäller geotekniska frågeställningar i bland annat planprocessen.
Arbetsuppgifter
Dina arbetsuppgifter består i huvudsak i att arbeta med tillämpad forskning och kunskapsförmedling inom geoteknikområdet samt att arbeta med stöd till kommuner och andra myndigheter i geotekniska frågeställningar. Forskning- och utvecklingsverksamheten är inriktad på att förbättra kunskapen om markens lämplighet för byggande, hur en minskad belastning på resurser och klimat i mark-
byggandet kan uppnås samt metoder och teknik som stödjer detta.

Vi arbetar med tillämpad forskning inom följande områden, geotekniska egenskaper hos jord samt effektivare grundläggnings- och förstärkningsmetoder för geotekniskt problematiska jordar samt ändrade lastförhållanden till följd av ett förändrat klimat.

I rollen ingår att bedriva forskning som skapar ett mervärde i genomförandet av vårt samhällsuppdrag samt arbeta för att resultaten från utförd forskning kommer till praktisk nytta. Du förväntas ta egna initiativ och aktivt bidra och ansvara för att ta fram nya utvecklings och forskningsansökningar som även bidrar till att skapa en externfinansiering för delar av verksamhetsområdets forskning. Utöver detta ingår också att bidra till samhällsnytta genom att publicera målgruppsanpassade vägledningar och praktiska rekommendationer.

Arbetet innebär, förutom att leda egna både interna och externa uppdrag, också att medverka i andras uppdrag inom SGI:s verksamhet. Du kommer att ha många externa kontakter med främst myndigheter och forskningsaktörer men också kontakter med kommuner och privata beställare.

Tjänsten innefattar även medverkan i vår verksamhet med kunskapsförmedling, exempelvis kurser, seminarier och föredrag. Den som anställs kommer att ingå i SGI:s beredskapsorganisation som geotekniskt stöd till framförallt räddningstjänsten när ras eller skred inträffat eller kan befaras (TiB tjänsteman i beredskap).
Kvalifikationer
Vi söker en erfaren geotekniker med civilingenjörsexamen från samhällsbyggnads- eller väg- och vattenbyggnadsprogrammet eller med relevant yrkeserfarenhet som arbetsgivaren bedömer lämplig. Meriterande för tjänsten är forskarutbildning och kompetens inom numerisk modellering, erfarenhet av att leda och genomföra stabilitetsutredningar samt erfarenhet av granskning av geotekniska handlingar.

Vi vill att du ska ha intresse för samhällets och geoteknikbranschens behov av utveckling. Du förväntas självständigt ta initiativ till nya uppdrag inom forsknings- och utvecklingsverksamhet samt kunna uttrycka dig väl i tal och skrift på både svenska och engelska. Det är viktigt att du finner glädje i externa kontakter, uppskattar samarbete och kan inspireras av vårt samhällsuppdrag.

Vid urvalet kommer stor vikt att läggas vid din personliga lämplighet. För att kunna arbeta hos oss ska du dela statens gemensamma värdegrund, http://www.sgi.se/sv/om-sgi/sa-arbetar-vi/vardegrund-och-kompass/
Kontaktpersoner
Helene Kennedy Avdelningschef 031 749 65 80, Mattias Andersson Enhetsansvarig 013- 20 18 88, Vi söker en eller flera medarbetare. Tjänsten är placerad vid enheten grundläggning, Avdelningen fysisk planering och byggbarhet, i Linköping, Göteborg eller Stockholm. Tjänsten är en tillsvidareanställning, men provanställning kan komma i fråga. Tillträde snarast enligt överenskommelse.
Ansök via denna länk till SGI´s hemsida: https://www.sgi.se/sv/om-sgi/lediga-jobb/ Visa mindre

Inhalation Product Development (IPD) at AstraZeneca is a multinational organization that combines decades of experience in inhalation technology whether it is nebulization, pMDI or DPI. Our vision is to develop and provide to patients best-in-class, innovative and sustainable products to deliver medicine via inhalation.

About the position
We are seeking an Analytical Scientist to join our dynamic Analytical Sciences team, focusing on the characterization of inhaled molecules within Inhalation Product Development in Gothenburg. This is a unique opportunity to play a pivotal role in the development of inhaled products for AstraZeneca. You will be part of a highly collaborative team of analytical experts within the inhalation area, contributing to analytical development and characterization of both small and large molecules.

Responsibilities
This job includes lab-based responsibilities, where you are expected to work collaboratively with colleagues in daily analytical deliveries, utilizing both manual and automated analytical techniques to develop and deliver innovative inhaled medicines to patients.
You will apply your analytical expertise with large and/or small molecules to specific drug projects, contributing to the analytical development and strategy within the inhaled project.
You will be contributing significantly to Chemistry, Manufacturing, Control (CMC) aspects in the project, working closely with formulation scientists, device engineers, biopharmaceutic and process engineers in IPD Gothenburg as well as globally with the colleagues in IPD North Carolina.
To be successful in this role you will need a strong analytical background in working with different types of molecules combined with excellent communication skills and the ability to engage and collaborate cross-functionally. We are looking for a candidate that possesses a fair understanding of the overall drug development process and has an enthusiasm for laboratory-based work as well as solving technical challenges and problems.

Your profile
-Degree in Analytical Chemistry or other relevant scientific discipline (Biochemistry, Biotechnology). (PhD or Bsc/Msc with extensive experience).
-Experience with analytical separation techniques such as liquid chromatography (UPLC) for large and/or small molecules. If experience with large molecules it would also be beneficial. Proficiency in method development and validation of analytical methods. Experience with analytical methodologies for oligonucleotides, peptide and proteins characterisation (e.g., capillary electrophoresis, ion-exchange chromatography, ELISA, SDS-PAGE) is highly desirable.
-Strong data analysis skills, with the ability to interpret results and communicate findings effectively to stakeholders and along with proven ability to solve technical challenges and problems. Insights into the use of statistical analysis software would be great. Familiarity with working and communicating within a global, cross-functional project environment is desirable. Understanding of analytical development work and CMC deliveries projects.
Experience working in a GMP environment and knowledge of corresponding instrument/equipment maintenance procedures as well as knowledge of the overall drug development process from discovery through to launch would be beneficial. Experience in aerosol characterization techniques used for inhaled products, such as impactor analysis would be a bonus.
-Excellent communication skills in English, both oral and written.

About the organisation
This is a consultant assignement for one year at AstraZeneca in Gothenburg. Start day depends on when it is suitable for the candidate. During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives – and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

Ansök via denna länk: https://www.sgi.se/sv/om-sgi/lediga-jobb/
Om arbetsplatsen
Statens geotekniska institut (SGI) är en expertmyndighet som arbetar för ett säkert, effektivt och hållbart byggande och ett hållbart användande av mark och naturresurser. I våra uppgifter ingår att förebygga jordskred, ras och stranderosion. SGI arbetar också med att ta fram nya metoder för att sanera förorenade områden. SGI tillhör Klimat- och näringslivsdepartementet och har totalt cirka 100 medarbetare. Huvudkontoret ligger i Linköping och kontor finns i Stockholm, Göteborg och Malmö.
Göta älvdalen är Sveriges mest skredbenägna region och samtidigt det område som bedöms påverkas mest av klimatförändringen framöver. Framtida skred skulle påverka både samhällsviktiga funktioner, riksintressen, Natura2000-områden och inte minst många som bor i Göta älvdalen.
Som geotekniker i sekretariatet för Göta älv får du möjlighet att minska riskerna i denna region, du kan göra skillnad, som är till nytta för hela samhället!
Arbetsuppgifter
Det är ett välfinansierat regeringsuppdrag som möjliggör att SGI kan arbeta enligt nya utredningsmetoder med projekt från behovsanalys och fram till färdig åtgärd, optimerad enligt den senaste kunskapen. Här blir du del av en engagerad och prestigelös projektgrupp som drivs av att förbättra förutsättningarna för de som bor och verkar längs Göta älv och samtidigt fördjupa sin kunskap inom geotekniska frågeställningar.
Du kommer att leda stabilitetsutredningar samt stötta våra kommuner i deras projektering och under åtgärdsfasen med stöd från kompetenta kollegor. Arbetet innebär många kontakter, både internt och externt. Hos oss får du arbeta med helheten, Göta älv från Vänersborg till Göteborg är ett stort projekt. Sekretariatet har tillgång till en stor mängd undersökningsresultat. Såväl geotekniska beräkningsverktyg som GIS-program används i hög grad. I arbetet ingår att vara en del av SGI:s beredskapsorganisation som geotekniskt stöd till framför allt räddningstjänsten i händelse av eller vid tidiga indikationer på ras eller skred.
Kvalifikationer
Tjänsten kräver universitets- eller högskoleutbildning: civilingenjör (exempelvis väg och vatten eller samhällsbyggnad) eller liknande utbildning som av arbetsgivaren bedöms vara lämplig för tjänsten. För arbetet krävs goda geotekniska kunskaper, särskilt inom området släntstabilitet. Du bör ha erfarenhet av geotekniskt utredningsarbete samt projektering.
Vi löser våra uppdrag tillsammans, vilket innebär att du bör tycka om att jobba i grupp/team och att dela med dig av erfarenheter. Du ska kunna uttrycka dig väl i tal och skrift på svenska. Du har mycket god datavana och arbetar väl i Microsoft- Officepaket.
Vid urvalet kommer det att läggas stor vikt vid din personliga lämplighet. För att kunna arbeta hos oss ska du dela statens gemensamma värdegrund, http://www.sgi.se/sv/om-sgi/sa-arbetar-vi/vardegrund-och-kompass/
Vi erbjuder
Vi erbjuder dig ett samhällsviktigt uppdrag, spännande och utvecklande arbetsuppgifter med generös syn på kompetensutveckling samt en trevlig arbetsplats med medarbetare i fokus med stort engagemang och arbetsglädje. Vi har generöst med semesterdagar, möjlighet att till viss del arbeta på distans, individuell lön, flexibel arbetstid, friskvårdsbidrag, m.m.
Kontakt
Kontaktpersoner
Per Bolin, Chef för Delegationen för Göta älv, Telefon 031- 7496595
Fackliga företrädare för Saco
Martin Holmén Telefon 013 201815 ellerAdnan Drobic Telefon 031-7786572
För ST Eva Albin Telefon 013-20 18 29 eller Oskar Alm Telefon 013-201825
Övrigt
Andra placeringsorter än Göteborg kan eventuellt diskuteras. Tjänsten är en tillsvidareanställning, men provanställning kan komma i fråga. Tillträde snarast enligt överenskommelse. Visa mindre

Do you have hands-on experience with the purification of small molecules? Are you interested to further push the boundaries of automated analytical chemistry and separation sciences at a company where we are committed to lifelong learning, growth and development? Welcome to AstraZeneca!

We are seeking a specialized separation scientist that will play an important part in our iLAB team, focusing on the analysis and purification of chemical libraries. You’ll have the opportunity to drive and extend the high-throughput purification capabilities within a pioneering automation platform at AstraZeneca in Gothenburg and directly impact drug discovery projects across various therapeutic areas.

About the position
As Separation Scientist, you will be part of a team of highly motivated scientists contributing to analysis, preparative separation, and characterisation of small molecule chemical libraries.
In this laboratory-based position, you will be specifically responsible for ensuring the delivery of automated analytical and preparative chromatography solutions to drive the delivery of pure compounds to the different projects across our therapy areas within AstraZeneca. You will get the opportunity to work with state-of-the-art chromatographic equipment and liquid handlers.
You will be expected to have effective levels of communication and scientific drive, coordinating effectively with the other members of the analytical and synthesis teams to drive sample progression.

Experience and technical knowledge of chromatographic separations within a drug discovery environment would be an advantage.

Responsibilities
• Provide hands-on separation science support to drug discovery chemistry using state-of-the art chromatographic instrumentation
• Deliver automated analysis and purification of novel compounds using Liquid chromatography–mass spectrometry (LC–MS) and High-performance liquid chromatography (HPLC)
• Ensure reliability, performance and data quality of analytical instrumentation and automation platforms
• Work within the team to suggest process and infrastructure improvements
• Contribute to a vibrant and entrepreneurial organization focused on innovation & project delivery; collaborating closely with scientists across the discovery organization

Your profile
You’re a separation scientist with a track record of applying innovative analytical chemistry solutions. You also have:

• BSc/MSc in Chemistry or Analytical Chemistry
• Good knowledge of analytical and/or preparative chromatographic techniques (HPLC, HPLC-MS) including method development and instrument troubleshooting
• Lab-based experience using analytical chemistry and/or automation techniques.
• Detailed understanding of the use of analytical techniques to solve complex scientific questions.
• Ability to work in multidisciplinary team / project / function.
• Excellent communication skills
• First-rate time management skills, forward planning, and delivery focus, leading to good team working and a high level of self and team delivery.

About the organisation
This is a consultant assignement for one year at AstraZeneca in Gothenburg. Start day depends on when it is suitable for the candidate. During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives – and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

About the position
We now offer a unique opportunity for senior scientist with great skills in peptide chemistry and with a special interest in bridging novel synthetic chemistry and medicinal chemistry in design of drug modalities and conjugates. Join our experienced team in New Modalities drug discovery and contribute with your high ambitions, collaborative mindset and enthusiasm. The position is placed at AstraZeneca’s dynamic R&D site in Gothenburg, Sweden.

Responsibilities
The role is fully lab based and focused on synthetic chemistry of various modalities and drug conjugates, in particular peptide chemistry
You will actively contribute to compound design and synthesis, analysis, purification, data generation and data interpretation.
The person will need to be skilled in both oligonucleotide synthesis, oligo building block synthesis and oligo conjugate synthesis and has to have hands on experience with several oligo instruments.

