Lediga jobb QRIOS AB i Göteborg

Are you a machine learning engineer or scientist excited by building and scaling modern AI systems for real-world impact? Do you want to enable the training and inference of large-scale deep learning models for drug discovery? We are seeking a 15-month consultant to join the innovative MolecularAI department at AstraZeneca in Gothenburg, Sweden.

Reponsibilities
You will drive impact across multiple projects with a focus on AI engineering and platform development. Your responsibilities will include:
• Optimize the training and inference of large-scale deep learning models for drug design on state-of-the-art HPC platforms
• Design, conduct and evaluate scientific experiments together with our multi-disciplinary research team to help us build the next generation of foundational chemical models.
• Extend and maintain scientific codebases written in Python that forms the backbone of our AI platforms. See https://github.com/molecularai/
• Collaborate cross-functionally with researchers in data science, software engineers and drug discovery domain experts
This is an on-site role based in Gothenburg, Sweden where you expect to present on site three days per week.

Your profile
Essential Qualifications
We believe you are passionate about building engineering solutions for life sciences. You have:
• Degree in computer science, engineering, chemistry, physics, mathematics or related discipline, or equivalent industry experience
• Hands-on experience training models with PyTorch or equivalent frameworks
• Excellent programming skills, preferably in Python. Track record of developing sizable software solutions and familiarity with scientific packages (Numpy, Pandas, etc.)
• Proven ability to work inclusively within multidisciplinary teams, with a focus on building a positive and collaborative team culture.

Desirable requirements
You would benefit from having experience or familiarity with:
• Experience with high-performance computational platforms and schedulers such as SLURM
• Experience writing ETLs for large data sets
• Background in life sciences or physical sciences
• Research and outreach contribution to open-source projects, publications, or participation in online communities

About the Organisation
This is a consultant assignment at AstraZeneca in Göteborg for 15 months, starting in April 2026.
During the time you will be hired by QRIOS.
Please apply by registering your CV here on our website. Click on the "Ansök" button to the right. It is our recommendation that you register as much information as possible and that you attach a complete CV-document. Please check that your correct e-mail address is registered. Visa mindre

Our Genome Engineering Team in Gothenburg, Sweden focuses on developing treatment for Rare Diseases. We continually push the boundaries of science to expand the limits of scientific research to better understand rare diseases, discover new life-changing treatments and deliver medicines to patients.

As a Senior Research Scientist, you will be a key member of the Genome Engineering Department. You will join our international team that develops novel genome engineering technologies and applies these breakthroughs to generate innovative gene therapies. We provide a stimulating environment with state-of-the-art facilities where you can transform cutting-edge genome engineering tools into effective and safe medicines.

About the position
In this laboratory-based role, you will leverage your scientific expertise in genome engineering and innovative thinking to develop novel tools and applications that can lead to breakthrough therapies. As a key member of cross-functional project teams, you will develop and evaluate genome editing strategies for specific disease projects. Accountabilities will include innovative optimization of genome engineering technologies to facilitate effective gene editing in target cell & tissue types, developing relevant assays, analyzing gene editing outcomes, documenting, interpreting, and communicating results to appropriate partners.

Reponsibilities
• Establishing and maintaining disease cell models using immortalized or iPSC cell lines
• Establishing and running cellular and biochemical assays to evaluate efficacy of therapeutic genome editing approaches in disease models
• Documenting, interpreting and communicating results to stakeholders and partners

Your profile
Essential for the role:
• PhD degree in molecular cell biology or relevant areas with strong wet-lab skills, or MSc degree with equivalent experience
• Experience with handling and differentiating iPSCs to different cell types (e.g. liver, heart)
• Track record of establishing high-quality cellular assays (e.g. viability, metabolic activity, protein quantification, flow cytometry, microscopy)
• Strong communication skills, scientific rigor and ethics, ability to effectively work independently and collaboratively in a team

Desirable for the role:?
• Experience in metabolism research
• Understanding and previous hands-on experience with CRISPR-Cas9 technologies
• Hands-on experience with standard molecular biology approaches for quantifying protein levels (e.g. Western blot, ELISA) or measuring protein activity
• Experience working with lentiviral vectors for engineering cell models

About the Organisation
This is a consultant assignment at AstraZeneca in Göteborg for 1 year, starting mid of April 2026.
During the time you will be hired by QRIOS.
Please apply by registering your CV here on our website. Click on the "Ansök" button to the right. It is our recommendation that you register as much information as possible and that you attach a complete CV-document. Please check that your correct e-mail address is registered. Visa mindre

Join the Bioscience Immunology team within Research and Early Development, Respiratory & Immunology. You will support in vitro studies, and ex vivo analyses on mouse cells, focusing on inflammatory and autoimmune diseases. Respiratory & Immunology is one of AstraZeneca’s core therapy areas, aiming to understand, treat, modify, and ultimately cure respiratory and autoimmune diseases.

Reponsibilities
• Plan and execute experiments: Design, perform, and analyze in vitro and ex vivo studies to advance drug discovery projects and generate publishable insights.
• Contribute scientifically: Engage in study design discussions and data interpretation; present findings, rationale, and recommendations.
Accountability:
• Hands-on work: Conduct in vitro and ex vivo analyses from rodent studies alongside a team of committed scientists.
• Data responsibility: Uphold the highest standards of data integrity, quality control, and archiving.
• Communication: Evaluate and interpret primary data; write reports and summaries; present in team and project meetings.

Your profile
Essential for the role:

• Master’s in biology or related field
• Flow cytometry expertise: At least 5 years’ experience with routine FACS on mouse samples, including organ processing/digestion, staining, antibody panel design; proficiency with BD FACSDiva instruments and FlowJo.
• Cellular/molecular techniques: Ability to independently plan, execute, and analyze protein expression/activation assays (ELISA, Western blot, Meso Scale Discovery) and RNA analysis (extraction, qRT PCR).
• Data and statistics: Understanding of statistical methods, quality control, reporting, and data archiving.
• Communication: Excellent written and spoken English; strong presentation skills.

Desirable for the role:

• PhD in immunology; deep understanding of autoimmune diseases, especially gut, skin, or joint immunology.
• In vivo experience: Familiarity with animal models of inflammation/autoimmunity.
• Cell isolation and sorting: Experience with column-based cell isolation (e.g., MACS, StemCell Technologies) and FACS-mediated cell sorting.
• Cell culture: Experience with murine leukocytes in vitro assays.

About the Organisation
This is a consultant assignment at AstraZeneca in Göteborg from March until October 2026. During the time you will be hired by QRIOS.
Please apply by registering your CV here on our website. Click on the "Ansök" button to the right. It is our recommendation that you register as much information as possible and that you attach a complete CV-document. Please check that your correct e-mail address is registered. Visa mindre

Join the Bioscience Asthma & Skin Immunity in vivo team within Research and Early Development, Respiratory & Immunology. You will support in vitro and in vivo studies, and ex vivo analyses. Respiratory & Immunology is one of AstraZeneca’s core therapy areas, aiming to understand, treat, modify, and ultimately cure respiratory and autoimmune diseases.

Reponsibilities
What you will do:
• Plan and execute experiments: Design, perform, and analyze in vitro and ex vivo studies to advance drug discovery projects and generate publishable insights.
• Support in vivo experiments

Accountabilities:
• Hands on work: Conduct in vitro and ex vivo analysis from rodent studies alongside a team of committed scientists; support in vivo scientists with preparations for experiments, collecting biological samples and live animal handling.
• Data responsibilities: Uphold the highest standards of data integrity, quality control, and archiving.
• Communication: Evaluate and interpret primary data; write reports and summaries; present in team and project meetings.

Your profile
Essential for the role:
• Cellular/molecular techniques: Ability to independently plan, execute, and analyze protein expression/activation assays (ELISA, Meso Scale Discovery) and RNA analysis (extraction, qRT PCR).
• In vivo experience: Hands-on experience with rodents including live animal handling, drug administration through different routes, blood and organ sampling and processing. Valid education required for compliance to work with live animals in Sweden (LAS, FELASA)
• Data and statistics: Understanding statistical methods, quality control, reporting, and data archiving.
• M.Sc. degree in relevant subjects or equivalent level of understanding developed through experience in academia or drug discovery settings.

Desirable for the role:
• Experience in lung function measurements in rodents

Soft skills:
• Communication: Excellent written and spoken English
• Strong presentation skills.

About the Organisation
This is a consultant assignment at AstraZeneca in Göteborg from April until end of 2026. During the time you will be hired by QRIOS.
Please apply by registering your CV here on our website. Click on the "Ansök" button to the right. It is our recommendation that you register as much information as possible and that you attach a complete CV-document. Please check that your correct e-mail address is registered. Visa mindre

Are you an experienced scientist with great expertise in Next Generation Sequencing and Molecular Biology? Do you want to use this expertise to contribute to the discovery of novel oligonucleotide therapies? We have an opening suitable for you!

Right now, we are looking for a passionate and hard-working Molecular Biologist with NGS skills to join our NGS & Transcriptomics function within the Centre of Genomic Research Department at AstraZeneca in Gothenburg, as one of our group members is going on parental leave. You will contribute with your expertise in applying molecular biology and NGS to the discovery of novel oligonucleotide therapies.

AstraZeneca’s ambition is to become world-leading in in the field of oligonucleotide therapies. We are achieving this through advances in oligonucleotide science and innovation internally and through the establishment of key collaborations outside AstraZeneca. To this end, we currently have a portfolio of very high-profile projects at different phases of drug discovery within AstraZeneca, and you will directly contribute to their successful progression to oligonucleotide therapies.

Responsibilities
This lab-based role is for a Molecular Biologist with significant NGS expertise, which you will apply to the characterization and profiling of the effects of oligonucleotide treatments in in vitro and in vivo cellular assays and models in support of novel drug discovery projects.
Our team is a collaborative group, and you will engage in the supervision and mentorship of other scientists, ensuring that methods run expertly and accurately, developing and guiding the setup of new techniques. Included in the role is also to nurture strong collaborative relationships with the project investigators, key partners, and data scientists to ensure the smooth running of projects.

About the organisation
This is a consultant assignment for 1 year at AstraZeneca in Göteborg.
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.

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

På uppdrag av vår världsledande samarbetspartner söker vi nu en driven och erfaren forskningssjuksköterska i Mölndal.
I rollen ingår att ta hand om deltagare i olika studier, både kliniska och icke-kliniska samt att arbeta med att planera och
genomföra studierna. Studierna görs med intresse att utveckla nya hälsofrämjande produkter.

Vem är du?
För att ha rätt förutsättningar i rollen ser vi att du har:

• Sjuksköterska med minst 3 års erfarenhet från kliniska prövningar eller andra tester på
människor, eller annan relevant utbildning och vana av att ha arbetat med kliniska studier eller andra tester/forskning med människor.
• Mycket goda kunskaper i både svenska och engelska.

Vi ser gärna att man har följande personliga egenskaper:
• Noggrann, problemlösare och förmåga att ta egna initiativ.
• Kan jobba brett med varierandearbetsuppgifter inom olika delar av utveckling och testning av produkter.
• Social personlighet och god förmåga att kunna kommunicera både i tal och skrift med såväl interna som externa uppdragsgivare och kunder, samt privatpersoner i form av studiedeltagare.

Om verksamheten
Detta är ett konsultuppdrag hos kund i fram till december 2026. 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

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

Desirables:
• 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)

Soft skills:
• Strong in?uencing, negotiating and problem-solving skills, across geographical and cultural boundaries
• Ability to adapt and operate in bespoke multiple systems.

About the organisation
This position is a consultant assignment at AstraZeneca for 12 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 Visa mindre

Är du en säljdriven relationsbyggare med erfarenhet från konsultbranschen?
Vill du vara med och växa vår verksamhet inom Life Science i Göteborg?
QRIOS Life Science söker nu en engagerad konsultchef som vill kombinera kundansvar, rekrytering och ledarskap – med tydligt fokus på affären.

Om tjänsten
Som konsultchef har du en central roll i att driva vår tillväxt i regionen. Du ansvarar för försäljning, rekrytering och att coacha konsulter i uppdrag. Rollen passar dig som gillar att skapa affärer, utveckla relationer och bygga team i ett högt tempo.
Vår vision är att stödja och driva innovation genom att förse våra kunder med högkvalitativa och skräddarsydda konsulttjänster. För att ytterligare stärka vårt team söker vi nu en engagerad och resultatinriktad konsultchef.

Dina arbetsuppgifter i huvudsak
• Driva nyförsäljning och utveckla kundrelationer inom Life Science.
• Rekrytera och matcha rätt konsulter till rätt uppdrag.
• Leda och stötta konsulter i deras utveckling.
• Bidra till affärsutveckling och lönsamhet.
• Vara en närvarande aktör i branschens nätverk i Göteborg.

Vem är du?
• Har 2–3 års erfarenhet av B2B-försäljning inom konsult- eller bemanningsbranschen.
• Trivs i rollen som både säljare och ledare.
• Har god kännedom om Life Science-marknaden i Västsverige.
• Är målinriktad, engagerad och strukturerad.
• Har akademisk bakgrund och talar flytande svenska och engelska.

Om verksamheten
Välkommen med din ansökan senast den 25e juni.
Urval sker löpande – skicka in ditt CV och personliga brev redan idag!

Vi erbjuder
En dynamisk roll med stort handlingsutrymme och möjlighet att bygga din egen affär. Du blir en del av ett kompetent team i ett bolag med tydlig position och stark kultur. Vi erbjuder konkurrenskraftiga villkor och goda utvecklingsmöjligheter – både affärsmässigt och personligt.

Om QRIOS
QRIOS är ett värderingsdrivet konsultbolag där Passion & Execution genomsyrar allt vi gör. Vi tror på handlingskraft, ansvar och att växa tillsammans. Med ett starkt fäste inom Life Science är vi redo att ta nästa steg i Göteborg – och vi vill ha dig med på resan.

QRIOS MINDS GÅR LÄNGRE. Visa mindre

We are now recruiting a Senior Scientist to join the Automation & Assays team in Bioscience technology within
Early Cardiovascular, Renal and Metabolism (Early CVRM) in our dynamic R&D site in Gothenburg, Sweden
The Automation & Assay team using advance automation platforms for molecular biology assays to enable delivery
of high-quality data to build a detailed understanding of pharmacological response and mode of action for e.g. small
molecules, oligos, antibodies as therapeutic drugs in our pipeline projects across the Cardiovascular, Renal and Metabolism disease areas.

About the position
As a Senior Scientist you will primarily process tissue samples using cell surface protein enrichment techniques for proteomics to provide experimental support to our drug discovery programs, development and characterisation, and
optimisation of new models.
There will be possibility to be part of building automated methods for sample preparation
for proteomics analysis.

Responsibilities
• Tissue samples using cell surface protein enrichment techniques for proteomics
• Potentially take part in the assay and method development using advanced automated platforms
• Independent planning and execution of experiments, troubleshooting and timely reporting/presentation of data
according to agreed timelines.
• Join further model development activities to support drug projects with biomarker and molecular assays for
resolving mechanisms of action, target identification, and candidate drug evaluation.
• Effectively communicate and collaborate across the Early CVRM and with the key stakeholders in other
functions.