Your profile
Essential for the role
We are looking for an ambitious team player that have expert knowledge in synthetic organic chemistry applied across multiple modalities and handling of complex molecules.
• Ph. D. degree in Organic Chemistry, Medicinal Chemistry, Chemical Biology with emphasis on peptide synthesis and oligonucleotide synthesis.
• Synthetic chemistry: ability to plan, prioritize and perform work independently including synthetic route design and problem solving
• Awareness of recent literature as well as current developments and trends in organic synthesis
• Highly self-motivated and capable of analyzing complex data and deciding on focused course of action
• Excellent teamwork, collaboration, networking and communication skills

About the organisation
This is a consultant assignement for one year at AstraZeneca in Gothenburg. Start day depends on when it is suitable for the candidate. During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives – and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

We are currently looking for a laboratory skilled Scientist to join the Bioscience COPD IPF Department within Early Respiratory and Immunology (R&I). This role is located in Gothenburg, Sweden.
The Bioscience COPD/IPF department consist of 7 teams spread across Sweden, UK and US and our focus is primarily to progress projects within our portfolio, but it also includes work to increase our knowledge of COPD and IPF and to support target identification for new projects.

About the position
As a Scientist you will plan, optimise, and execute in vitro experiments as well as support analysis from both in vitro and in vivo studies to progress our drug discovery projects and generate publishable scientific insights. You are expected to actively take part in scientific discussions and to add valuable input in experiment design and data interpretation to drive projects and techniques.
This is a lab-based role where you will be involved in multiple ongoing projects with responsibility to perform experiments from various cells and tissues for both in vitro-, in vivo- and patient studies. This role will give the opportunity to support, design, develop and conduct experiments supporting the identification of new drug targets and the progression of drug discovery projects.
For this role, we are looking for someone with experience in modern cell biology and molecular analysis techniques that rapidly can become an integrated project member and deliver key data.

Responsibilities
We will rely on you to:
• Execute in vitro/ex vivo experiments according to study plans
• Contribute to the interpretation of experimental data and play an important role in the planning of further experiments
• Effectively communicate results to other members of the project, team or to departments as required
• Be an effective team member in supporting projects to meet their objectives
• To conduct where appropriate in parallel more than one area of work to agreed timelines
• Possess a range of practical skills and demonstrate flexibility within and across teams

Your profile
Essential requirements:
-A relevant science degree (MSc or BSc) ( e.g Molecular/Cell Biology, Pharmacy, Biotechnology)
-Practical experience running in vitro assays and cell culturing
Relevant experimental experience in cell and molecular biology methods, immunoassays, protein and RNA analysis
-Isolation, culturing and analysis of primary cell cultures along with experience in the use of biological dose response assays is desirable. Experience in immunological methods (ELISA, MSD), protein analysis (western blot) and RNA analysis (qPCR) plus handling and evaluation of pharmacological drug substances would also be benificial.
- Excellent written and oral communication skills in English is a must

Soft skills:
You also possess great problem-solving skills. You have a positive and goal-oriented attitude, and you are a team player but are also able to take your own initiatives. You are organized and incorporate the views of others in your communication and collaboration.

About the organisation
This is a consultant assignement for one year at AstraZeneca in Gothenburg. Start day depends on when it is suitable for the candidate. During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives – and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

Om arbetsplatsen
Statens geotekniska institut (SGI) är en expertmyndighet som arbetar för ett säkert, effektivt och hållbart byggande och ett hållbart användande av mark och naturresurser. I våra uppgifter ingår att förebygga jordskred, ras och stranderosion. SGI arbetar också med att ta fram nya metoder för att sanera förorenade områden. SGI tillhör Klimat- och näringslivsdepartementet och har totalt cirka 100 medarbetare. Huvudkontoret ligger i Linköping och kontor finns i Stockholm, Göteborg och Malmö.

Vi erbjuder dig
Att jobba på en myndighet ger unika möjligheter att både ta del av och påverka pågående samhällsutveckling och själv vara aktiv i att bedriva forskning och utveckling för att skapa förbättringar. Hos SGI finner du en kreativ miljö med många olika kompetenser inom organisationen. Ett tydligt samhällsansvar och goda förutsättningar att skapa samhällsnytta stimulerar våra medarbetares engagemang.
Arbetsuppgifter
För att kunna bygga på och i berg på ett planerat och hållbart sätt behöver samhället förbättrad kompetens och kunskap om bergets egenskaper för byggnation. Genom att leda utveckling med kunskapsuppbyggnad och vägledningar inom detta område bedöms SGI kunna göra stor samhällsnytta och vill därför nu stärka vår kompetens med en erfaren ingenjörsgeolog.

Du kommer att ha en viktig roll i SGI:s utvecklingsarbete för att stötta samhället med kunskap och vägledning för en effektiv och hållbar planering och byggprocess i berg. Tillsammans med kollegor ges du möjlighet att arbeta med följande frågor:
• Stödja SGI:s uppdrag inom våra tre verksamhetsområden: Effektivare markbyggande, Klimatanpassning och renare mark, där frågor kopplade till berg är aktuella.
• Identifiera och analysera risker kopplade till ras, skred och erosion.
• Stödja SGI:s verksamhet som remissinstans.
• Arbete med förbättrad undersökningsmetodik för att provta och analysera berggrundens geotekniska egenskaper.
• Förmedla kunskap via kurser, konferenser och seminarier.
• Initiera forskning och driva utveckling inom ämnesområdet, där så är lämpligt i samverkan med andra myndigheter, universitet, högskolor och företag.
Kvalifikationer
Vi söker dig med högskoleexamen eller motsvarande utbildning samt med gedigen relevant arbetslivserfarenhet. Du bör ha djup kunskap om de genetiska processer som skapat dagens förhållande för byggnation i berg. Du vill hjälpa samhället och oss här på SGI att utveckla ingenjörsgeologin i Sverige bland annat genom forskning, metodutveckling och framtagande av vägledningar.

För tjänsten krävs att du som sökande har god dokumenterad kunskap inom följande områden:
• Ingenjörsgeologiska undersökningar och karaktärisering av bergs fysikaliska egenskaper
• Geologiska bildningsprocesser, särskilt med hänsyn till berggrundens svaga och porösa strukturer
• Uppdragsledning

Meriterande är praktisk erfarenhet av anläggningsprojekt i berg samt akademiska meriter.
Vi vill att du är noggrann och strukturerad i ditt arbetssätt. Du tar egna initiativ, är lösningsorienterad och har en förmåga att kunna se både det stora och det lilla perspektivet. För rollen krävs en god förmåga att uttrycka sig i tal och skrift på svenska.

Vid urvalet kommer stor vikt att läggas vid din personliga lämplighet och det är viktigt att du har en god samarbetsförmåga. Vi ser gärna att du inspireras av vårt samhällsuppdrag och för att kunna arbeta hos oss ska du dela statens gemensamma värdegrund, http://www.sgi.se/sv/om-sgi/sa-arbetar-vi/vardegrund-och-kompass/
Anställningsform : Tillsvidareanställning på heltid
Kontaktpersoner: Johan Berglund,Berggrundsgeolog 031 7786562, Mats Eriksson, Avdelningschef Georisker och geodata 08 57845519
Fackliga företrädare: Martin Holmén SACO 013 201815, Eva Albin ST, 013-20 18 29
Övrigt
Välkommen med din ansökan via denna länk: https://www.sgi.se/sv/om-sgi/lediga-jobb/ Visa mindre

We now have the opportunity for a consultant to join our team in the roles as Senior Scientist Pharmaceutical/Senior Analytical scientists within the Analytical Science Unit in the department Oral Product Development at AstraZeneca Gothenburg.

About the position
We are looking for a senior scientist in Analytical Chemistry who can provide input in the area of analytical science during the development of drug products and can work together with us determining the quality attributes during the development of the formulations. The work includes analytical testing , documentation, and attending and presenting in project team meetings. The role is primarily laboratory based.

Your profile
To be successful in this role you will need expertise in analytical chemistry and an experience from laboratory work.
- Excellent skills in written and verbal communication and the ability to engage and collaborate across boundaries with a positive problem-solving attitude and delivery focus.
- University degree (BSc, MSc, PhD) in relevant subject area, with industry experience
- Experience from working with chromatography and other techniques e.g. HPLC/UPLC, and dissolution, both in a GxP and a non GxP environment
- Experience of supporting clinical manufacture and working with contract manufacturing organisations
- Experience of authoring CMC content for the analytical aspects of drug product regulatory filings throughout the clinical development phase
- Experience of the analytical area such as method development and method validation.
- Experience from evaluation of stability data and assigning shelf life to drug products
- Excellent communication skills and a proven track record of working collaboratively to develop innovative solutions
- Strong leadership skills including the ability to deliver robust scientific contributions to projects and utilise risk-based approaches to project delivery
- Good knowledge in written and spoken Swedish and/or English is necessary

About the organisation
This is a consultant assignement from August until end of December 2024 at AstraZeneca Göteborg.
During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives – and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

About the position
We are now looking for a Scientist to join the In vivo Bioscience team within Research and Early Development, Respiratory & Immunology in Gothenburg, Sweden.

Respiratory & Immunology is one of AstraZeneca’s main therapy areas. From a research perspective we work to understand, treat, modify and ultimately cure respiratory and autoimmune diseases. In this role, you will focus on mouse models of inflammatory bowel disease (IBD).

Responsibilities
As part of the team, you will plan, execute and analyse ex vivo samples generated from in vivo studies to progress our drug discovery projects and generate publishable scientific insights. You will actively take part in scientific discussions to add valuable inputs in experimental design and data interpretation.

This is a mainly lab-based role where you will be involved in ongoing projects focusing on pre-clinical experiments.

What you’ll do:

• As a Scientist you will be a vital member of the in vivo community and will contribute to the development and characterization of pre-clinical models of IBD to discover novel therapeutics.
• You will contribute to the analysis of in vivo studies with a specific focus on FACS analysis.

Your profile
• At last 5 years of experience with regular FACS analysis of mouse samples (organ processing and digestion, cell staining, antibody panel set up, proficient in the use of BD FACS DIVA machines and Flowjo).
• Ability to organize, execute and interpret the results from in vivo studies according to study plans in agreement with the team leader or other colleagues.
• Experience with other in vitro methodology in addition to FACS (ELISA/MSD and/or qRT-PCR) to analyze ex vivo samples generated from in vivo studies.
• Experience of maintaining the highest standards of welfare and ethical compliance and ensuring the integrity of the generated data. Familiar with using Good Statistical Practice in animal research and applying the 3R’s (reduction, refinement and replacement) across the full range of studies.
• Valid education required for compliance to work with live animals in Sweden.
• Excellent English written and oral communication skills, including presentation skills.

Desirable for the role:

• Degree in immunology (master or PHD) and understanding of autoimmune diseases with a specific focus on gut immunology.
• Several years of hands-on experience with rodents including live animal handling, drug administration through different routes (i.v, i.p., p.o.), blood and organ sampling and processing (colon, small intestine, spleen, lymph nodes).
• Experience with animal models of inflammatory bowel disease (IBD) and in vivo PK/PD relationships.

About the organisation
This is a consultant assignement from August until end of December 2024 at AstraZeneca Göteborg.
During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives – and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

About the position
We now have the opportunity for one or several consultants to join our team in the role as Formulation Scientist/Product Developer within the department Oral Product Development at AstraZeneca in Gothenburg. The assignment is on a temporary basis.

Responsibilities
We are looking for a formulation scientist who can work together with us with generating and evaluating pharmaceutical technologies and formulations. The work includes development, characterization, and documentation, mainly of solid based formulations, in order to develop drug products.

The tasks include planning and implementation of experiments with the aim of generating new formulations and optimizing processes in lab and pilot scale. We are looking for both people with and without previous experience in the area.

Your profile
MSc/BSc in chemistry, pharmacy, chemical engineering, food technology or equivalent. Good knowledge in written and spoken Swedish and/or English is necessary as well as laboratory experience including working with computerized systems. If you have experience from working within the pharmaceutical industry, medical tech, or with manufacturing equipment, this will be an advantage. Solid materials/formulation experience is highly meriting.

As a person, you should be well organized, analytical, flexible and accurate. Good team working skills are also important, together with the ability to operate independently. Good communication skills linked to the ability to work to tight timelines are highly valued.

About the organisation
This is a consultant assignement from August until end of December 2024 at AstraZeneca Göteborg.
During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives – and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

About the position
APNC is an expanding company specializing in providing statistical solutions for life science research. Our clients are primarily medical researchers in academia, and pharmaceutical and medical technology companies. With a diversified client base, we offer stability and ample opportunities for growth. At APNC Sweden, each individual shapes the company as delegated responsibilities and leadership create the most favorable work environment. Our goal is to be as attractive employer as possible, both to attract and retain the very best employees and to contribute to their well-being and satisfaction. We offer benefits such as bonuses, flexible working hours and part-time options, opportunities for remote work, maximum health support, as well as healthcare and pension insurance. Our ambition is to promote continuous learning through various lectures, courses, and other skill development opportunities.

Responsibilities
We are currently seeking a Senior Statistician to join our growing team, which currently consists of 7 individuals with diverse backgrounds in statistics, biostatistics and programming. Our office is located in Mölndal, within the new, ever-growing life science cluster GoCo Health Innovation City. We are looking for an experienced statistician with a strong passion for medical research and the ability to collaborate and lead a team. Personality is key to meeting our clients and driving the continued development of the company.

Responsibilities:
• Planning and designing clinical studies
• Leading statistical analysis and programming
• Reporting and interpretation of results (study reports/publications)
• Collaboration with various roles, such as programmers, project managers, medical specialists, and regulatory experts
• Team leadership


Your profile
• University degree in statistics, mathematical statistics, or mathematics
• At least 5 years of experience working with statistics in medical research
• Solid experience in SAS/R/python
• Positive and problem-solving attitude
• Excellent communication and collaboration skills
• Experience in leading a team

About the organisation
We are collaborating with QRIOS Life Science & Engineering regarding this recruitment. The selection is ongoing, so be sure to send in your application today! Visa mindre

About the position
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.

Research Scientist position – in vitro cellular profiling
We are looking for a passionate Research Scientist to join our Mechanistic and Structural Biology department within the Discovery Sciences organization in Gothenburg, Sweden. You will apply your proven cell biology expertise to in vitro cellular assays. Routine profiling will be combined with tailored mechanism of action studies in cellular models across a multitude of different drug discovery projects. You will build a detailed understanding of the impact of treatment by multiple drug modalities, including small molecules, PROTACS and therapeutic oligonucleotides.
You will demonstrate a passion for applied science, combined with a strong emphasis on team work. You will join a team whose remit is to support our drug discovery projects globally with early DMPK assessment, SAR profiling and detailed mechanism of action data. We offer a highly rewarding scientific environment with ample learning opportunities.
You will be strongly encouraged and supported to think creatively in our dynamic environment. Here, we are free from fear of failure, free to ask the right questions and make bold decisions.