Your profile
Essential Requirements:
• For the Senior Scientist role: PhD or a master’s degree + 4 years of relevant experience
• Background in Molecular Biology, Biomedical, Pharmacology, Biochemistry or a related discipline with significant practical experience.
• Extensive experience in molecular and cellular biology techniques and in particular protein assays and sample preparation
• Independent study design, laboratory work, and data analysis
• Excellent communication skills in English, both verbal and in writing

Desirable Experiences and abilities:
• Processing of biological samples for proteomic analysis
• Knowledge in Proteomics
• Independent technical capability with assay development
• Innovative mindset with a drive for scientific excellence and continuous improvement.
• Experience in automation technology such as robotic liquid handler
• Proven ability in providing technical leadership and guidance to others.
• Experience from pharmaceutical industry
• Scientific visibility and leadership through project contributions and scientific publications.

Soft skills:
• Effectively communicate and collaborate in a matrix team setting to implement technical solutions
• Excellent interpersonal skills and excellent communication skills in English, both verbal and in writing
• Strong ability to engage and collaborate across boundaries with a problem-solving attitude and focus on delivery

About the organisation
This position is a consultant assignment at AstraZeneca for 12 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 Visa mindre

We are now recruiting a Scientist to join the Automation & Assays team in Bioscience technology within Early Cardiovascular, Renal and Metabolism (Early CVRM) in our dynamic R&D site in Gothenburg, Sweden

The Automation & Assay team using advance automation platforms for molecular biology assays to enable delivery of high-quality data to build a detailed understanding of pharmacological response and mode of action for e.g. small molecules, oligos, antibodies as therapeutic drugs in our pipeline projects across the Cardiovascular, Renal and Metabolism disease areas.

About the position
As a Scientist you will primarily process tissue samples using cell surface protein enrichment techniques for proteomics to provide experimental support to our drug discovery programs, development and characterisation, and optimisation of new models. There will be possibility to be part of building automated methods for sample preparation for proteomics analysis.

Responsibilities
Responsibility includes:
• Tissue samples using cell surface protein enrichment techniques for proteomics
• Potentially take part in the assay and method development using advanced automated platforms
• Planning and execution of experiments, troubleshooting and timely reporting/presentation of data according to agreed timelines.
• Join further model development activities to support drug projects with biomarker and molecular assays for resolving mechanisms of action, target identification, and candidate drug evaluation.

Your profile
Essential Requirements:
• For the Scientist role: Master’s degree + 2 years of relevant experience.
• Background in Molecular Biology, Biomedical, Pharmacology, Biochemistry or a related discipline with significant practical experience.
• Extensive experience in molecular and cellular biology techniques and in particular protein assays and sample preparation
• Independent study design, laboratory work, and data analysis
• Excellent communication skills in English, both verbal and in writing

Desirable Experiences and abilities:
• Processing of biological samples for proteomic analysis
• Potential knowledge in Proteomics
• Independent technical capability with assay development
• Experience in automation technology such as robotic liquid handler
• Proven ability in providing technical leadership and guidance to others.
• Experience from pharmaceutical industry

Soft skills:
• Effectively communicate and collaborate in a matrix team setting to implement technical solutions
• Excellent interpersonal skills and excellent communication skills in English, both verbal and in writing
• Strong ability to engage and collaborate across boundaries with a problem-solving attitude and focus on delivery

About the organisation
This position is a consultant assignment at AstraZeneca for 12 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 Visa mindre

Mölnlycke Health Care is a world-leading provider of single-use surgical and wound care products for customers, healthcare professionals and patients. We develop and bring to market innovative wound care and surgical products along the entire continuum of care – from prevention to post-acute settings. Our solutions provide value for money, supported by clinical and health economic evidence.

About the position
I am searching for a Physical Testing Laboratory Engineer within projects and platforms for a consultant assignment that will start in October 2025.

In this position you will be part of a dynamic and skilled laboratory team. You will work together with colleagues from different R&D disciplines to deliver the product development milestones in innovation projects. You will be responsible for planning and performing your assigned laboratory deliverables in different projects. Relevant test areas are physical testing, including analysis of adhesion and fluid handling properties in wound care products.
You are curious to learn new areas and techniques. You have also a flexible mindset and are able to adapt to a dynamic environment with short lead times.

Applications will be evaluated continously and the position may be filled before the end date. Submit your CV and personal letter today!

Your profile
We expect you to have:

• Master’s degree or Bachelor’s degree in engineering, preferably within physics, material, biomedical or equivalent
• Relevant laboratory work experience
• Fully trained according to Lab Engineer and assigned roles according to training Matrix
• Knowledge in working with development and validation of test methods and instruments
• Basic understanding of Global Regulatory Requirements and standards related to medical device
• Basic understanding in Design control
• Technical competence in laboratory methods
• Fluent English written and spoken
• Communication skills

About the organisation
This is a consultant assignemt at Mölnlycke Health Care for 24 months, starting in October 2025. 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. Being a consultant at QRIOS gives you opportunities to try different industries, companies and roles. Visa mindre

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.

About the position
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
This is an exciting role where you will act as a key member of various project teams and provide your technical and scientific expertise into formulation design of biomacromolecules within the new modality area. As a Scientist you will support drug projects from a formulation perspective in the discovery phase of the drug development process, working from target identification to candidate drug nomination. The role covers development and characterization of formulations of oligonucleotides of high complexity. You will support drug projects within your own function in the preclinical phase and you will serve as a member of the cross-functional drug development project teams, representing your function and scientific area. You will work in close collaboration with formulation scientists, analytical chemists as well as biopharmaceutics experts in Gothenburg, Sweden but also with colleagues in Cambridge, UK and Waltham, US.

Your profile
Essential for the roles
• Masters or PhD degree in relevant scientific discipline (e.g., Analytical Chemistry, Biochemistry, Biotechnology or Pharmacy)
• Previous experience of working with biomacromolecules (e.g. RNA, proteins or peptides) or formulations of small molecules.
• Ability to work independently in a laboratory setting

Desirables:
• Industrial experience in a pharmaceutical environment.

Soft skill:
• Scientific interest in exploratory formulation/characterization work related to complex molecules, delivery systems and new technologies.
• Ability and desire/willingness to effectively communicate, network and build collaborative relationships with partners across disciplines?and cultures, internally and externally and independently lead and influence projects.

About the organisation
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

This is a consultant assignment at AstraZenca in Göteborg from May until end of December 2025. During this time you will be hired by us at QRIOS. Visa mindre

At AstraZeneca, our achievements stem from scientific excellence. Our innovative work thrives on collaboration, ensuring that every member of our team understands how their role contributes to our broader mission of showcasing the power of science.
The NGS/Transcriptomics team is a dynamic group dedicated to advancing “omics” technologies and methodologies. Our goal is to generate insightful data that enhances our understanding of drug pharmacology, target mechanisms, model systems, patients, and diseases, aligning closely with AstraZeneca’s strategy for Growth through Innovation.
We are seeking a Research Scientist with a background in molecular biology laboratory practices. The ideal candidate will possess exceptional teamwork skills and a history of collaborative success to drive scientific excellence and deliver robust results for our research projects.

About the position
This role is for a lab-based Research Scientist with knowledge and experience in transcriptomics / proteomics. This is a hands-on laboratory-based role with focus on effective delivery to support various clinical and preclinical projects across multiple diseases, species and drug modalities.

Responsibilities
• Utilize prior practical laboratory experience in transcriptomics/proteomics data generation with a strong emphasis on automation technologies.
• Contribute to planning and execution of projects involving new omics technologies, integrating automated solutions to enhance efficiency and precision.
• Develop and implement innovative automated processes to streamline the workflows.
• Maintain laboratory processes and equipment rigorously, ensuring efficient operation and performance of automated systems and workflows.
• Provide experimental support to fellow team members, promoting a collaborative environment and help implementing high-throughput workflows.
• Ensure compliance with Safety, Health, and Environmental regulations as well as AstraZeneca’s corporate responsibility policies.
• Develop a comprehensive understanding of the pharmaceutical industry and identify opportunities for new business initiatives.
• Collaborate with a wide range of scientists from different backgrounds to ensure the highest quality of research.
• Develop and validate cutting edge protocols for the simplification of multiomic research through automation.

Your profile
Essential for the role:
• Masters degree or higher in a relevant scientific discipline and/or equivalent demonstrated experience in a relevant academic or industry environment.
• A strong understanding of molecular biology theory and techniques.
• Hands-on experience with at least one Next Generation Sequencing/Transcriptomics/Proteomics technology (NGS based proteomics technology, RNA-seq, DNA-Seq, Genotyping methodologies, mass spectrometry).
• Experience with automation technologies and integrating them into routine laboratory practices.
• Excellent organizational and communication skills.

Desired Qualifications:
• Extensive research experience in Pharma/Biotech, medical, or academic environments.
• A record of high-quality peer-reviewed publications or scientific presentations.
• Experience in laboratory automation utilising automated liquid handlers or scheduling engines.
• Experience in operating in a regulated environment such as GLP or ISO15189
• Demonstrated expertise in statistics, quantitative data analysis, data mining, and familiarity with LIMS (Laboratory Information Management Systems).

About the organisation
This is a consultant assignement at AstraZeneca Göteborg for 1 year starting in June 2025. 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

På uppdrag av vår världsledande samarbetspartner söker vi nu en driven och erfaren laboratorieingenjör med intresse att utveckla nya hälsofrämjande produkter. Den rätta kandidaten skall ha praktisk erfarenhet av att arbeta med olika material och fysikaliska provtagningar. 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

Har du erfarenhet från tidigare chefsroller och redo för nästa utmaning i arbetslivet? Vi söker nu en chef till vår Processteknik- och Utvecklingsavdelning på St1 Refinery AB. 
OM TJÄNSTEN
Som chef för Processteknik och Utveckling har du övergripande ansvar för vår processtekniska uppföljning och utveckling. På avdelningen arbetar 7 processingenjörer och en APC ingenjör som du ansvarar för. I rollen leder du gruppen mot uppsatta mål, coachar dina medarbetare till att vara sitt bästa jag och tillser att gruppen levererar enligt förväntan. Tjänsten är placerad på vårt raffinaderi som är beläget på Hisingen, precis vid Älvsborgsbron.
Huvudsakliga ansvarsområden/arbetsuppgifter:

Leda arbetet med att optimera den dagliga driften genom nära samarbete med driften.


Driva processutvecklingen av vårt raffinaderi genom IMP (investment management process), där du har en aktiv roll.


Driva samarbetet med våra partners som licensgivare samt inom engineering.


Prioritera och besluta om åtgärder för anläggningarna tillsammans med avdelningarna för drift, supply, inspektion, laboratorium och underhåll.


Vara en nyckelspelare inom arbetet med företagets utsläppshandel.


Tillse att arbetet genomförs enligt lagar och rutiner med avseende på hälsa, säkerhet, miljö och kvalitet.


Följa upp arbetet avseende dokumentation och ekonomi.


Din grupp:

Optimerar raffinaderiets anläggningar utifrån produktkvalitet, säkerhet, hälsa, miljö, energieffektivitet och ekonomi. Både kort- och långsiktigt


Månatliga och årliga miljörapporteringar, däribland CO2- och NOx-utsläpp.


Är utredare i projekt och genomför provkörningar av raffinaderiets anläggningar


Mäter och beräknar inom ramen för given miljölagstiftning samt rapporterar inom ramen för utsläppshandel


Utvecklar och optimerar applikationer för processkontroll av våra anläggningar på raffinaderiet


Beräknar, simulerar och utvärderar projekt för nya anläggningar samt utbildar personal i processtekniska frågor


Budgetera, planera och samordna förstudier för förbättrings- och omställningsprojekt


DIN PROFIL
För att lyckas och trivas i denna roll så ser vi att du har erfarenhet från tidigare chefsroller där du lett en ingenjörsgrupp. Vi ser att du har en?civilingenjörsexamen inom exempelvis?kemiteknik eller motsvarande erfarenhet. Erfarenhet från processindustrin ser vi som meriterande. Du kan uttrycka dig obehindrat på svenska och engelska, både i tal och skrift.
Vi söker dig som gillar att ta eget ansvar och initiativ och trivs att jobba i en organisation med korta beslutsvägar. Du uppskattar ett stundtals högt tempo och stimuleras av att arbeta i en bransch som befinner sig i en förändringsresa. Då arbetet präglas av samarbete och interaktion med både interna och externa kollegor förutsätter vi att du har gott ordningssinne och samarbetsförmåga. Du tycker om att leda och är intresserad av människor och deras utveckling. Denna roll ställer också höga krav på säkerhetsmedvetenhet och därför ser vi att du är en ansvarsfull person som alltid strävar efter att förbättra din, dina medarbetares och kollegors arbetsmiljö.
Vår personal är viktig för oss och vi har många förmåner som uppskattas bland våra anställda. Förutom kompetenta och engagerade kollegor så erbjuder vi ett spännande arbete med stora kontaktytor samt en platt organisation. Du har goda förutsättningar för att utvecklas vidare inom företaget i en bransch som är under stor förändring med flera?kommande spännande projekt. Övriga förmåner inkluderar:

Attraktiv bonus utöver din grundlön


Utfyllnad av föräldraförsäkring vid barnledighet


ATK (arbetstidsförkortning)


Andel i företagets vinstandelsstiftelse


Goda träningsmöjligheter på siten med ett nyrenoverat stort gym, uppvärmd pool och idrottshall


Friskvårdsbidrag och subventionerad företagshälsovård


Subventionerad lunchförmån och subventionerade aktiviteter där vi hittar på roliga saker tillsammans


Jeanette Gränsfelt, Teknisk chef:
”Det är roligt att gå till jobbet varje dag, ingen dag är den andra lik. St1 Refinery är en arbetsplats där du verkligen kan göra skillnad. Hos oss på tekniska avdelningen får du möjlighet att arbeta med ledarskap samtidigt som du får ta lead på våra tekniska utmaningar. Vi välkomnar oliktänkande medarbetare. Arbete genom ständiga förbättringar och utmaningar driver oss framåt.
I rollen som chef ska du tillsammans med ditt team arbeta för att optimera den dagliga driften, genomföra förstudier för att ta våra anläggningar in i framtiden och aktivt arbeta för energieffektivisering samt reducera våra utsläpp. Jag ser fram emot att få arbeta tillsammans med dig.” 
OM St1
Vi är ett nordiskt energibolag som vill vara med och driva energiomställningen och vår vision är att bli den ledande producenten och säljaren av CO?-medveten energi. För verksamheten i Sverige följer vi Sveriges klimatmål vilket innebär att vi senast 2045 ska ha nettonoll utsläpp. På vårt raffinaderi i Göteborg har vi ungefär 280 anställda med experter och specialister inom processindustrin med produktion och underhåll av anläggningen. Raffinaderiet är verksamt dygnet runt, året runt. Raffinaderiet är sedan 1997 miljöcertifierat enligt EMAS och ISO 14001. Vi investerar stort i biogas och driver också två stora projekt för att tillverka avancerade biodrivmedel respektive elektrobränslen för flyget. Vi startade vår första gröna anläggning nyligen som producerar biodiesel och vi håller också på att anlägga en solcellspark i Göteborg. Visa mindre

Har du erfarenhet av att leda människor inom processindustrin, kunskap inom roterande utrustning och är redo för nästa utmaning i arbetslivet? Då kan detta vara möjligheten för dig! Vi söker nu en chef till vår roterande avdelning på St1 Refinery AB.
OM TJÄNSTEN
Som chef för roterande avdelningen har du det övergripande ansvaret för vår roterande utrustning. Tjänsten ingår i underhållsavdelningen och du rapporterar direkt till vår Underhållschef. I arbetsuppgifterna ingår att budgetera, planera och samordna, både förebyggande och avhjälpande underhåll. På avdelningen arbetar en underhållsingenjör, en koordinator samt tio tekniker.
Huvudsakliga ansvarsområden/arbetsuppgifter:

Ta fram årlig budget


Leda arbetet med tillförlitligheten av vår roterande utrustning samt tillse att vår reservdelshållning är anpassad till utrustningens behov


Tillsammans med driftavdelningen och övriga delar av underhåll prioritera och besluta omfattning av reparationer och underhåll


Vara beställare och projektledare av projekt inom ansvarsområdet


Tillse att arbetet genomförs enligt lagar och rutiner med avseende på hälsa, säkerhet, miljö och kvalitet


Följa upp arbetet med avseende på dokumentation och ekonomi


Beredskapstjänst förekommer


DIN PROFIL

Erfarenhet från drift och / eller underhåll inom processindustri och med roterande utrustning ser vi som klart meriterande


Minst 5 års erfarenhet från arbete som chef inom processindustri


Teknisk högskoleutbildning med inriktning mot maskinteknik är meriterande


God kännedom om Microsoft Office


Vi söker dig som gillar att ta eget ansvar och egna initiativ samt trivs att jobba i en organisation med korta beslutsvägar och möjlighet att påverka. Då arbetet präglas av samarbete och interaktion med både interna och externa kollegor förutsätter vi att du har gott ordningssinne, samarbetsförmåga och kan uttrycka dig väl på både svenska och engelska. Du behöver också tycka det är roligt att arbeta i en bransch som befinner sig mitt i en förändringsresa. Viktigt för rollen är att du tycker om att leda och är intresserad av människor och deras utveckling. Att arbeta inom processindustrin ställer också höga krav på skyddsmedvetenhet och därför ser vi också att du är en ansvarsfull person som alltid strävar efter att förbättra din och dina kollegors arbetsmiljö.
Vår personal är viktig för oss och har många förmåner som uppskattas bland våra anställda. Förutom kompetenta och engagerade kollegor så erbjuder vi ett intressant och spännande arbete med stora kontaktytor samt en en platt organisation där kommunikations- och beslutsvägar är korta. Övriga förmåner inkluderar:

Attraktiv bonus utöver din grundlön


Utfyllnad av föräldraförsäkring vid barnledighet


ATK (arbetstidsförkortning)


Andel i företagets vinstandelsstiftelse


Goda träningsmöjligheter på siten med ett nyrenoverat stort gym, uppvärmd pool och idrottshall


Friskvårdsbidrag


Subventionerad företagshälsovård


Subventionerad lunchförmån


Subventionerade aktiviteter där vi hittar på roliga saker tillsammans


Henrik Teiffel, Underhållschef:
”Jag upplever att på St1 Refinery känner man sig alltid välkommen och det är alltid trevligt att komma till jobbet! Hos oss på underhållsavdelningen så finns det en nyfikenhet och öppet sinne för förändringar hos medarbetarna. Ställs vi inför utmaningar så hjälper vi varandra för att tillsammans arbeta lösningsfokuserat.
I rollen som chef roterande är det viktigt att vilja utveckla struktur och arbetssätt för att skapa ständiga förbättringar”
OM St1
Vi är ett nordiskt energibolag som vill vara med och driva energiomställningen och vår vision är att bli den ledande producenten och säljaren av CO?-medveten energi. För verksamheten i Sverige följer vi Sveriges klimatmål vilket innebär att vi senast 2045 ska ha nettonoll utsläpp. På vårt raffinaderi i Göteborg har vi ungefär 280 anställda med experter och specialister inom processindustrin med produktion och underhåll av anläggningen. Raffinaderiet är verksamt dygnet runt, året runt. Raffinaderiet är sedan 1997 miljöcertifierat enligt EMAS och ISO 14001. Vi investerar stort i biogas och driver också två stora projekt för att tillverka avancerade biodrivmedel respektive elektrobränslen för flyget. Vi startade vår första gröna anläggning nyligen som producerar biodiesel och vi håller också på att anlägga en solcellspark i Göteborg. Visa mindre

Är du den framtida ledare som vi söker för att växa och utveckla vår affär inom Life Science?
QRIOS Life Science söker nu en driven och engagerad Business Unit Manager med passion för att skapa tillväxt och utveckling inom vår verksamhet. Om du är en konsultchef med hög energi, drivs av affärer, rekrytering och ledarskap, och har ett intresse av strategier och verksamhetsutveckling, är detta chansen för dig att ta nästa steg i karriären!
QRIOS är ett värderingsdrivet bolag där våra värderingar, Passion & Execution, står för mer än bara ord. De påverkar vad vi gör och hur vi driver bolaget. Som ett värderingsdrivet bolag ger vi oss möjligheten att särskilja oss och skapa en unik förutsättning när det gäller att bygga ett bolag drivet av våra handlingar och beteende. Det är vi tillsammans som bygger kultur och värdegrund, inifrån och ut.
Om tjänsten
Som Business Unit Manager kommer du att ha en central roll i vår organisation, där du ansvarar för att driva vår B2B-försäljning av konsulter, utveckla strategiska kundrelationer, samt bygga ditt eget team av konsulter och konsultchefer på ett sätt som säkerställer lönsamhet inom ditt affärsområde. Du kommer att ha stor frihet att utveckla enheten och din affär, samtidigt som ditt ansvar som ledare ökar i takt med att bolaget växer.
Dina ansvarsområden

Försäljning av konsulter: Driva och utveckla försäljningen av konsulttjänster inom Life Science-sektorn.


Rekrytering och kundbearbetning: Ansvar för rekryteringsprocesser samt strategisk bearbetning och att vårda kundrelationer.


Ledarskap: Motivera och leda ditt team mot uppsatta mål, och säkerställa att både medarbetare och kunder är nöjda.


Affärsutveckling: Identifiera nya affärsmöjligheter och utveckla strategier för att expandera vår marknadsnärvaro.


Team Building: Bygga upp din verksamhetsdel från grunden och skapa ditt eget team.


P&L-ansvar för enheten.


Profilen vi söker har

Minst 3 års erfarenhet av B2B-försäljning av konsulter inom Life Science, med dokumenterad framgång inom området.


Erfarenhet av rekrytering och strategisk kundbearbetning.


Erfarenhet av ansvar för P&L. 


Relevant akademisk utbildning, gärna inom teknik eller naturvetenskap.


Flytande svenska och engelska, både i tal och skrift.


Som person är du inspirerande, har hög energi och är handlingskraftig. En förutsättning för att lyckas i rollen är att du har ett stort intresse för människor och teknik. Du är driven och visar vägen framåt för dina medarbetare genom att sätta upp tydliga mål och coacha dem i rätt riktning. Vidare är du inlyssnande och omtänksam och arbetar utifrån våra värderingar. Att både sälja och leda är en självklarhet för dig.
Vi erbjuder en dynamisk och utvecklande arbetsmiljö där du får möjlighet att påverka och forma vår framtid. Hos oss får du en roll med stort eget ansvar och möjligheter till både personlig och professionell utveckling. Vi erbjuder konkurrenskraftiga villkor och förmåner, samt chansen att vara en del av ett engagerat team med hög kompetens och stark sammanhållning. Du får friheten att bygga din egen verksamhetsdel och skapa ditt eget team, vilket ger dig en unik möjlighet att forma och driva din karriär framåt.
Ansökan
Skicka din ansökan med CV och personligt brev senast den 13:e april. Urvalet sker löpande. Vi ser fram emot att välkomna vår nya kollega till QRIOS Life Science!
Om företaget
QRIOS Life Science är ett ledande konsultföretag som specialiserar sig på att leverera högkvalitativa lösningar och expertis inom Life Science-sektorn. Vi arbetar nära våra kunder för att förstå deras unika behov och leverera skräddarsydda lösningar som driver innovation och framgång. Med ett starkt fokus på kvalitet och engagemang strävar vi efter att vara den främsta partnern inom vår bransch. Vi är ett konsultföretag som inte är som många andra, inspirerade av de som aldrig slutar leta efter nya lösningar. Som vi säger, QRIOS MINDS GÅR LÄNGRE! Visa mindre

Are you an experienced hands-on in vitro biologist with excellent in vitro experimental skills? Would you like to apply your expertise in a company that follows the science and turns ideas into life changing medicines? Then this role might be the one for you!