Responsibilities
What you will do:
This is a lab-based role focused on generating routine screening data and bespoke in vitro pharmacology studies in support of drug discovery projects. The work includes independent troubleshooting and timely reporting of data according to agreed timelines. All work is conducted in close dialog with project teams, specifically in support of the Cardiovascular, Renal and Metabolism as well as Respiratory & Immunology disease area organisations locally in Gothenburg.

Your profile
Essential to the role and desirable skills:

-MSc or PhD within a relevant scientific discipline or demonstrated relevant experience in the Life Science industry.
-Proven track record of cellular biology techniques and pharmacology studies.
-Compound profiling in a screening environment using microtiter plates and automation as well as experience in the design, development and validation of biological test assays for compound profiling.
-Practical knowledge of high-resolution MS for targeted or global proteomics analysis and several technology platforms such as imaging, flow cytometry and LC-MS
-Good knowledge of oral and written English is a requirement

Soft skills:
Excellent communication skills and an ability to operate effectively in a multi-disciplinary research environment.
Independent analysis and evaluation of complex data and delivery of data to agreed timelines.
First-rate decision-making skills, coupled with tenacity to see decisions through, even in situations of ambiguity.

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

About the position
Quality Assurance Advisor AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we're more than one of the world's leading pharmaceutical companies.

At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. The arena Are you interested in a challenging opportunity within the Development Quality function in one of the world’s leading pharmaceutical companies. The Development Quality function is responsible for quality oversight of the pharmaceutical development activities in AstraZeneca.

Responsibilities
We are now looking for a Quality Advisor with GMP focus to our Gothenburg team. AstraZeneca’s pharmaceutical development organizations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase. The role As a Quality Advisor, you will work with early product development manufacturing and packaging teams and be responsible for Development Quality release of externally manufactured Drug Product and Investigational Medicinal Product for clinical trials. You are expected to assure that activities and processes across the development chain are delivered to appropriate standards to meet regulatory expectations and assure product integrity and acceptability. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting. In your role you will have interactions with internal and external stakeholders.

Typical Accountabilities:

• Responsible for quality Release of manufactured Drug Product, Investigational Medicinal Product for clinical trials
• Providing quality input to Manufacturing, Packaging, Labelling & Distribution activities
• Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards
• Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects
• Provide appropriate Quality Assurance input to business improvement projects
• Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working.

Your profile
Requirements:

• Degree in pharmacy or engineering (specializing in Pharmaceuticals)
• 3 years’ experience of working within a pharmaceutical GMP environment
• Broad understanding of Quality Systems and GMP and related activities to Investigational Medicinal Product (IMP)
• Fluent in written and spoken English
• Experience of documentation, deviations, changes, and other quality and compliance decisions in the development projects.

Desirable:
• Experience preferably within a pharmaceutical manufacturing organization is desirable
• Understanding of Project Management processes
• Good team working and networking skills
• Capable of making effective decisions
• Demonstrate drive and energy in the role to make a difference
• Demonstrate a high degree of personal credibility
• Good communicator with experience of interacting effectively across interfaces.
• Comprehensive understanding of the pharmaceutical/drug development process

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

Jag söker efter en konsult för ett heltidsuppdrag hos en myndighet i Göteborg under perioden 2024-06-24 fram till 2024-08-09.
Konsulten kommer att omfattas av bestämmelserna i offentlighets- och sekretesslagen (2009:400), OSL. Konsulten kommer att få skriva under en sekretesserinran innan uppdraget påbörjas.

Dina arbetsuppgifter i huvudsak
Myndigheten vägleder kommunerna om skötsel av EU-bad i Sverige, rapporterar badvattendirektivet till Europeiska kommissionen och är värd för webbplatsen Badplatsen.

Under sommaren behöver myndigheten förstärka personalstyrkan och söker efter en sommararbetare som har en naturvetenskaplig bakgrund samt erfarenhet av att jobba serviceinriktat.
Uppdraget pågår upp till 7 veckors heltidsarbete förlagda över kontorstid: måndag till fredag. Trycket på arbetsuppgifterna varierar beroende av väder och badvilja. Huvudsakligen görs vägledningen via mejl, men sker också över telefon.

• Löpande ge vägledning runt badvatten till kommuner och allmänhet
• Löpande följa upp rapportering till webbplatsen Badplatsen
• Löpande hantera användarkonton för webbplatsen Badplatsen
• Löpande bidra till arbetet med utredningar och sammanställningar kring badvattenfrågor som uppkommer under
badsäsongen.

Du utför uppdraget i nära samarbete med medarbetare i myndighetens badvattengrupp, och interna beställare.

Vem är du?
• Högskole- eller universitetsexamen om minst 3 år med inriktning på akvatisk ekologi eller vattenvård.
• Andra möjliga inriktningar på utbildning är miljövetarprogrammet, samhällsvetenskapligt miljövetarprogram och biologiprogrammet.

• Du får gärna ha relevant erfarenhet inom t.ex. vattenförvaltning, miljökommunikation, miljöövervakning, digitalisering, arbete inom databaser, relevanta mikrobiologiska analyser, föroreningar av ytvatten, algblomning.

• God kommunikationsförmåga, serviceinriktad, självständig, stresstålig, lättlärd.

About the organisation
Detta är ett konsultuppdrag under perioden 2024-06-24 fram till 2024-08-09.
Under tiden som uppdraget är, så kommer du vara anställd av QRIOS.

Urval och intervjuer kommer ske löpande. Vänligen sök snarast. Visa mindre

Om arbetsplatsen
Statens geotekniska institut (SGI) är en expertmyndighet som arbetar för ett säkert, effektivt och hållbart byggande och ett hållbart användande av mark och naturresurser. I våra uppgifter ingår att förebygga jordskred, ras och stranderosion. SGI arbetar också med att ta fram nya metoder för att sanera förorenade områden. SGI tillhör Klimat- och näringslivsdepartementet och har totalt cirka 100 medarbetare. Huvudkontoret ligger i Linköping och kontor finns i Stockholm, Göteborg och Malmö.

Vi erbjuder dig
Att jobba på en myndighet ger unika möjligheter att både ta del av och påverka pågående samhällsutveckling och själv vara aktiv i att bedriva forskning och utveckling för att skapa förbättringar. Hos SGI finner du en kreativ miljö med många olika kompetenser inom organisationen. Ett tydligt samhällsansvar och goda förutsättningar att skapa samhällsnytta stimulerar våra medarbetares engagemang.
Arbetsuppgifter
För att kunna bygga på och i berg på ett planerat och hållbart sätt behöver samhället förbättrad kompetens och kunskap om bergets egenskaper för byggnation. Genom att leda utveckling med kunskapsuppbyggnad och vägledningar inom detta område bedöms SGI kunna göra stor samhällsnytta och vill därför nu stärka vår kompetens med en erfaren ingenjörsgeolog.

Du kommer att ha en viktig roll i SGI:s utvecklingsarbete för att stötta samhället med kunskap och vägledning för en effektiv och hållbar planering och byggprocess i berg. Tillsammans med kollegor ges du möjlighet att arbeta med följande frågor:
• Stödja SGI:s uppdrag inom våra tre verksamhetsområden: Effektivare markbyggande, Klimatanpassning och renare mark, där frågor kopplade till berg är aktuella.
• Identifiera och analysera risker kopplade till ras, skred och erosion.
• Stödja SGI:s verksamhet som remissinstans.
• Arbete med förbättrad undersökningsmetodik för att provta och analysera berggrundens geotekniska egenskaper.
• Förmedla kunskap via kurser, konferenser och seminarier.
• Initiera forskning och driva utveckling inom ämnesområdet, där så är lämpligt i samverkan med andra myndigheter, universitet, högskolor och företag.
Kvalifikationer
Vi söker dig med högskoleexamen eller motsvarande utbildning samt med gedigen relevant arbetslivserfarenhet. Du bör ha djup kunskap om de genetiska processer som skapat dagens förhållande för byggnation i berg. Du vill hjälpa samhället och oss här på SGI att utveckla ingenjörsgeologin i Sverige bland annat genom forskning, metodutveckling och framtagande av vägledningar.

För tjänsten krävs att du som sökande har god dokumenterad kunskap inom följande områden:
• Ingenjörsgeologiska undersökningar och karaktärisering av bergs fysikaliska egenskaper
• Geologiska bildningsprocesser, särskilt med hänsyn till berggrundens svaga och porösa strukturer
• Uppdragsledning

Meriterande är praktisk erfarenhet av anläggningsprojekt i berg samt akademiska meriter.
Vi vill att du är noggrann och strukturerad i ditt arbetssätt. Du tar egna initiativ, är lösningsorienterad och har en förmåga att kunna se både det stora och det lilla perspektivet. För rollen krävs en god förmåga att uttrycka sig i tal och skrift på svenska.

Vid urvalet kommer stor vikt att läggas vid din personliga lämplighet och det är viktigt att du har en god samarbetsförmåga. Vi ser gärna att du inspireras av vårt samhällsuppdrag och för att kunna arbeta hos oss ska du dela statens gemensamma värdegrund, http://www.sgi.se/sv/om-sgi/sa-arbetar-vi/vardegrund-och-kompass/
Anställningsform : Tillsvidareanställning på heltid
Kontaktpersoner: Johan Berglund,Berggrundsgeolog 031 7786562, Mats Eriksson, Avdelningschef Georisker och geodata 08 57845519
Fackliga företrädare: Martin Holmén SACO 013 201815, Eva Albin ST, 013-20 18 29
Övrigt
Välkommen med din ansökan till SGI.se Visa mindre

About the position
At AstraZeneca we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.

Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) across all the AstraZeneca therapy areas.
Our vision is to be “pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future”.
We’re looking for talented and motivated analytical chemist to join one of our analytical characterization teams within Early Product Development and Manufacturing (EPDM) in Gothenburg.

Responsibilities
You would join a highly collaborative team and together we will deliver the analytical science to product development within the early portfolio up to phase II.
To be successful in this role you will need a strong scientific background with good skills in written and verbal communication and the ability to engage and collaborate across boundaries with a positive problem-solving attitude and delivery focus.
This is a lab-based role where you will work collaboratively with colleagues, documenting your experiments carefully and to the right quality. You will get the opportunity to apply your excellent analytical expertise to the drug projects you are working in, contributing to the progression of these projects and drive the scientific development within the field of analytical science at AstraZeneca.

Your profile
Required Qualifications, Skills and Experience:
-University degree (MSc, PhD) in relevant discipline, preferable with industry experience
-Scientific knowledge within analytical science and technically skilled to use chromatography with relevant detection techniques for small molecules
-You are a driven experimentalist, with a passion to deliver highly relevant and reliable data and with the ability to be influential in discussions in a wide set of communities and multi-disciplinary project teams
-Excellent communication, collaboration, networking and leadership skills & ability to lead and inspire colleagues

If you also have experience in one or more of the following areas – great!
-Industry experience of pharmaceutical development including oral solid dosage form development
-Experience of CMC submissions and work according to GMP
-Skilled in specific analytical techniques for small molecules, e.g. mass spectrometry, NMR, dissolution etc
-Track record and keen interest of driving development within analytical science including championing new technologies and solutions

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

Ansök via denna länk
https://recruit.visma.com/spa/sv/public/apply?guidAssignment=ea846e08-0025-496c-87bf-ee7987077ce5&description=True&forcelocale=true
Om Arbetsplatsen
Statens geotekniska institut (SGI) är en expertmyndighet som arbetar för ett säkert, effektivt och hållbart byggande och ett hållbart användande av mark och naturresurser. I våra uppgifter ingår att förebygga jordskred, ras och stranderosion. SGI arbetar också med att ta fram nya metoder för att sanera förorenade områden. SGI tillhör Klimat- och näringslivsdepartementet och har totalt cirka 100 medarbetare. Huvudkontoret ligger i Linköping och kontor finns i Stockholm, Göteborg och Malmö.
Göta älvdalen är Sveriges mest skredbenägna region och samtidigt det område som bedöms påverkas mest av klimatförändringen framöver. Framtida skred skulle påverka både samhällsviktiga funktioner, riksintressen, Natura2000-områden och inte minst många som bor i Göta älvdalen.
Som geotekniker i sekretariatet för Göta älv får du möjlighet att minska riskerna i denna region du kan göra skillnad, som är till nytta för hela samhället!
Arbetsuppgifter
Det är ett välfinansierat regeringsuppdrag som möjliggör att SGI kan arbeta enligt nya utredningsmetoder med projekt från behovsanalys och fram till färdig åtgärd, optimerad enligt den senaste kunskapen. Här blir du del av en engagerad och prestigelös projektgrupp som drivs av att förbättra förutsättningarna för de som bor och verkar längs Göta älv och samtidigt fördjupa sin kunskap inom geotekniska frågeställningar.

Våra medarbetare är den viktigaste tillgången vi har! För att på bästa sätt utföra samhällsuppdraget, behöver vi kunniga och engagerade människor som arbetar hos oss. Vi behöver också dra nytta av våra olikheter i bakgrund, erfarenhet och kompetens.

Istället för att jobba med små enskilda uppdrag får du möjlighet att jobba med helheten. Vi ser hela Göta älv från Vänersborg till Göteborg som ett stort projekt. Sekretariatet har tillgång till en stor mängd undersökningsresultat. Såväl geotekniska beräkningsverktyg som GIS-program används i hög grad. I vårt arbete får vi en bra överblick av allt underlag med hjälp av GIS. Vi behöver en person med god erfarenhet av att genomföra geotekniska utredningar och att medverka vid åtgärder i lös lera.
Du kommer att leda stabilitetsutredningar samt stötta våra kommuner i deras projektering och under åtgärdsfasen med stöd från kompetenta kollegor.

I arbetet ingår att vara en del av SGI:s beredskapsorganisation som geotekniskt stöd till framför allt räddningstjänsten i händelse av eller vid tidiga indikationer på ras eller skred.
Kvalifikationer
Tjänsten kräver universitets- eller högskoleutbildning: civilingenjör (exempelvis väg och vatten eller samhällsbyggnad) eller liknande utbildning som av arbetsgivaren bedöms vara lämplig för tjänsten. För arbetet krävs goda geotekniska kunskaper, särskilt inom området släntstabilitet. Du bör ha erfarenhet av geotekniskt utredningsarbete samt projektering.

Arbetet innebär många kontakter, både internt och externt, och du behöver därför vara utåtriktad och lyhörd. Vi löser våra uppdrag tillsammans, vilket innebär att du bör tycka om att jobba i grupp/team och att dela med dig av erfarenheter. Du ska kunna uttrycka dig väl i tal och skrift. Du har mycket god datavana och arbetar väl i Microsoft- Officepaket.

Vid urvalet kommer det att läggas stor vikt vid din personliga lämplighet. För att kunna arbeta hos oss ska du dela statens gemensamma värdegrund, http://www.sgi.se/sv/om-sgi/sa-arbetar-vi/vardegrund-och-kompass/

Vi erbjuder
om en statlig myndighet är de flesta av våra anställningsvillkor kopplade till det centrala statliga avtalet men vi har också en del av mer specifika anställningsvillkor. Vi erbjuder dig ett samhällsviktigt uppdrag, spännande och utvecklande arbetsuppgifter med generös syn på kompetensutveckling samt en trevlig arbetsplats med medarbetare i fokus med stort engagemang och arbetsglädje. Vi har generöst med semesterdagar, möjlighet att till viss del arbeta på distans, individuell lön, flexibel arbetstid, ett generöst friskvårdsbidrag, mm.
Vid urvalet kommer det att läggas stor vikt vid din personliga lämplighet.
Fackliga företrädare: Martin Holmén SACO tel. 013-20 18 15, Eva Albin ST tel. 013-20 18 29
Tjänsten är placerad vid Sekretariatet för Göta älv i Göteborg och är en tillsvidareanställning på 100%. Tillträde snarast enligt överenskommelse. Visa mindre

About the position
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.
We now have an exciting opportunity for talented DPD Operators to be based in Gothenburg, Sweden.
Drug Product Delivery (DPD) within Pharmaceutical Technology & Development is the sole internal AstraZeneca department that packs, labels and distributes investigational medicinal products to clinical trial patients. We support launched, pre-launched and products under development within all our therapeutic areas. We work in a fast-paced environment where flexibility and agility enable us to deliver high value to early phase clinical trials.
The DPD Operator role will be a operational role within Distribution one of Drug Product Deliveries three operational skill areas, Material Management, Pack Label and Distribution. We work in an environment where flexibility and agility enable us to deliver high value to early phase clinical trials. To complement our existing team, candidates with the following experiences is of interest:
- Distribution experience from a complex supply chain organization
- Drug Product Knowledge including management of Item/article and lot/batch management to ensure traceability on items/articles in a patient kit including a drug product, packaging material and patient labels from the pharmaceutical industry

Responsibilities
The role holder will contribute to the DPD organization applying their expertise in the complex and regulated GMP environment. The work is focused operational within Distribution. As a DPD operator you will perform and document all the operational work according to written procedures. Be engaged in the development and improvement of internal processes and manage deviations. Be responsible for writing of GMP and SHE procedures within own skill areas and will be responsible for related training and compliance activities. As required maintain defined facilities or equipment according to GMP standards and be proactive to contribute to projects/activities through applying specialist knowledge within appropriate areas.
Distribution responsibilities example
Preparing documentation, receiving and packing of investigational medicinal products to clinical trials. Being the main point of contact when it comes to distribution questions for a number of studies.

Your profile
Essential requirements:
-BSc/MSc in chemistry/pharmacy/engineering or equivalent experience. Preferably 2 years experience within pharmaceutical development
-Understanding the disciplines in Drug Product Delivery, Supply Chain and Pharmaceutical development in order to contribute to an effective Supply Chain organization
-Understanding of principles, applications and management of SHE and GMP in an R&D environment
-Demonstrated ability to work with teams in a culturally diverse, complex and changing environment most internally but to some extent externally
-Good written and verbal English communication and understanding

Soft skills:
As a person, you should have a curious and innovative mindset with problem solving ability, resolving issues with minimal guidance. The perfect candidate should show interest in working operationally to learn and quickly adapt to the new tasks with a willingness to develop within this role

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

About the position
Here at AstraZeneca, we are working towards turning novel state-of-art technologies into effective and safe medicines for severe genetic disease. Do you want to be part of this effort? Welcome to join our exciting journey!

We are looking for a new team member to join our Screening and Automation team in Genome Engineering Department. The role is based in Gothenburg, Sweden, where you will join an international team that develops novel genome engineering technologies and applies these technologies for generation of therapeutic agents. We provide a stimulating environment for innovation and translational application of genome engineering tools. We continually push the boundaries of science to deliver medicines that treat diseases across our main therapy areas.

Responsibilities
You will bring your scientific expertise in molecular biology and innovative thinking to drive genome editing approaches that can lead to therapies. You will be a part of cross-functional project teams with various backgrounds and expertise, where you will contribute to development of gene editing strategies.

Accountabilities will include experimental optimization of genome engineering tools to facilitate efficient gene editing, developing relevant assays, analyzing gene editing outcomes, documenting, interpreting, and communicating results to relevant partners. You will collaborate with others to develop streamlined platforms for high-throughput screening and optimization of genome editing components. This is a very exciting role that will give you exceptional professional and technical development opportunities in this state-of-the art scientific discipline.

We also believe that our new colleague is a person who thinks in a creative way and find innovative approaches to scientific problems. You are enthusiastic and curiosity-driven towards finding answers to scientific questions, coming up with solutions to technical problems and learning new skills. You can work in an independent and goal-oriented way, but you also enjoy team work and have the ability to communicate and collaborate in a global setting with cross-functional groups.

Your profile
• PhD degree?in molecular/cell biology, genetics or relevant areas, or MSc with 2+ years' experience in academia or industry
• Strong molecular biology background and relevant hands-on skills.
• Expertise with mammalian cell culture and cellular assays, such as genetic manipulation
and evaluating genetic & functional outcomes using next generation sequencing, qPCR etc.

Desirable for the role:

• Solid understanding of genome engineering and current technologies.
• Experience with automation and high-throughput application
• Experience with producing and using viral vectors (lenti/AAV) for gene delivery in mammalian cells.

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

About the position
Human Biological Samples (HBS) are fundamental to medical research in the discovery, development and implementation of new treatments and diagnostics. HBS are ethically sensitive materials and the collection, handling and access to HBS are subject to strict regulations, principles and ethical guidelines.

The HBS Compliance Associate Director is responsible for ensuring the compliant use of samples for research.
They are experienced in the review of informed consent and able to ensure samples are used in accordance with patient wishes, protecting our License to Operate.
They will ensure HBS Compliance procedures are followed with regard to HBS specific policies and standards, and can advise stakeholders on use of samples, including decision making on approval of requests for their use in research.

Responsibilities
Review and advise on use of HBS in accordance with patient consent.
Lead the identification and establishment of effective HBS compliance procedures to support review of samples as part of US inventories.
Manage HBS processes to ensure standards are adhered to and compliance requirements are consistently applied for use of HBS in research for samples in the US for the Amnesty project.
Support the business with compliant use of HBS through expert advice and decision making
Ensure risks arising from HBS due diligence activities for US Inventory are identified and recorded.
Maintain the documentation/SOPs associated with HBS due diligence activities for the US Amnesty project.
Monitor the effectiveness of HBS due diligence processes and identify opportunities for improvement.
Perform HBS due diligence reviews for AZ clinical sample use and re-use requests for HBS in the biobank to support delivery of timely and effective decisions.
Act as subject matter expert, reviewing informed consents and making recommendations on HBS use.

Your profile
Required Skills/ Experience/ Education/ Qualifications:
-Bsc. degree
-Experience in pharmaceuticals, a healthcare related industry or academia/hospital environment related to HBS
-Experience in the review of ICFs regarding use of HBS and knowledge of HBS regulations, laws and standards
-Experience of working with multiple stakeholders while maintaining ethical standards and willingness to challenge inappropriate proposals/actions of senior leaders
-Experience in collection and use of HBS as part of ongoing clinical trials is desirable
-Previous experience as a process owner and process improvement is desirable

-Excellent analytical, written and oral communications skills
-Strong collaborative, partnering, and interpersonal skills
-Strong ability to work independently
-Willingness to take decisions
-Excellent knowledge of English, both written and spoken

About the organisation
This is a consultant assignment at AstraZeneca in Gothenburg for 12 months. During this time you will be hired by us at QRIOS.
QRIOS can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives – and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

Human Biological Samples (HBS) are fundamental to medical research in the discovery, development and implementation of new treatments and diagnostics. HBS are ethically sensitive materials and the collection, handling and access to HBS are subject to strict regulations, principles and ethical guidelines.

The AstraZeneca Biobank maintains a data repository with appropriate human subject protection and industry best practices. The Biobank stores HBS, banked or prospectively collected from geographically diverse populations.
We are now looking for you who would like to join our team on a 12-month assignment and play a pivotal role in this exciting period of development!

Responsibilities
The Compliance specialist (CS) role will co-ordinate projects and assist in delivery under the supervision of the Compliance associate Directors and project leads to ensure collation of all information related to HBS. The post holder will be required to work with the biobank to reconcile the HBS inventory against compliance information to allow decision making on inventory.

In addition, you will:
-Collaborate with the internal teams in locating documentation and reviewing consent for requests related to HBS in AZ.
-Assist in knowledge curation to allow decision making on inventory which maybe in AZ, or third parties. Duties may include handling of HBS during the reconciliation and curation process.
-Work with the HBS C&G team and Biobank leads to ensure that learning from HBS related issues are identified and analysed to enable continuous process improvement.
-Electronically manage HBS retrievals including receipt, tracking, review and approval of requests from internal requestors. Confirm requests against the informed consent, raise requests as the need arises.
-Assist with the resolution of issue and queries relating to HBS within the inventory. Maintain records for HBS stored until it meets final disposal and follow destruction process when initiated.

Your profile
• Project management experience and skills is preferable
• Experience with administrative tools
• Experience in pharmaceuticals, a healthcare related industry or academia/hospital environment related to HBS
• Excellent analytical, written and oral communications skills together with excellent English written and verbal communication skills
• Knowledge and understanding of compliance function, health care regulations, laws, and standards (HBS)

-Excellent analytical, written and oral communications skills.
-Proven team working skills
-Ability to work independently
-High ethical standards, trustworthy, operating with absolute discretion

About the organisation
This is a consultant assignment at AstraZeneca in Gothenburg for 12 months. During this time you will be hired by us at QRIOS.
QRIOS can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives – and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

Would you like to utilise your planning and supply chain knowledge to lead clinical supplies for your portfolio of global clinical studies? With constant new products and launches, there has never been a better time to join Global Clinical Supply Chain and shape our future with a significant contribution to life-changing medicines.
We have an exciting opportunity for talented Supply Chain Managers to join our Clinical Study Supply Chain team in Gothenburg, Sweden. This is a key role within our Clinical Manufacturing and Supply teams, and we make sure clinical trial medications are available at the right quality, in the right quantity at the right time for every patient taking part in AstraZeneca’s trials all over the world. Our goal is to never miss a patient.

About the position
In this role you will project manage the design, plan, and set-up of the study supply chain to ensure on time delivery of clinical supplies. You will also lead a cross-functional team enabling continuous dialogue with both internal and external partners on study design requirements and associated changes which may impact the supply chain elements of the study.
To be successful in this role you need to be a fast learner, self-driven and comfortable working in a high pace R&D environment. You need to be a collaborative team player, flexible and have strong communication, planning and problem-solving skills.

Responsibilities
• Project manage the delivery of clinical supplies effectively and consistently, and input to the balance of costs and any risks to supply.
• Ensure effective communication with project teams and key partners across a global network.
• Support risk management of individual studies with proactive mitigation of risks that potentially impact the quality or delivery of supplies.
• Take ownership for Inventory management including any rework and recalls, extensions of shelf life and expiry date management, or stock destruction.
• Manage the Interactive Response Technology (IRT) system to execute demand and supply planning.
• Work within GMP Quality Management Systems ensuring that you actively handle any deviations, complaints and change controls.

Your profile
Essential for the role:
• Experience within a Supply Chain Management environment with a holistic knowledge of end-to-end supply chain activities (minimum 2 years experience desirable)
• Proficient IT skills with an ability to adapt and operate in bespoke multiple systems
• Experience in running projects and in?uencing customer demands
• Experience of demand planning and forecasting and risk identification and management
• Excellent English written and verbal communication skills

Desirable for the role:
• Awareness of GMP (Good Manufacturing Practise) and GCP (Good Clinical Practice)
• Knowledge of clinical development processes relevant to the supply of clinical materials
• Lean knowledge and understanding
• Experienced in handling Quality Events (Deviations, Change Controls, Complaints)
• Knowledge of clinical development processes relevant to the supply of clinical materials
• Working in a leading role within a team

About the organisation
This is a consultant assignment at AstraZeneca in Gothenburg for 1 year. During this time you will be hired by us at QRIOS.
QRIOS can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

Just nu söker jag dig som har intresse av kemikalielagstiftning samt att tolka och utforma säkerhetsdatablad till en kund i Göteborg.

Som Produktsäkerhetsspecialist kommer du att arbeta främst med att klassificera kemiska produkter enligt CLP,
upprätta etikettunderlag, säkerhetsdatablad samt övrig teknisk administration som hör till avdelningen.
En stor del av ditt arbete görs i projektform, där du både driver egna projekt och deltar i projekt i samarbete med produktutvecklarna. Din roll blir att se till att utvecklade produkter följer de lagar och krav som finns för kemiska produkter.

Vem är du?
• Jag söker dig som har kunskap inom kemi, biologi eller toxikologi. Även du som är farmaceut kan vara relevant för jobbet!
• Det är meriterande om du har arbetat med klassificering av kemiska produkter och skapat
• säkerhetsdatablad.
• God datorvana samt goda kunskaper i svenska och engelska är ett krav då arbetet innebär kontakter med kunder och myndigheter i Sverige och övriga Europa.
• Som person är du noggrann och strukturerad samt flexibel och kan prioritera uppdragen efterhand de förändras.