QRIOS now offer an exciting opportunity for a dedicated Senior Scientist consultant to join the Bioscience Renal in vitro team within the Early Cardiovascular, Renal and Metabolism (CVRM) therapeutic area. The position is placed at AstraZeneca’s dynamic R&D site in Gothenburg, Sweden.

About the position
As Senior Scientist at the Bioscience Renal department you will be part of a vibrant team that focus on finding new treatment options to patients with renal disease. In the in vitro team we work with various pre-clinical models and different drug modalities. You will take part of both establishing new methods, using a wide array of established analysis in cell culture and advanced 3D models as well as driving new targets. At AstraZeneca, you will work together with experts from different functions and be part of project teams.

Responsibilities
As a senior research scientist in the Renal in vitro team, you will independently design, plan and perform high quality in vitro experiments. You will identify and implement new methods/assays relevant for renal disease area and use a wide array of the latest technologies to analyze biological samples.

• Performing conceptual interpretation and presentation of generated data
• Delivering data, reports, and regulatory documents
Essential for the role
* Master degree in biology, biotechnology, biomedicine, physiology, or medicine
• Flow cytometry knowledge
• Experience from in vitro work in molecular biology and other technologies such as western blot, ELISA and cell imaging
• Extensive expertise in cell culture related work
• Strong oral and written communication skills. English is essential, Swedish is appreciated but is not a requirement

Your profile
Essential for the role:

• Master’s degree in biology, biotechnology, biomedicine, physiology, or medicine
• Experience from in vitro work in molecular biology and other technologies such as western blot, ELISA, flow cytometry and cell imaging
• Extensive expertise in cell culture-related work
• Strong oral and written communication skills. English is essential, Swedish is appreciated but is not a requirement

Desirable for the role:

• PhD in biology, biotechnology, biomedicine, physiology, or medicine
• Proven publication record
• Renal biology background
• Experience from Pharmaceutical industry
• Experience in cell metabolism and mitochondrial biology

About the organisation
This is a consultant assignement at AstraZeneca Göteborg for 1 year starting in May 2025. 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

QRIOS are now looking for an Assoc. Princ. Scientist Bioscience with knowledge of in vivo experimental biology to join the Bioscience Renal in vivo team within the Early Cardiovascular, Renal and Metabolism (CVRM) therapeutic area. This is a consultant assignment at AstraZeneca’s dynamic R&D site in Gothenburg, Sweden.


About the position
As Assoc. Princ. Scientist with the Bioscience department at AstraZeneca you will be part of a vibrant team that focus on finding new treatment options to patients with renal disease. In the in vivo team we work with various pre-clinical models and different drug modalities. You will take part in in vivo deliveries to drive the renal pipeline. At AstraZeneca you will work together with experts from different functions and be part of project teams.

Responsibilities
• Independently design, plan and perform high quality in vivo experiments in preclinical models of renal disease
• Identify and implement new models/assays relevant for renal disease area
• Analyse fluids for biomarker quantification
• Perform conceptual interpretation and presentation of generated data
• Act as Bioscience representative in assigned projects
• Potentially act as new Target Champion, ie proactively identify and develop new target ideas into projects
• Deliver data, presentations, reports and regulatory documents
• Show scientific leadership in areas associated with the role – renal pathology and pathophysiology – by presenting data internally in key forums
• Ensure that own work and work with others is performed according with appropriate safety, health and environment (SHE), qualify and compliance standards, e.g. General Laboratory Standard (GLS)

Your profile
Essential for the role:

• PhD in biology, physiology, pathology or medicine or other relevant areas
• Extensive hands-on experience in running in vivo experiments in rodents with experience in renal models
• Educated and certified for in vivo experimentation
• Proven publication record
• Strong oral and written communication skills. English is essential, Swedish is appreciated but is not a requirement

Desirable for the role:

• Flexibility & independence
• Experience working with preclinical contract research organizations
• Expertise in renal physiology and/or pathology
• Experience from Pharmaceutical industry

About the organisation
This is a consultant assignement at AstraZeneca Göteborg for 1 year starting in May 2025. 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 expertise within in vitro cardiovascular biology and enjoy working in the lab? Would you like to apply your expertise in a global company that is accelerating innovative science and turn ideas into life changing medicines? Join us to discover future treatment of Cardiovascular, Renal and Metabolic diseases!

At AstraZeneca, we work at the cutting edge of science to develop the ground-breaking medicines of the future – here we do things that have never been done before. We put patients first and strive to meet their unmet needs worldwide.

About the position
CVRM is one of three main therapeutic research areas within AstraZeneca. Early CVRM has a patient-centric approach for discovering novel treatments for patients with cardiovascular-, chronic kidney- and metabolic disease and delivers candidate drugs into late-stage clinical development. In the Bioscience Cardiovascular department, we focus on identifying and validating new drug targets for treatment of patients with cardiovascular disease and heart failure, as well as evaluating pharmacological aspects, e.g. efficacy and mechanism of action, of potential new drug candidates. The in vitro team delivers key data to projects across all phases of the drug discovery and development process, and we work with different modalities such as small molecules, modified mRNA, antibodies, cell therapy, antisense oligonucleotides and peptides.

We are now recruiting a Senior Scientist with expertise in cardiovascular biology to join the Bioscience Cardiovascular in vitro team within the Cardiovascular, Renal and Metabolism (CVRM) therapeutic area at AstraZeneca in Gothenburg, Sweden.

Responsibilities
As a Senior Scientist you will play a key role in driving science and projects within the cardiovascular area forward. This is a lab-based role where you will explore novel drug targets with key in vitro data. Collaboration is critical for successful delivery of drug projects, and you will work closely with scientists/teams from a wide range of different functions within AstraZeneca as well as with external partners and collaborators. You will work with in vitro biology using cell lines, pluripotent stem cells (PSC) and primary cardiovascular cells along with molecular and functional biology techniques. You will have the opportunity to try novel techniques and ideas required for progressing existing portfolio and novel science. Responsibilities include:

- Independently design, develop and run in vitro studies and assays for target identification and validation
- Work with molecular biology methods, imaging and assays for functional readouts such as contractility and cardiac metabolism
- Contribute to communications of scientific findings through publications in scientific journals and at meetings
- Proactively contribute to a vibrant and innovative working environment where improvements and new ideas are adopted and freely shared

Your profile
Essential for the role:

• PhD or master’s degree in biology, pharmacology, cardiovascular disease or similar
• Strong experience in cell and molecular biology, biochemistry and relevant in vitro/ex vivo assays within the cardiovascular area
• Experience in handling and manipulating relevant PSC cells and primary human and animal cardiac cell types, including cardiomyocytes
• Excellent English communication skills, both spoken and in writing

Desirable for the role:

• Experience with cardiomyocyte biology and function in healthy and diseased systems
• Background in drug discovery and development in the pharmaceutical industry
• Background in Vivo and in Vitro

About the organisation
This is a consultant assignement at AstraZeneca Göteborg for 1 year starting in April 2025. 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

Gillar du analytisk kemi, är kvalitetsfokuserad, engagerad och sätter säkerheten först? Gillar du att jobba självständigt, i team och tvärfunktionellt samt ständigt jobba med förbättringsarbete? Då kan du vara den vi söker!
Just nu har jag ett uppdrag hos kund i 3 månader med god chans till förlängning.

Om tjänsten
Är du en erfaren laboratorieingenjör som vill arbeta inom kemiindustrin i Göteborg? Tjänsten innebär att du kommer att utföra rutinarbete på lab, där du kommer att få användning av både dina praktiska och teoretiska kemikunskaper.
Har du i en tidigare roll arbetat med GC/ HPLC och vattenanalyser ses detta som meriterande.

Dina arbetsuppgifter i huvudsak
• Genomföra rutinmässiga analyser med olika analysmetoder effektivt och säkert
• Utföra vatten- och miljöanalyser med bland annat GC, HPLC, AA, X-ray, ICP, Karl Fischer
• Utföra viktiga analyser för produktionsavdelningen och kunder i Sverige
• Rapportering av analysresultat i systemet LIMS
• Kvalitetsarbete som tex. kalibrering och underhåll

Vem är du?
• Har en eftergymnasial utbildning med inriktning mot kemiteknik.
• Erfarenhet av tidigare laboratoriearbete. T.ex. som laboratorietekniker, laboratorieassistent eller annan närliggande roll.
• Meriterande om du har erfarenhet av att ha arbetat med GC, HPLC och/eller ICP.
• Du behöver behärska det svenska språket i både tal och skrift.

Vidare har du en god planerings- och prioriteringsförmåga, samt kan arbeta självständigt och strukturerat. I rollen som laboratorieingenjör behöver du vara kreativ, noggrann samt värdesätta kvalitet och stolthet i det du levererar. Du har lätt för att samarbeta och gillar att se praktiska lösningar på olika problem. Du förväntas vara en del av, och bidra till löpande förbättring och effektivisering av arbete på lab. Därför ser vi att du behöver trivas i en föränderlig miljö, då arbetsmiljön kräver ett aktivt HSM-arbete (hälsa, säkerhet, miljö) ser vi också att du är en ansvarsfull person, som har stor förståelse för detta i det dagliga arbetet.

Om verksamheten
Detta är konsultuppdrag inom kemiindustrin i Göteborg under 3 månader med god chans till förlängning. Under uppdragets längd kommer du att vara anställd av QRIOS. QRIOS kan erbjuda flera möjligheter till dig som har en biokemisk, kemiteknisk eller naturvetenskaplig bakgrund. Vi arbetar med de främsta av Sveriges läkemedels- och life scienceföretag. Så, vare sig du är intresserad av forskning, Regulatory Affairs, Quality Assurance, miljö- och kvalitetskontroll, marknad och försäljning eller bara önskar ett karriärbyte, har vi en tjänst för dig.


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

Har du erfarenhet av att leda människor inom processindustrin, kunskap inom roterande utrustning och är redo för nästa utmaning i arbetslivet? Då kan detta vara möjligheten för dig! Vi söker nu en chef till vår roterande avdelning på St1 Refinery AB.
OM TJÄNSTEN
Som chef för roterande avdelningen har du det övergripande ansvaret för vår roterande utrustning. Tjänsten ingår i underhållsavdelningen och du rapporterar direkt till vår Underhållschef. I arbetsuppgifterna ingår att budgetera, planera och samordna, både förebyggande och avhjälpande underhåll. På avdelningen arbetar en underhållsingenjör, en koordinator samt tio tekniker.
Huvudsakliga ansvarsområden/arbetsuppgifter:

Ta fram årlig budget


Leda arbetet med tillförlitligheten av vår roterande utrustning samt tillse att vår reservdelshållning är anpassad till utrustningens behov


Tillsammans med driftavdelningen och övriga delar av underhåll prioritera och besluta omfattning av reparationer och underhåll


Vara beställare och projektledare av projekt inom ansvarsområdet


Tillse att arbetet genomförs enligt lagar och rutiner med avseende på hälsa, säkerhet, miljö och kvalitet


Följa upp arbetet med avseende på dokumentation och ekonomi


Beredskapstjänst förekommer


DIN PROFIL

Erfarenhet från drift och / eller underhåll inom processindustri och med roterande utrustning ser vi som klart meriterande


Minst 5 års erfarenhet från arbete som chef inom processindustri


Teknisk högskoleutbildning med inriktning mot maskinteknik är meriterande


God kännedom om Microsoft Office


Vi söker dig som gillar att ta eget ansvar och egna initiativ samt trivs att jobba i en organisation med korta beslutsvägar och möjlighet att påverka. Då arbetet präglas av samarbete och interaktion med både interna och externa kollegor förutsätter vi att du har gott ordningssinne, samarbetsförmåga och kan uttrycka dig väl på både svenska och engelska. Du behöver också tycka det är roligt att arbeta i en bransch som befinner sig mitt i en förändringsresa. Viktigt för rollen är att du tycker om att leda och är intresserad av människor och deras utveckling. Att arbeta inom processindustrin ställer också höga krav på skyddsmedvetenhet och därför ser vi också att du är en ansvarsfull person som alltid strävar efter att förbättra din och dina kollegors arbetsmiljö.
Vår personal är viktig för oss och har många förmåner som uppskattas bland våra anställda. Förutom kompetenta och engagerade kollegor så erbjuder vi ett intressant och spännande arbete med stora kontaktytor samt en en platt organisation där kommunikations- och beslutsvägar är korta. Övriga förmåner inkluderar:

Attraktiv bonus utöver din grundlön


Utfyllnad av föräldraförsäkring vid barnledighet


ATK (arbetstidsförkortning)


Andel i företagets vinstandelsstiftelse


Goda träningsmöjligheter på siten med ett nyrenoverat stort gym, uppvärmd pool och idrottshall


Friskvårdsbidrag


Subventionerad företagshälsovård


Subventionerad lunchförmån


Subventionerade aktiviteter där vi hittar på roliga saker tillsammans


Henrik Teiffel, Underhållschef:
”Jag upplever att på St1 Refinery känner man sig alltid välkommen och det är alltid trevligt att komma till jobbet! Hos oss på underhållsavdelningen så finns det en nyfikenhet och öppet sinne för förändringar hos medarbetarna. Ställs vi inför utmaningar så hjälper vi varandra för att tillsammans arbeta lösningsfokuserat.
I rollen som chef roterande är det viktigt att vilja utveckla struktur och arbetssätt för att skapa ständiga förbättringar”
OM St1
Vi är ett nordiskt energibolag som vill vara med och driva energiomställningen och vår vision är att bli den ledande producenten och säljaren av CO?-medveten energi. För verksamheten i Sverige följer vi Sveriges klimatmål vilket innebär att vi senast 2045 ska ha nettonoll utsläpp. På vårt raffinaderi i Göteborg har vi ungefär 280 anställda med experter och specialister inom processindustrin med produktion och underhåll av anläggningen. Raffinaderiet är verksamt dygnet runt, året runt. Raffinaderiet är sedan 1997 miljöcertifierat enligt EMAS och ISO 14001. Vi investerar stort i biogas och driver också två stora projekt för att tillverka avancerade biodrivmedel respektive elektrobränslen för flyget. Vi startade vår första gröna anläggning nyligen som producerar biodiesel och vi håller också på att anlägga en solcellspark i Göteborg. 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
Responsibilities for the role:

• 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

Desirable in the role:

• Experience from working with liquid handlers
• Experience with LC software (MassHunter, Chemstation, Masslynx, Virscidian, etc...).
• Knowledge of pharmaceutical drug discovery
• Proficiency with other analytical techniques such as NMR, IR & MS.
• Basic knowledge of synthetic chemistry.

About the organisation
This is a consultant assignement for six months at AstraZeneca in Gothenburg. Start day in March 2025.
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
Do you have strong experience in cell culture and you would like to apply your expertise in a company that is accelerating innovative science and turn ideas into life changing medicines? Join our Microphysiological systems (MPS) team to discover future preclinical models that can support development of new medications for Cardiovascular, Renal and Metabolic diseases!

At AstraZeneca, we are harnessing advanced cell models, microfluidic chip technologies, multi-omics screens, and mathematical modelling to help us achieve the next wave of breakthroughs – here we do things that have never been done before. Are you excited to contribute, then you might be the person we are looking for!