Detta är ett kortare konsultuppdrag hos en global kund inom medtech i Göteborg.
Mer info kommer att delges vid eventuell intervju.
Under uppdragslängden kommer du vara anställd av QRIOS.

Varmt välkommen med din ansökan. Urval sker löpande, ansök därför redan idag genom att klicka på ansök på https://www.qrios.se. Visa mindre

About the position
At AstraZeneca we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.

Inhalation Product Development (IPD) at AstraZeneca is a multinational organization that combines decades of experience in inhalation technology whether it is nebulization, pMDI or DPI. Our vision is to develop and provide to patients best-in-class, innovative and sustainable products to deliver medicine via inhalation.

We’re looking for a talented and motivated Analytical Scientist to join our Analytical Sciences team working with characterization of inhaled molecules within IPD in Gothenburg.

Responsibilities
As an Analytical Scientist you will work independently in the laboratory with analytical testing, documentation and also present your data to the project team.
You will join a highly collaborative team who work with both manual and automated analytical techniques to deliver innovative inhaled medicines to patients.

To be successful in this role you need good skills in written and verbal communication and have a positive problem-solving attitude with delivery focus. You should possess an enthusiasm for laboratory-based work, be flexible and have a collaborative and problem-solving mind-set. This is a lab-based role where you will work collaboratively with colleagues, documenting your experiments carefully to the right quality.

Your profile
Essential for the role:
•Bsc or MSc degree in Analytical Chemistry or other relevant scientific discipline
•Experience from analytical chromatography (UPLC) with relevant detection techniques for small molecules
•Prior experience working as analytical scientist within pharmaceutical industry is desirable
•Experience in aerosol characterization techniques used for inhaled products, such as impactor analysis is desirable
•Experience of working in GMP environment is desirable
•Excellent communication skills and ability to communicate in English both orally and in writing.

Other skills:
o Profound knowledge of the discovery and development phase and awareness of clinical drug development.

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

About the position
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.
We now have the opportunity for one consultant to join our team in the role as a Materials Scientist within the Oral Product Development team at AstraZeneca in Gothenburg. The assignment is to end of Dec 2024 on a temporary basis.

Responsibilities
We are looking for a scientist in Material Science who can provide input in the area of materials characterization during the development of drug products, and can work together with us determining physical properties on materials that we use during the development of, or finalized drug products. The work includes characterization, documentation, and attending and presenting project team meetings. The role is primarily laboratory based.

Your profile
-BSc or MSc typically from pharmaceutics, chemistry or chemical engineering, but also other disciplines with relevant skills.
-Experience from working within the pharmaceutical industry is an advantage.
-Laboratory experience including working with computerized systems.
-Experience of physical characterisation techniques such as laser light scattering (PSD), surface gas adsorption (BET) and powder rheometry (RST/FT4) is desirable.
-Excellent knowledge in written and spoken English is necessary (Swedish is a plus but not mandatory for this position)

As a person, you should be well organized, analytical, flexible and accurate. Good team working skills are also important, together with the ability to operate independently. Good communication skills linked to the ability to work to tight timelines are highly valued.

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

Vi på Soltech Energy Solutions är en samhällsbyggare som driver den gröna omställningen av energisystemet med solenergi som plattform. Detta gör vi nationellt genom storskaliga nätanslutna markbaserade solcellsanläggningar, systemlösningar för energilager och s.k. hybridanläggningar som avlastar elnätet och bidrar till att lösa energi- och effektutmaningen. Vi är ett helägt dotterbolag inom Soltech-koncernen, en av de största spelarna på den svenska solenergimarknaden, och en trygg partner som med över 30 års erfarenhet i branschen vet hur man skapar hållbara, lönsamma och högkvalitativa energilösningar. Vi söker nu en projektör inom elkonstruktion för Business Unit ESS (Energy Storage Solutions), en fristående resultatenhet som arbetar med våra systemlösningar för storskalig energilagring.
Om tjänsten
Som projektör inom elkonstruktion (energilager) är du en drivande kraft i fortsatt utveckling och satsning på energilager och du bidrar till vår gröna vision. Du kommer att stärka upp det tekniska teamet och arbeta med en mängd varierande arbetsuppgifter där några av de viktigaste handlar om att vara en central teknisk kompetens inom det aktuella produktområdet – där du hela tiden håller dig uppdaterad om marknaden och kontinuerligt utvärderar nya produkter och lösningar. Mycket vikt och dagligt arbete ligger i våra projekt, och du fungerar som stöd till övergripande utveckling och materialisering av dessa och säkerställer att våra produkter följer gällande lagar och regler, författningskrav för miljö och hållbarhet osv. Som projektör arbetar du med systematisk utveckling av system- och anläggningsdesign under projektets alla skeden, från införsäljning till driftsatt och överlämnad anläggning. Du ingår i ett välmående och växande team som idag består av 10 medarbetare, och utgår från Stockholm eller Göteborg.
Vem är du?
För att passa i rollen ser vi gärna att du har kompetens sen tidigare av elkonstruktion. Vi tror att du har en teknisk högskoleingenjörs- eller civilingenjörsexamen, t ex som elkraftingenjör med god kunskap om mellanspänning, högspänning, transformatorer, el-nät mm – alternativt har förvärvat dina tekniska kunskaper på annat sätt. Meriterande är också erfarenhet av kommunikation (IT, styr & regler) samt av att ha jobbat i CAD-program. Du är utvecklingsinriktad och en analytisk, självständig och initiativgående lagspelare som värdesätter samarbete och har fokus på problemlösning och långsiktiga mål. Du kommunicerar helst både på svenska och engelska, och har B-körkort. En del resor i Sverige förekommer, men inte i någon större utsträckning.
Om verksamheten
Vi har både ambition och potential att vara ledande på den nordiska solenergimarknaden samt att vara bäst på att utveckla och sälja avancerade produkter och tjänster till många olika typer kunder inom fastighets, bygg- och energibranschen. Soltech Energy Solutions arbetar med större solcellsanläggningar på tak, solcellsparker, batteriparker och hybridparker. Vi vet att det är ett lagarbete och hur viktigt ett gott samarbete är både för att kunna ge våra kunder bästa möjliga lösningar och service, men också för att vi skall ha roligt på jobbet! Soltech Energy Solutions är ett teknikdrivet tjänstemannaföretag bestående av duktiga ingenjörer, projektörer, projektledare, säljare m.m. och finns idag på orterna Stockholm, Jönköping, Göteborg, Falkenberg, Helsingborg och Malmö. För mer information: https://soltechenergysolutions.se/

Urval och intervjuer sker löpande så sök redan idag!
Varmt välkommen med din ansökan!
#LI-DW1 Visa mindre

Vi på Soltech Energy Solutions är en samhällsbyggare som driver den gröna omställningen av energisystemet med solenergi som plattform. Detta gör vi nationellt genom storskaliga nätanslutna markbaserade solcellsanläggningar, systemlösningar för energilager och s.k. hybridanläggningar som avlastar elnätet och bidrar till att lösa energi- och effektutmaningen. Vi är ett helägt dotterbolag inom Soltech-koncernen, en av de största spelarna på den svenska solenergimarknaden, och en trygg partner som med över 30 års erfarenhet i branschen vet hur man skapar hållbara, lönsamma och högkvalitativa energilösningar. Vi söker nu en erfaren projektledare för Business Unit ESS (Energy Storage Solutions), en fristående resultatenhet som arbetar med våra systemlösningar för storskalig energilagring.
Om tjänsten
Du är en drivande kraft i fortsatt utveckling och satsning på energilager och bidrar till vår gröna vision. Som den med det övergripande projektansvaret för EPC ESS-projekt kommer du att leda och fördela arbetet inom tilldelade projekt så att tjänsten levereras med rätt kvalitet, i rätt tid och inom projektbudget för att säkerställa en hög leveranssäkerhet. Du ser till så att projektet har nödvändiga resurser och att medarbetarna har nödvändig utbildning, och du upphandlar och avropar material och tjänster till projekten. Du leder arbetet på siten och är arbetsmiljö-, miljö- och kvalitetsansvarig för projektet under EPC-tiden. Vidare är du bolagets ansikte utåt och därmed dess representant för att bygga långsiktiga och förtroendefulla relationer med kunder och externa partners.?Du överlämnar färdigställt projekt till eftermarknad och service för att säkra dess kontinuerliga förvaltning enligt kontrakt med kund. Du ingår i ett välmående och växande team som idag består av 10 medarbetare, och utgår från Stockholm, Göteborg eller Malmö. Resor i Sverige förekommer, varför du behöver ha ett svenskt B-körkort.
Vem är du?
För att passa i rollen tror vi att du har ett antal års erfarenhet som projektledare, gärna från större entreprenader inom bygg/mark/anläggning/infrastruktur/högspänningsel och liknande. Du har erfarenhet av mark-och entreprenadupphandlingar; kan de olika entreprenadformerna och förstår juridiken kring dessa liksom vikten av att ha en fungerande tidplan och att ha olika risker (som viten) under kontroll. Vi tror också att du har en högskoleingenjörs/civilingenjörsexamen inom bygg- eller maskininteknik, energi eller relaterat område - alternativt har förvärvat dina tekniska kunskaper på annat sätt. Det är bra om du är utbildad och certifierad inom en vedertagen projektmodell såsom PMI, och har du erfarenhet av kravställningsarbete samt goda kunskaper inom entreprenadjuridik och upphandling baserat på ABT06, Ab04, AB-U eller liknande så blir ingen gladare än vi. Du får gärna ha arbetat med projektledning för bygg- och EPC-projekt samt ha erfarenhet av byggpraxis, planering, kontrakthantering, miljö- och säkerhetskrav etc. Du är en god kommunikatör och van att hantera kunder, investerare och beställare, samt brinner för och har god erfarenhet av att knyta och bibehålla stabila kundrelationer över tid. Med stort engagemang och ett systematiskt arbetssätt kombinerat med en förmåga att kritiskt granska uppgifter och på ett analytiskt vis dra slutsatser hur de skall tolkas, är du pådrivande i projekt och mån om att leverera kvalitet inom uppsatta tidsramar. Som person drivs av att åstadkomma förändring, du trivs med ett högt tempo och har ett intresse för hållbarhetsfrågor och förnybar energi. Du är en stabil, strukturerad och uthållig ledare som värdesätter samarbete och har fokus på långsiktiga mål.
Om verksamheten
Vi har både ambition och potential att vara ledande på den nordiska solenergimarknaden samt att vara bäst på att utveckla och sälja avancerade produkter och tjänster till många olika typer kunder inom fastighets, bygg- och energibranschen. Soltech Energy Solutions arbetar med större solcellsanläggningar på tak, solcellsparker, batteriparker och hybridparker. Vi vet att det är ett lagarbete och hur viktigt ett gott samarbete är både för att kunna ge våra kunder bästa möjliga lösningar och service, men också för att vi skall ha roligt på jobbet!
Soltech Energy Solutions är ett teknikdrivet tjänstemannaföretag bestående av duktiga ingenjörer, projektörer, projektledare, säljare m.m. och finns idag på orterna Stockholm, Jönköping, Göteborg, Falkenberg, Helsingborg och Malmö. För mer information: https://soltechenergysolutions.se/

Urval och intervjuer sker löpande så sök redan idag!
Varmt välkommen med din ansökan!
#LI-DW1 Visa mindre

Vi på Soltech Energy Solutions är en samhällsbyggare som driver den gröna omställningen av energisystemet med solenergi som plattform. Detta gör vi nationellt genom storskaliga nätanslutna markbaserade solcellsanläggningar, systemlösningar för energilager och s.k. hybridanläggningar som avlastar elnätet och bidrar till att lösa energi- och effektutmaningen. Vi är ett helägt dotterbolag inom Soltech-koncernen, en av de största spelarna på den svenska solenergimarknaden, och en trygg partner som med över 30 års erfarenhet i branschen vet hur man skapar hållbara, lönsamma och högkvalitativa energilösningar. Vi söker nu en erfaren entreprenadchef för Business Unit ESS (Energy Storage Solutions), en fristående resultatenhet som arbetar med våra systemlösningar för storskalig energilagring.
Om tjänsten
Du är en drivande kraft i fortsatt utveckling och satsning på energilager och bidrar till vår gröna vision. Som den med det övergripande entreprenadsansvaret för EPC ESS-projekt kommer du att leda och samordna arbetet för en handfull projektledare, vilket innebär ett helhetsansvar för projektportföljen inkl. tidplan, ekonomi, kvalitet och liknande. Som entreprenadchef ansvarar du också för arbetsmiljön och fungerar som ett operativt stöd för dina projektledare. I praktiken innebär det senare att du stödjer dem med löpande råd och rekommendationer avseende kommersiella och kontraktsmässiga frågor som påverkar projektverksamheten, samt säkerställer kontinuerlig förbättring. Du ser till så att dina medarbetare har den kompetens som behövs och får den utbildning som krävs för att utföra ett högkvalitativt arbete. Därtill driver du själv några EPC-projekt per år, liksom underhåller goda relationer med kunder och serviceleverantörer. Det faller på din lott att säkerställa att de upphandlade underleverantörerna uppfyller SES krav och utför sina uppdrag därefter. Du ingår i ett välmående och växande team som idag består av 10 medarbetare, och utgår från Stockholm, Göteborg, Jönköping eller Malmö. Resor i Sverige förekommer, varför du behöver ha ett svenskt B-körkort.
Vem är du?
För att passa i rollen tror vi att du har minst 3 års erfarenhet av ledarskap liksom en examen inom någon ingenjörsvetenskap såsom byggteknik, maskinteknik, energi eller ett relaterat område - alternativt har förvärvat dina tekniska kunskaper på annat sätt. Vi ser gärna att du har god erfarenhet av projektledning för bygg- och EPC-projekt, liksom av att leda en organisation och projektportfölj med avseende på mål, budget, prestanda och överensstämmelse. Kunskap om svensk byggnadslagstiftning såsom ABT06, ABU etc är ett stort plus, precis som erfarenhet av byggpraxis, planering, kontrakthantering, miljö- och säkerhetskrav och liknande är det. Du har ett stort driv och ett systematiskt arbetssätt, samt en stark vilja att leverera kvalitet inom angivna tidsramar. Vi blir mycket glada om du besitter utmärkta skriftliga och muntliga kommunikationsfärdigheter (svenska och engelska) samt har erfarenhet av hybrid- och flerfunktionella kontorsledningsmiljöer. Du har erfarenhet och vana av kundkontakter och av att bygga kundrelationer, samt en stark förmåga att kritiskt granska och analysera data. Som person drivs av att åstadkomma förändring, du trivs med ett högt tempo och har ett intresse för hållbarhetsfrågor och förnybar energi. Du är en stabil, strukturerad och uthållig ledare som värdesätter samarbete och har fokus på långsiktiga mål.
Om verksamheten
Vi har både ambition och potential att vara ledande på den nordiska solenergimarknaden samt att vara bäst på att utveckla och sälja avancerade produkter och tjänster till många olika typer kunder inom fastighets, bygg- och energibranschen. Soltech Energy Solutions arbetar med större solcellsanläggningar på tak, solcellsparker, batteriparker och hybridparker. Vi vet att det är ett lagarbete och hur viktigt ett gott samarbete är både för att kunna ge våra kunder bästa möjliga lösningar och service, men också för att vi skall ha roligt på jobbet! Soltech Energy Solutions är ett teknikdrivet tjänstemannaföretag bestående av duktiga ingenjörer, projektörer, projektledare, säljare m.m. och finns idag på orterna Stockholm, Jönköping, Göteborg, Falkenberg, Helsingborg och Malmö. För mer information: https://soltechenergysolutions.se/

Urval och intervjuer sker löpande så sök redan idag!
Varmt välkommen med din ansökan!
#LI-DW1 Visa mindre

About the position
At AstraZeneca, we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big, and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.

We continually push the boundaries of science to deliver medicines that treat diseases across our main therapy areas. Through our integration with Alexion, this now includes expanding the limits of scientific research to better understand rare diseases and to discover new life-changing treatments for them.

Pharmaceutical Sciences is a department within AstraZeneca Biopharmaceutical R&D. The Pharmaceutical Sciences’ mission is to transform molecules into investigational medicines, meeting the unmet needs of future patients. Advanced Drug Delivery is a department in Pharmaceutical Sciences. Our portfolio of projects spans traditional small molecules, proteins, oligonucleotides to RNA based therapeutics across AstraZeneca’s therapy areas and our mission is to transform diverse modalities into investigational medicines.
We are now recruiting a hardworking and motivated Scientist to join our GMP Analytics team within the Advanced Drug Delivery (ADD) function in Gothenburg, Sweden. The role sits within the ADD group at our vibrant R&D site in Gothenburg, Sweden. With more than 2 800 employees from over 70 different countries, our vibrant Gothenburg site is a truly inspiring place to work.

Responsibilities
As a scientist, you will be part of the development of analytical methods, stability assessments as well as exploratory scientific initiatives. Additionally, you will perform analytical work to support the clinical phase development, such as validation of analytical methods, release analysis and stability studies. Part of the work is performed according to Good Manufacturing Practice (GMP).

You will be a member of different drug development project teams, representing your skill and scientific area. You will work in close collaboration with formulation scientists, analytical chemists as well as biopharmaceutics experts at AstraZeneca in Sweden, UK and US. Profound knowledge of the discovery and development phase as well as awareness of clinical drug development are central for being successful in this role.

We are looking for you, who together with your team will make a difference for patients' lives every day. This through your ability to independently lead and achieve set goals within budget, time and to the right quality

Your profile
• MSc in a relevant scientific field (such as Analytical Chemistry, Biochemistry or Biotechnology)
• In-depth knowledge of analytical methodologies such as chromatography, mass spectrometry and other biophysical/chemical characterization techniques
• Understanding of principles and applications of GMP
• An interest in exploratory analytical work related to complex molecules, delivery systems and new technologies
• Ability to communicate in English both orally and in writing
• Thorough understanding of principles, applications and management of Safety Health and Environment (SHE)

About the organisation
This is a consulting assignement at AstraZeneca in Gothenburg for one year starting in February 2024. During this time you will be hired by QRIOS.
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

Vi på Soltech Energy Solutions är en samhällsbyggare som driver den gröna omställningen av energisystemet med solenergi som plattform. Detta gör vi nationellt genom storskaliga nätanslutna mark- och takbaserade solcellsanläggningar, systemlösningar för energilager och s.k. hybridanläggningar som avlastar elnätet och bidrar till att lösa energi- och effektutmaningen. Vi är ett helägt dotterbolag inom Soltech-koncernen, en av de största spelarna på den svenska solenergimarknaden och en trygg partner som med över 30 års erfarenhet i branschen vet hur man skapar hållbara, lönsamma och högkvalitativa energilösningar. Vi söker nu 1-2 tekniska projektutvecklare primärt i Stockholm (men Göteborg, Falkenberg el. Jönköping är också möjligt) för Business Unit C&I (Commercial & Industrial), en fristående resultatenhet som arbetar med större solenergianläggningar inom fastighetens säkring, dvs både på tak och mark. Soltech är en av få aktörer på den svenska marknaden som har både kunskap, kapacitet och erfarenhet av byggnation av solcellsanläggningar i Megawatt storlek på tak.
Om tjänsten
Som teknisk projektutvecklare är du en drivande kraft i fortsatt utveckling och satsning på smarta energilösningar i form av solcellsanläggningar/energilager/laddinfrastruktur och du bidrar till vår gröna vision. Du kommer att stärka upp det tekniska teamet och arbeta med en mängd varierande arbetsuppgifter där några av de viktigaste handlar om att vara en central teknisk kompetens inom det aktuella produktområdet – där du hela tiden håller dig uppdaterad om marknaden och kontinuerligt utvärderar nya produkter och lösningar. Mycket vikt och dagligt arbete ligger i våra projekt, och du fungerar som stöd till övergripande utveckling och materialisering av dessa och säkerställer att våra produkter följer gällande lagar och regler, författningskrav för miljö och hållbarhet osv. Som teknisk projektutvecklare ansvarar du för att ta fram och ständigt arbeta med systematisk utveckling av systemdesign & anläggningsdesign med tillhörande energiflödeskalkyler, optimering gentemot LCOE/LCOS samt ritningspaket för projektet och under projektets alla skeden, från införsäljning till driftsatt och överlämnad anläggning. Du ingår i ett välmående och växande team som idag består av 25 medarbetare, och utgår från Stockholm, Jönköping, Göteborg eller Falkenberg.
Vem är du?
För att passa i rollen ser vi gärna att du har kompetens sedan tidigare inom projektering av solcellanläggningar och batterier/BESS. Det är meriterande om du även har erfarenhet av elkonstruktion. Vi tror att du har en teknisk högskoleingenjörs- eller civilingenjörsexamen – alternativt har förvärvat dina tekniska kunskaper på annat sätt. Kunskaper inom digitala verktyg för systemdesign och energiflödesanalys är meriterande (såsom PVSYST eller PVSOL) liksom erfarenhet av att ha jobbat i Auto-CAD. Du är utvecklingsinriktad och en analytisk, självständig och initiativgående lagspelare som värdesätter samarbete och har fokus på problemlösning och långsiktiga mål. Du kommunicerar helst på både svenska och engelska, och har B-körkort. En del resor i Sverige förekommer, men inte i någon större utsträckning.
Om verksamheten
Vi har både ambition och potential att vara ledande på den nordiska solenergimarknaden samt att vara bäst på att utveckla och sälja avancerade produkter och tjänster till många olika typer kunder inom fastighets, bygg- och energibranschen. Soltech Energy Solutions arbetar med större solcellsanläggningar på tak, solcellsparker, batteriparker och hybridparker. Vi vet att det är ett lagarbete och hur viktigt ett gott samarbete är både för att kunna ge våra kunder bästa möjliga lösningar och service, men också för att vi skall ha roligt på jobbet! Soltech Energy Solutions är ett teknikdrivet tjänstemannaföretag bestående av duktiga ingenjörer, projektörer, projektledare, säljare m.m. och finns idag på orterna Stockholm, Jönköping, Göteborg, Falkenberg, Helsingborg och Malmö.
För mer information: https://soltechenergysolutions.se/

Urval och intervjuer sker löpande så sök redan idag!
Varmt välkommen med din ansökan!
#LI-DW1 Visa mindre

Would you like to utilise your planning and supply chain knowledge to lead clinical supplies for your portfolio of global clinical studies? With constant new products and launches, there has never been a better time to join Global Clinical Supply Chain and shape our future with a significant contribution to life-changing medicines.

We have an exciting opportunity for talented Supply Chain Managers to join our Clinical Study Supply Chain team in Gothenburg, Sweden. This is a key role within our Clinical Manufacturing and Supply teams, and we make sure clinical trial medications are available at the right quality, in the right quantity at the right time for every patient taking part in AstraZeneca’s trials all over the world. Our goal is to never miss a patient.

In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that help millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines – from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.

About the position
In this role you will project manage the design, plan, and set-up of the study supply chain to ensure on time delivery of clinical supplies. You will also lead a cross-functional team enabling continuous dialogue with both internal and external partners on study design requirements and associated changes which may impact the supply chain elements of the study.

To be successful in this role you need to be a fast learner, self-driven and comfortable working in a high pace R&D environment. You need to be a collaborative team player, flexible and have strong communication, planning and problem-solving skills.

Responsibilities
Your main responsibilities will include:
• Project manage the delivery of clinical supplies effectively and consistently, and input to the balance of costs and any risks to supply.
• Ensure effective communication with project teams and key partners across a global network.
• Support risk management of individual studies with proactive mitigation of risks that potentially impact the quality or delivery of supplies.
• Take ownership for Inventory management including any rework and recalls, extensions of shelf life and expiry date management, or stock destruction.
• Manage the Interactive Response Technology (IRT) system to execute demand and supply planning.
• Work within GMP Quality Management Systems ensuring that you actively handle any deviations, complaints and change controls.

Your profile
Essential for the role:

• Bachelor’s Degree in Supply Chain, business or scientific subject area – equivalent experience within Supply Chain will be considered
• Experience within a Supply Chain Management environment with a holistic knowledge of end-to-end supply chain activities (minimum 2 years experience desirable)
• Proficient IT skills with an ability to adapt and operate in bespoke multiple systems
• Experience in running projects and in?uencing customer demands
• Experience of demand planning and forecasting and risk identification and management
• Excellent English written and verbal communication skills

Desirable for the role:

• Awareness of GMP (Good Manufacturing Practise) and GCP (Good Clinical Practice)
• Knowledge of clinical development processes relevant to the supply of clinical materials
• Lean knowledge and understanding
• Experienced in handling Quality Events (Deviations, Change Controls, Complaints)
• Knowledge of clinical development processes relevant to the supply of clinical materials
• Working in a leading role within a team

About the organisation
This is a consultant assignement at AstraZeneca in Göteborg for 1 year. During this time you will be hired by QRIOS Life Science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

About the position
The Diagnostic Project Management group within Precision Medicine, Project, Portfolio & Alliances is accountable for providing project and portfolio management to ensure successful delivery of diagnostic projects from initiation of development to regulatory approval, across all therapy areas, and to further optimise the delivery of precision medicines by defining and fostering best practices. Furthermore, this group is responsible for driving continuous improvement processes, for providing accurate Precision Medicine portfolio information for decision making and business reporting, and for capacity and resource management.

The Assoc Director Diagnostic Project Management will work across several cross-functional diagnostic project/ programme teams to provide hands on project management expertise to deliver projects within agreed time, budget and quality. The role depends on close collaboration with Project Managers and project teams to ensure strategic alignment, and with Information Managers, who are responsible for inputting project information into AZ’s enterprise planning tool (PLANIT).

Responsibilities
• Manages multiple complex projects to deliver to time, cost and quality
o Creates and manages project plans to supervise and drive delivery of major milestones
o Manages project costs aligned to investment decisions, and FTE resources aligned to project needs/ forecast demand
o Creates and manages project risk logs, and drives mitigating actions with diagnostic project teams
o Creates progress reports to track delivery to time, cost and quality
• Coaches, and works with, Diagnostic Information Managers to ensure accuracy of project/ portfolio information within AZ’s enterprise planning tool (PLANIT)
• Drives process simplification and standardisation across Precision Medicine to maximise efficiencies and establish best practice
• Meeting planning and facilitation
• Plans and facilitates Diagnostic Project Team meetings, ensuring accurate actions are captured, circulated and followed up on.
• Plans and facilitates Precision Medicine project review meetings, attended by Precision Medicine leaders, diagnostic project team members and key R&D stakeholders
• Deputises for the Diagnostic Project Manager at programme level, as necessary

Your profile
Requirements
• BA/BSc in relevant subject (or equivalent experience)
• Significant experience within a scientific project management environment
• Expert understanding of Project Management techniques, tools and principles
• Strong organisation and forward-planning skills, with attention to detail
• Experience of global team-working and effectively communicating with key stakeholders
• A professional, enthusiastic and proactive approach, with the ability to independently manage a diverse and fast paced workload
• Experience of using Microsoft Office/ Outlook, project planning tools and web-based programmes
• Prior experience in managing and reporting of project information

Preferred Experience
• Professional project management qualification (e.g. PMP)
• High-level understanding and curiosity about Precision Medicine
• Experience of using PLANIT to accurately forecast resource and maintain milestones

About the organisation
This is a consultant assignment at AstraZeneca in Göteborg from January - November 2024. During this time you will be hired by us at QRIOS.

QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

QRIOS Life Science & Engineering är i behov av kompetenta medarbetare för flera spännande konsultuppdrag. Vi välkomnar sökande med minst tre års erfarenhet inom områdena Mechanics & Cabling samt Electronics.
Mechanics & Cabling
Vi letar efter kandidater med erfarenhet inom följande områden:

Miljökrav -Maritima, markbaserade och luftburna domäner


Kunskap inom mikrovågsteknik


Expertis inom kraftelektronik


Hantering av äldre teknik på grund av långa produktlivscykler


Erfarenhet av Chrome 6


Användning av Creo (Mech Solid modellering + cabling)


Färdigheter inom Visio (cabling)


Användning av PDM System (IFS)


Electronics
Vi söker individer med erfarenhet inom följande områden:

RF/Mikrovågsdesign


Digital design


PCB-design



Dessa tjänster är konsultuppdrag hos vår kund i Göteborg. Under denna tid kommer du att vara anställd av QRIOS Life Science & Engineering.
QRIOS anställer nyfikna experter inom IT, Life Science och Engineering. Vi vill fortsätta att attrahera de bästa medarbetarna för att kunna stödja våra partners med de viktiga kompetenser de behöver. Vi är ett rekryterings- och konsultföretag som starkt inspireras av dem som aldrig slutar söka efter nya lösningar. Som vi säger, QRIOS MINDS GO FURTHER.

#LI-HF3 Visa mindre

About the position
At AstraZeneca, we unlock the power of What Science Can Do. Empowered to explore, every day we work towards our ultimate aim - treating, preventing, modifying and even curing complex diseases. Be part of the team where you are empowered to follow the science!

Pharmaceutical Sciences (PharmSci) is responsible for the design and development of synthetic routes, preclinical and phase I/II formulations, encompassing both small molecules and new modalities such as mRNA and oligonucleotides, across the whole range of AstraZeneca’s therapeutic areas.

The manufacturing unit within Early Product Development and Manufacture (EPDM) in Gothenburg is accountable for manufacture of a large and variable portfolio of early investigational medicinal products (oral solution/suspension, parenteral solutions, capsules, tablets and inhalers), mainly for Phases I and II. We supply drug product to AZ clinical studies globally and are a vital part to enable early phase clinical trials, delivering a critical step on the path from idea to patient. In short, we are the first in line to manufacture what could improve the lives of patients around the globe.

We are now looking for a Scientist starting as soon as possible with the location Gothenburg, Sweden.

Responsibilities
Within the EPDM manufacturing unit, in the GMP (Good Manufacturing Practice) arena, you will make an important contribution in delivering clinical results in the development of new medicines. This role revolves around the manufacturing of drug product where all activities below will have a significant impact on the speed, quality and cost of the AZ development portfolio.
We expect the successful candidate to:
• Assume responsibilities toward timely manufacture of various drug products in line with the plans agreed within EPDM and surrounding stakeholders.
• Work with practical hands-on processes in our GMP facilities following manufacturing batch records and perform transactions in material management systems.
• Monitor, secure and follow up on other regulatory requirements according to GMP through associated IT-systems.
• Rapidly develop strong competence within relevant process technologies and build credibility and ability to drive and secure product establishment, scale-up and clinical manufactures.
• Support documentation activities, e.g. by authoring manufacturing batch records, taking part in deviation investigations, authoring SOPs, and other guidance documents, change control processes etc.
• Assess records and report manufacturing and validation data accurately according to GMP.
• Ensure that SHE (Safety Health and Environment) and GMP standards are upheld and ensure AZ Policies and Standards are understood and followed.
• Be entrepreneurial and drive initiatives to further improve flexibility and productivity, resulting in shorter lead times or increased value for our customers and patients.

Your profile
In joining EPDM and PharmSci, you will be part of an amazing group of skilled and driven colleagues who truly embrace team spirit, who you will exchange knowledge and collaborate with on many levels in various contexts. This provides excellent opportunities for your professional development, and possibilities to take on further accountabilities in line with your personal growth.
Do you have the essential qualifications for these roles?
We are looking for a Scientist with excellent collaboration, communication, and planning skills with a strong sense of responsibility, team work and delivery focus.
Strong verbal and documentation skills in English is a requirement. We expect you to have a keen interest to learn and operate complex manufacturing equipment and develop your expertise in pharmaceutical process technology. Experience from pharmaceutical development or working in a manufacturing or supply chain organisation and knowledge of cGMP is a merit for this role.

To be considered for this role, you need to have a MSc in pharmacy/engineering and/or extensive GMP-manufacturing experience from the pharmaceutical industry.

About the organisation
This position is a consultant assignment at AstraZeneca starting in January 2024 and ends in July 2024. During this time you will be employed by QRIOS.

QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER Visa mindre

About the position
We’re looking for a talented and motivated analytical chemist to join our Separation Science Laboratory team within the Pharmaceutical Science function at AstraZeneca in Gothenburg.
The vision for Pharmaceutical Sciences is to deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes and manufacturing of Active Pharmaceutical Ingredients (API). Our portfolio of projects spans traditional small molecules to nucleotide-based therapies and nanomedicines across AstraZeneca’s therapy areas.

Responsibilities
You will join a highly competent team and collaboratively drive the delivery of pure compounds to our early portfolio. With a background in separation science, you’ll demonstrate expertise applied to the purification and characterization of synthetic Peptides, Oligonucleotides and molecular conjugates thereof.
This is a laboratory-based role where you will be accountable for providing separation science expertise and facilitate the delivery of different new modalities with right quality to portfolio projects across our therapy areas within AstraZeneca. The team is working in close collaboration with scientists in other functions with the goal to develop the therapeutics of the future. We believe that our new colleague has a problem-solving mindset and can find innovative approaches to complex scientific questions. You work well independently, but you also enjoy teamwork and collaboration and can communicate well across functional boundaries.

You are expected to:

• Be laboratory based and work collaboratively with colleagues
• Run and maintain chromatographic equipment
• Effectively operate with scientists from other functions in a highly cross-disciplinary environment

Your profile
Essential requirements
• Scientific knowledge within analytical chemistry
• Technical skills and experience to use and maintain chromatographic equipment
• Excellent problem-solving skills
• Excellent English, both spoken and written
• Work collaboratively, prioritize your own work and act decisively

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.

QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER Visa mindre

For our client who is a global leading hygiene and health company I am searching for a talent with IT and engineering skills for an assigment focusing on test.
This is a small team in IT Services organization working with connected hardware, supporting both increased innovation and productivity through bundled expertise and delivery support.

Responsibilities
What you will do
Some of your key tasks will be:
• Set up the test environment
• Ensure test cases are available and documented (with support from stakeholders)
• Perform tests on physical products (connected hardware) and document the outcome
• Support engineers with root cause analysis
• Be available for other assignments

Your profile
Who you are
• Recently graduated from gymnasium (4-årig teknisk), college or university
• IT and engineering knowledge/interest
• Curious and willing to learn
• Structured
• Problem-solving skills and ability to work independently and as part of a team
• Be able to document in english

Additional information
• Start date as soon as possible, end-date June 30, 2024 but can be prolonged based on the needs
• Preferably full-time, 80% could also work

About the organisation
This is a consultant assignment until end of June 2024. During this time you will be hired by us at QRIOS. Visa mindre

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because an opportunity no matter how small can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential.
The AstraZeneca CVRM Research group in Gothenburg is seeking to recruit a high calibre scientist to enable progression of a growing drug project portfolio. Highly motivated scientists are encouraged to apply for the opportunity to join our team of professionals who are passionate about advancing science, to discover and develop novel therapeutics that will benefit patients.

About the position
You will play an active role in implementing and executing scientific research within a CVRM Metabolism project, enabling studies aimed at exploring disease modifying mechanisms linked to pharmacological inhibition of the biological target of interest. This is a "hands-on," laboratory based scientific and technical role in our in vitro metabolism team supporting projects from target validation to lead optimisation phases.

Responsibilities
Responsibilities
• Responsibility for design, execution and analysis of in vitro and ex vivo assays.
• Communicate results, conclusions and recommendations to colleagues, line manager and the project team.
• Record experiments in lab books and databases according to AstraZeneca policy.
• Play a leading role in assay development and optimisation of in vitro assays.
• You would report to an expert member of staff and would be encouraged to be able to plan your daily work within direction set by your supervisor.

You will:
• Be asked to provide interpretation of assay results.
• Work within a line and/or matrix/project team.
• Demonstrates scientific rigor in assessing own data and that of others.
• Be a "hands-on" expert with in vitro models and methodologies.

Your profile
Degree in one of the Life Sciences disciplines and equivalent post-graduate or industry experience.

Essential
• Be a "hands-on" expert with in vitro models and methodologies.
• Ability to develop new methods, technologies, and processes
• Enthusiasm for laboratory work, scientific curiosity.
• Experience in running in vitro biochemical and cellular assays to provide potency and activity readouts, including use of primary and recombinant cell lines.
• Significant cell culture experience.
• Experience with disease relevant cell types such as primary hepatocytes or hepatocyte-like cell lines in 2D cultures.
• Experience with ex vivo analysis of blood/tissue samples (including qPCR for gene expression, Western blots, and ELISA).
• Experience in data analysis and interpretation and enthusiasm for problem solving for scientifically challenging work.
• Demonstrable ability to work within a line and/or matrix/ cross-functional project team.
• Strong interest in providing materials and data for scientifically challenging work.
• Strong organizational, time management and communication skills.
• Strong, demonstrable analytical ability.
• Good oral and written communications skills.

Desirable
• Background in metabolic disease research areas.
• Experience with 3D spheroid models and expertise to establish and evaluate models of liver disease in the context of steatosis and fibrosis.
• Knowledge and experience with automation and robotic methods for increasing throughput and medium to high density microtitre plate technologies.
• An understanding of biological sciences, familiarity with the drug discovery process.
• Experience working in pharmaceutical or biotech environment.

Behavioral competencies
• Hard working, organized, balanced and meticulous with an ability to work well under pressure.
• Adaptable and a team player with a conscientious attitude and enthusiasm.
• Desire to learn and build on the role.

About the organisation
This position is a consultant assignment for one year at AstraZeneca in Göteborg. During this time you will be employed by QRIOS.

QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER. Visa mindre

Do you have expertise in, and have a passion for Procurement? Would you like to be part of a high performing R&D procurement team passionate about delivering real value to AstraZeneca’s R&D units to ensure we optimally deliver our strong and ambition R&D pipeline? Are you ready to be part of a company that has set bold sustainability targets, is data driven, follows the science and turns ideas into life changing medicines? If so, then AstraZeneca might be the one for you!

About the position
This is an exciting opportunity to partner with AstraZeneca’s R&D units to drive their research efforts forward to develop medicines for patients. You will have accountability for a global spend category for AstraZeneca (may be single or multiple SET areas). Partnering with stakeholders you will develop long term strategic plans for the entire spend area within AstraZeneca or Region. Managing customer and supplier relationships to ensure that Category Strategies are highly aligned to current and future Business needs and that the supply base can support these strategies. Overseeing implementation of the category plan to ensure that the underpinning process improvement and procurement activities deliver the expected business value in accordance with the strategic plans.

Responsibilities
• Oversees implementation of category plans to ensure that the underpinning process improvement and procurement activities deliver the encouraged business value in accordance with the strategic plans
• Supports Director/ Associate Director in the development of long-term strategic plans for agreed scope of spend area
• Supports the Director/ Associate Director in strategic relationship management (customer and supplier) - to ensure that Market & Category Strategies are highly aligned to current and future Business need and that the supply base can support these strategies.
• Works with relevant Director/ Associate Director(s) to ensure a fully integrated and customer-aligned AZ-wide category plan
• Coordinates the introduction of new and modified products and services with appropriate departments
• Advises on contracts and agreements for the supply of complex products and services with new and existing suppliers
• Develops, evaluates, or manages internal and external relationships with suppliers and other cross-functional teams

Your profile
Essential experience & skills
• Degree level or equivalent qualifications
• Project management, change management and people management skills
• Ideally a working knowledge of the pharmaceutical or healthcare industry
• Strong track record of technical expertise in Procurement, creating value for the organisation through developing industry leading category strategies
• Good communication skills, an ability to influence others and someone who has awareness of how to work across cultures
• Comfort with risk and ambiguous situations
• Curious mindset and a desire to challenge yourself to want to continuously learn and develop

About the organisation
This is a consultant assignment at AstraZeneca in Göteborg until 2024-10-01. During this time you will be hired by QRIOS.
QRIOS can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

About the position
Do you have experience in clinical study management and would like a role where your expertise, as well as your leadership skills, will be highly appreciated? Are you team oriented and do you, as we do, put patients first in your work to make a difference? Then AstraZeneca might be the right place for you to contribute and thrive.
We are recruiting for a Global Study Associate Director (GSAD) who will join our Study Management Cardiovascular Renal Metabolic Diseases (CVRM) team – which forms part of BioPharmaceuticals Clinical Operations . The position will be based in our vibrant R&D sites in Gothenburg, Sweden.

Study Management CVRM, are accountable for delivering high quality, cost efficient clinical studies (phase 1 to phase 3) that support drug development within Cardiovascular Renal Metabolism (CVRM).

Responsibilities
• Lead, provide guidance and delegate appropriately to a cross-functional study team or oversee outsourced delivery activities to ensure the clinical study progresses as planned, driving achievement of milestones according to timelines, budget and quality standards. May hold accountability and/or oversight of several studies.
• Lead and facilitate communication across all functions, including external partners and service providers. Lead and conduct investigator meetings and other study related meetings.
• Provide input into and hold accountability for the development of essential study level documents (i.e., Clinical Study Protocol (CSP) through to Clinical Study Report (CSR)) in accordance with relevant AZ SOPs.
• Ensure all external service providers (i.e., Contract Research Organizations (CROs), central laboratories, IXRS, ePRO, etc.) engaged at the study level are performing to contracted goals and timelines/budget and that adequate oversight is documented and any issues are escalated appropriately. May participate in vendor selection activities.
• Develop and maintain relevant study plans including required input into study level quality and risk management planning (e.g., risk-based quality management, proactive risk and contingency plans, etc.) ensuring that the risk response strategies and issue escalation pathways are clear to the entire study team
• Accountable for ensuring that information in all systems utilized at a study-level are current and accurate.
• Oversee study level performance against agreed upon plans, milestones and key performance indicators (KPIs, quality and operational) by using company tracking systems and project timelines and communicate any risks to timelines and/or quality with proposed mitigations
• Identify and report quality issues that have occurred within the study in accordance with relevant AZ SOP and collaborate with all functions as necessary to overcome barriers and achieve milestones; proactively communicate findings and corrective action plans (CAPAs) to relevant stakeholders
• Oversee Trial Master File (TMF) completion in accordance with relevant AZ SOPs, including ensuring the TMF plan and Expected Document List (EDL) are in place and that QC activities are performed on an ongoing basis to ensure TMF completeness at all times
• Ensure timely compliance with company-wide governance controls (e.g., Delegation of Authority, Sunshine Act, financial system attestations, Clinical Trial Transparency)
• The GSAD is responsible for study budget re-forecasting following initial budget estimate provided by the CPT and accountable for study budget management through the study lifecycle and for providing budget progress reports to the CPT including any financial risks and mitigation plans (as part of the ongoing study change control process)
• Ensure studies are inspection-ready at all times, according to ICH-GCP and AZ SOP and relevant policies/guidelines; GSAD is the primary Study Management point-of-contact in the event of an audit or inspection

Your profile
Essential Requirements:
• University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research
• 5 years of relevant clinical experience in the pharmaceutical industry, including 2 years’ project management experience, or equivalent combination of education, training and experience
• Extensive knowledge of ICH-GCP, clinical research regulatory requirements and demonstrated abilities in clinical study management processes and clinical/drug development
• Demonstrated solid project management skills and knowledge of relevant tools
• Strong, demonstrated abilities/skills in team leadership
• Strong abilities in establishing and maintaining effective working relationships with internal and external co-workers and stakeholders, along with strong conflict management skills
• Excellent communication and interpersonal skills
• Strong strategic and critical thinking abilities
• Strong organizational and problem-solving skills
• Ability to manage competing priorities

Desirable Requirements:
• Advanced degree, Masters level education (or higher)
• Project management certification
• Proven project management experience on a global level
• Experience in all phases of a clinical study lifecycle

About the organisation
This is a consultant assignment at AstraZeneca in Goöteborg until 2024-09-30. During this time you will be hired by QRIOS.
QRIOS can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

Statens geotekniska institut (SGI) är en expertmyndighet som arbetar för ett säkert, effektivt och hållbart byggande och ett hållbart användande av mark och naturresurser. I våra uppgifter ingår att förebygga jordskred, ras och stranderosion. SGI arbetar också med att ta fram nya metoder för att sanera förorenade områden. SGI tillhör Klimat- och näringslivsdepartementet och har totalt cirka 100 medarbetare. Huvudkontoret ligger i Linköping och kontor finns i Stockholm, Göteborg och Malmö.

Vi erbjuder dig
Som en statlig myndighet är de flesta av våra anställningsvillkor kopplade till det centrala statliga avtalet men vi har också en del mer specifika anställningsvillkor. Vi erbjuder dig ett samhällsviktigt uppdrag, spännande och utvecklande arbetsuppgifter med generös syn på kompetensutveckling samt en trevlig arbetsplats med medarbetare med stort engagemang och arbetsglädje i fokus. Vi har generöst med semesterdagar, möjlighet att till viss del arbeta på distans, individuell lön, flexibel arbetstid och ett generöst friskvårdsbidrag.
Arbetsuppgifter
Hos oss erbjuds du intressanta och varierande arbetsuppgifter som har stor betydelse för framtidens samhällsplanering. Vi arbetar med såväl forskning som rådgivning och kunskapsförmedling.

I ditt arbete med stranderosionsfrågor kommer arbetsuppgifterna i stor utsträckning att vara kopplade till att genomföra aktiviteter i vår handlingsplan för hållbart markbyggande i ett föränderligt klimat. En viktig del av ditt arbete kommer att vara att öka och utveckla förståelsen kring betydelsen av erosion i vattendrag för långsiktig påverkan på släntstabilitet och markanvändning. Det kan t.ex. handla om att utveckla förståelse och metoder för hur erosionstakten i vattendrag på olika sätt kan bedömas i dagens och framtidens klimat. Det kan också handla om att utveckla naturanpassade erosionsskydd och en förståelse för hur hydrologi, strömning och sedimentflöden samt olika typer av erosionsskydd samverkar med faktorer som morfologi och ekosystem på land och i vatten.

I ditt arbete med erosion i vattendrag på SGI kommer du tillsammans med kollegor få möjlighet att arbeta med frågor inom flera av följande områden:
• Utvärdera och vid behov förbättra metodik för att bedöma erosion och sedimentdynamik i vattendrag.
• Utveckla kunskapen om dimensionering och utformning av naturanpassade erosionsskydd.
• Samverka med nationella myndigheter, regioner, kommuner, fastighetsägare, privata sektorn och civilsamhället, internationella nätverk, och andra berörda aktörer.
• Initiera och bedriva forskning och utveckling inom ämnesområdet i samverkan med andra myndigheter, länsstyrelser, kommuner, universitet, högskolor och företag.
• Ta fram vägledningar och bidra till att utveckla geotekniska standarder för erosionsbedömningar och utformning av naturanpassade erosionsskydd.
• Förmedla kunskap via kurser, konferenser och seminarier.
• Stödja SGI:s uppdrag inom alla våra tre verksamhetsområden (klimatanpassning, effektivt markbyggande och renare mark).
• Stödja SGI:s verksamhet som remissinstans i plan- och byggprocesser.
Kvalifikationer
Vi söker dig som är civilingenjör eller har examen inom väg- och vattenbyggnadsprogrammet, samhällsbyggnadsteknik, naturgeografi eller geovetenskap, eller för tjänsten annan relevant utbildning av motsvarande nivå som av oss bedöms lämplig. För tjänsten krävs goda kunskaper om strömning i vattendrag samt erosionsprocesser. Du ska kunna uttrycka dig väl i tal och skrift på både svenska och engelska. Vi ser gärna att du har 5-10 års, eller mer, relevant arbetslivserfarenhet.

Meriterande för tjänsten är forskarutbildning. Vi ser gärna att du har god kunskap om dimensionering av erosionsskydd i vattendrag och geotekniska krav och standarder (t ex Eurocode, TK Geo) och erfarenhet av naturbaserade lösningar. Djupare kunskap inom numerisk modellering är också meriterande, likaså erfarenheter av att bedöma och beräkna vattnets förändringar i ett framtida klimat.

Du behöver vara lösningsorienterad, ha god samarbetsförmåga, men också kunna arbeta självständigt och ta egna initiativ. Vid urvalet kommer stor vikt att läggas vid din personliga lämplighet.
För att kunna arbeta hos oss ska du dela statens gemensamma värdegrund, http://www.sgi.se/sv/om-sgi/sa-arbetar-i/vardegrund-och-kompass/
Tjänsten är placerad vid enheten Stranderosion, Avdelningen för Georisker och geodata i Linköping, Göteborg eller Stockholm. Andra placeringsorter kan eventuellt diskuteras. Tjänsten är en tillsvidareanställning. Provanställning kan komma i fråga. Tillträde snarast enligt överenskommelse.
Kontaktpersoner
Per Danielsson Enhetsansvarig Stranderosion031 7496582, Mats Eriksson Avdelningschef Georisker och geodata 08 57845519. Fackliga kontaktpersoner: Eva Albin ST013-20 18 29, Mattias Andersson SACO013- 20 18 88
Ansök via denna länk på SGI´s hemsida:
https://recruit.visma.com/spa/sv/public/apply?guidAssignment=628ca272-2185-45d8-ab19-0bc5d300cc8d&description=True&forcelocale=true Visa mindre

About the position
Clinical Manufacturing & Supply (CM&S) is accountable for the supply of medicines to AstraZeneca’s clinical trials and toxicology studies. Clinical supply chains are amongst the most complex of any industry and our customers are increasingly demanding more speed and agility, as well as management of complex device supply chains and new modalities, without compromising quality or risk, so we need well-managed, fit-for-purpose systems to meet these challenges. The Digital & Lean function within CM&S are responsible for the systems used within clinical supply chain and the linked master data to enable planning, manufacture, pack and label to occur according to GMP.

Responsibilities
What you’ll do
Within CM&S we currently use the SmartSupplies systems suite and this is a global platform comprising of both GXP & non GXP applications to support key clinical supply chain activities including planning, manufacture, release, inventory management, labelling, traceability, shelf life management and reporting. The Inventory Manager will support CM&S staff to create, manage and maintain high quality project and system data according to Good Manufacturing Practise (GMP) standards. This will require a broad range of system and business process knowledge and skills.

The role holder will support inventory management across all Clinical Supply Chains including but not limited to:
• Lead business activities related to creating and managing external inventory in AZ for all drug projects. This include system (AZ SmartSupplies), business process (relevant SOPs), data management (any necessary changes to existing data) and appropriate communication to relevant stakeholders.
• Perform study set up activities in Smart Supplies system via digital inventory process and during this convert clinical study design in to kit design.
• Responsible for creation of items masters and lots in to AZ SmartSupplies PMD and will also manage updates to already set up items/lots including shelf life updates and correction of quantities.
• Lead Data Quality Maintenance activities including cycle count and periodic auditing of all inventory related records.
• Provide global leadership within the Item Master network to ensure that we continue to create and maintain, high quality item masters across both internal and external drug substance, drug product and packing activities.
• Develop and provide training in inventory management to relevant parties.
• Support Clinical Manufacture and Supply organization with problem solving.

In addition to the above and based on business needs there are also element of SmartSupplies system management in scope for the role
• Support User System Access
• Support system maintenance activities
• Support system validation Testing

Your profile
Essential for the role
• College/university degree in Science/Engineering
• A track record of working with and managing data changes in GxP systems
• Experience of the AZ Clinical Supply Chain systems environment, including SmartSupplies or equivalent commercial systems eg SAP
• Experience and familiarity with Clinical or Commercial supply chain processes
• Highly numerate, supported by strong computing skills
• Demonstration of high attention to detail
• Experience of effective working in a multi-cultural team
• Proven analytical and strategic thinking
• Good pedagogic skills to be able to train others
• Demonstrated good time and stakeholder management skills & flexibility to adapt to changing customer need
• Excellent English, both verbally and written

Desirable for the role
• Experience of drug substance or drug product development
• Conceptual thinking and experience of strategic frameworks
• Experience of lean / lean leadership / lean thinking
• Experience of agile development

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for 8 months. During this time you will be employed by QRIOS.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we are opening new ways to work, pioneering ground-breaking methods and bringing unexpected teams together. Interested? Come and join our journey. Visa mindre

About the position
We now have the opportunity for a consultant to join our team in the role as Analytical Scientist within the department Oral Product Development at AstraZeneca Gothenburg.
The assignment is to 31 Dec 2023.

Responsibilities
We are looking for a scientist in Analytical Chemistry who can provide input in the area of
analytical science during the development of drug products, and can work together with us
determining the quality attributes during the development of the formulations. The work includes
analytical testing , documentation, and attending and presenting in project team meetings. The
role is primarily laboratory based.

Your profile
Minimum requirements:
BSc or MSc typically from pharmaceutics, chemistry or analytical science, but also other
disciplines with relevant skills. Good knowledge in written and spoken English is necessary as
well as Scientific knowledge within analytical science, laboratory experience including working
with computerized systems and chromatography techniques (e.g. UPLC) for detection of small
molecules. If you have experience from working within the pharmaceutical industry, this will be
an advantage.

Desirable requirements:
As a person, you should be well organized, analytical, flexible and accurate. Good team working
skills are also important, together with the ability to operate independently. Good communication
skills linked to the ability to work to tight timelines are highly valued. If you have experience from
working in a GMP environment or worked in AstraZeneca or pharmaceutical industry, this will be
an advantage.

About the organisation
This is a consultant assignment at AstraZeneca in Göteborg until 2023-12-31.
During this time you will be hired by QRIOS.

QRIOS can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

About the position
Do you have experience of working with Regulatory Information and would like to work in a global team environment? Are you interested in a new challenge in the ever-changing environment called RIM (Regulatory Information Management)? Then this role is something for you!

We are now looking for a Regulatory Information Manager to join us in Global Regulatory Operations (GRO).

As an industry-leading Oncology Regulatory function, we drive efficiency and innovation to bring medicines to patients as quickly as possible. It’s by delivering rapid and global approvals, that we play our part in turning meaningful innovation in drug development strategies into reality. We play a key role in making sure our transformative science born in labs will be transformed into real value for patients.

Collaboration and learning are a big part of how we work and how we win. Within Regulatory we work together across our locations, therapy areas and external community to share learnings and knowledge. It means we are proactive self-starters, comfortable stepping up and taking ownership to enhance our personal and professional development.

We are all compassionate team players and driven achievers, always ready to step up. We are now looking for you who recognise yourself in this and want to join us taking on the Manager Regulatory Information role.

What you’ll do
The Regulatory Information Manager is responsible for supporting the management, collection, creation and analysis of regulatory data and regulatory information. The Regulatory Information Manager is an expert in end-to-end Regulatory Information Management (dossier format, publishing, tracking).

Responsibilities
Main responsibilities:
• Represents and manage the interface between Global Regulatory Operations (GRO) delivery units and early as well as late stage drug projects.
• Collaborates with GRO teams and partners to assure efficient delivery of end to end Regulatory Information Management.
• Manage and govern the regulatory data for assigned areas of responsibilities in accordance with regulatory data standards, business processes and regulatory requirements.
• Compiles and delivers XEVMPD, IDMP or other regulatory data submissions to health authorities.
• Develops self in topic areas critical to successful delivery of the RIM remit. Particularly, technical skills and knowledge of international regulations.
• Engages with partners, affiliates, or other customers and stakeholders to manage regulatory data and to ensure compliance with procedures and standards.
• Monitors the environment for changes in legislation related to regulatory information. Reviews and evaluates regulations, guidelines and technical specifications related to regulatory information processes and regulatory information data standards.
• Subject matter expert in the management, analysis and quality control of regulatory data standards and regulatory information.

Your profile
Essential for the role
• University degree in the life sciences or equivalent experience in pharmaceutical/medical industry
• Knowledge of pharmaceutical drug development process
• Strong analytical and critical thinking ability

Desirable for the role
• Good problem and conflict resolution skills.
• Ability to set and manage priorities, performance targets and project initiatives.
• Ability to innovate best practices with business process analysis and design

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg until 2024-05-24. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we are opening new ways to work, pioneering ground-breaking methods and bringing unexpected teams together. Interested? Come and join our journey. Visa mindre