This role will be based in the MPS team at the Early Cardiovascular, Renal and Metabolism (CVRM) department in our dynamic R&D site in Gothenburg, Sweden. The MPS team establishes and applies state-of-the-art MPS platforms to support the CVRM portfolio with emerging therapeutic area needs and new drug modalities. Our mission is to improve translatability from in vitro models to humans and accelerate drug discovery and development.

Responsibilities
You will execute and provide input into the practical delivery of MPS studies and support the development, characterization, and optimization of new models.

Responsibilities include:

• Take part in the design, conduct, interpretation and reporting of studies with advanced cell models and MPS.
• Carry out various downstream analyses from the cell culture samples with versatile in-vitro analytical methods such as, but not limited to, ELISA’s, qPCR, staining and imaging.
• Join further model development activities to support drug projects with MPS data for resolving mechanisms of action, target identification, and candidate drug evaluation.
• Effectively communicate and collaborate across the Early CVRM and with the key stakeholders in other functions.

Your profile
Essential for the role:

• Master’s degree + 2 years of relevant experience.
• Background in Pharmacy, Biology, Biotechnology, Biochemistry, Medical Biosciences, Bioengineering or similar
• Strong hands-on cell culture experience
• Experience with primary cells or hPSCs
• Versatile in-vitro analytical methods (e.g., qPCR, staining and high-content imaging, plate-based assays e.g., ELISAs)
• Independent study design, laboratory work, and data analysis
• Data visualization and statistical analysis
• Excellent interpersonal skills and excellent communication skills in English, both verbal and in writing
• Strong ability to engage and collaborate across boundaries with a problem-solving attitude and focus on delivery

Desired for the role:

• Experience in 3D cell culture, i.e., spheroids, organoids, or multicellular co-cultures
• Experience with one or more of cell models for liver, kidney, cardiac, pancreas, or adipose tissue
• Experience in culturing immune cells
• Handling microfluidic chips
• RNA-Seq and proteomics
• Workflow automation e.g. robotic liquid handling
• Experience from the pharmaceutical industry

About the organisation
This is a consultant assignment at AstraZeneca in Göteborg for 1 year, starting in April 2025.
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 experience in flow cytometry and versatile knowledge in cell culture, and are you eager to apply your expertise in a company that accelerates innovative science to turn ideas into life-changing medicines? Join our Microphysiological Systems (MPS) team and contribute to the discovery of future preclinical models that support the development of new medications for Cardiovascular, Renal, and Metabolic (CVRM) diseases!

About the position
At AstraZeneca, we are harnessing advanced cell models, microfluidic chip technologies, multi-omics screens, flow cytometry, and mathematical modelling to achieve the next wave of breakthroughs – here we do things that have never been done before. Are you excited to contribute? Then you might be the person we are looking for!

This role is based in the MPS team at the Early CVRM department in our dynamic R&D site in Gothenburg, Sweden. The MPS team establishes and applies state-of-the-art MPS platforms to support the CVRM portfolio with emerging therapeutic area needs and new drug modalities. Our mission is to improve translatability from in vitro models to humans and accelerate drug discovery and development.

Responsibilities
You will execute and provide input into the practical delivery of MPS studies while also serving as a flow cytometry (FACS) scientist. You will support the development, characterisation, and optimisation of advanced cell models and flow cytometry-based assays. We’ll look to you as an expert in cell and molecular biology techniques, and you will independently carry out various downstream in-vitro analytical methods.

Responsibilities include:

• Develop and execute flow cytometry-based assays for cell characterisation and functional analysis including panel design.
• Take part in the design, conduct, interpretation, and reporting of studies with advanced cell models and MPS.
• Carry out various downstream analyses from cell culture samples with versatile in-vitro analytical methods such as, but not limited to, ELISA, qPCR, staining, and imaging.
• Join further model development activities to support drug projects with MPS and flow cytometry data for resolving mechanisms of action, target identification, and candidate drug evaluation.
• Effectively communicate and collaborate across the Early CVRM department and with key stakeholders in other functions.

Your profile
Essential for the role:

• Master’s degree + 4 years of relevant experience.
• Background in Pharmacy, Biology, Biotechnology, Biochemistry, Medical Biosciences, Bioengineering, or similar.
• Proficiency in flow cytometry, including assay development, troubleshooting, and data interpretation.
• Strong hands-on cell culture experience.
• Versatile in-vitro analytical methods (e.g., qPCR, staining and high-content imaging, plate-based assays such as ELISAs).
• Independent study design, laboratory work, and data analysis.
• Data visualization and statistical analysis.
• Strong interpersonal and communication skills in English, both verbal and written.
• Strong ability to engage and collaborate across boundaries with a problem-solving attitude and focus on delivery.

Desired for the role:

• Experience in 3D cell culture, i.e., spheroids, organoids, or multicellular co-cultures.
• Experience with one or more of the following cell models: liver, kidney, cardiac, pancreas, or adipose tissue.
• Experience in culturing immune cells.
• Handling microfluidic chips.
• Workflow automation, e.g., robotic liquid handling.
• Experience from the pharmaceutical industry.

About the organisation
This is a consultant assignment at AstraZeneca in Göteborg for 1 year, starting in April 2025.
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 a background in Molecular and/or cell biology, aren’t afraid of trying new paths and doing things differently? Do you also feel passionate about the possibilities of science to change lives? Perfect, your next challenge might be this role at a company within Life Science in Gothenburg.

A position has arisen for a highly motivated Scientist – Molecular and Cell Biology to join as a consultant for 3-6 months. We are looking for a candidate who will be working in the lab and providing dedicated experimental support.
The company is working within the area of regenerative medicine and creating tissue-based solutions.

Your profile
Essential Requirements:
• BSc/MSc/PhD degree in Molecular Biology, Biomedical, or a related discipline with significant practical experience.
• Extensive experience in molecular and cellular biology techniques including protein and gene expression analysis, Western Blot, qPCR and cell culture. Ideally applied to relevant cellular assays and in vivo samples.
• Excellent communication skills and an ability to operate in a multi-disciplinary research environment.
• Independent analysis and evaluation of complex data and delivery of data to agreed timelines.

You have good social and communication skills, is collaborative and a great team player. You should also be able to work independently and have a positive, goal oriented and problem-solving attitude. Excellent English is required, both spoken and written.

About the organisation
This position is a consultant assignment at a company within Life Science in Gothenburg for 3-6 months. This assignment can be prolonged. 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

Pharmaceutical Technology and Development (PT&D) is the organization that turns brilliant science into actual medicines that help millions of people. We work across the entire value chain, designing and delivering active ingredients, formulations and devices for new medicines and providing expert technical support to all AstraZeneca’s commercial drug substances and products to ensure we successfully supply medicines to patients.
Drug Product Delivery (DPD) within PT&D 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, agility and teamwork enable us to deliver high value to clinical trials.

We are now looking for one Associate Scientists/Operational Technologists starting as soon as possible with the location Gothenburg, Sweden.

Responsibilities
You will have a great opportunity to learn more about pharmaceutical development working with experienced operators. This role contributes to the packaging of drug products in development phase for clinical studies. All below activities will have an impact on the speed, quality and cost of the AZ development portfolio.
Practical hands-on work in our Good Manufacturing Practice (GMP) facilities with dedicated tasks in close collaboration and to support DPD Scientist/Senior Scientist e.g. assisting GMP operators with:
-Preparation of process rooms and equipment before and after clinical manufacture
-Assembly/disassembly and cleaning of equipment
-Primary packing, i.e. packing of tablets/capsules in bottles (manually or automated)
-Secondary packing, i.e. labelling of study material (manually or automated)
-Working according to SHE (Safety Health and environment) and GMP standards

The role is intended to be used in a flexible way to resolve short term bottle necks. The role holder will not become fully qualified as a GMP operator but will be able to carry out much of the work expected from operators under supervision.

Your profile
Preferred experience/requirements
- You must have completed your studies at upper secondary school level e.g. in natural/technical sciences
-It is essential that you follow written procedures carefully and document executed tasks.
-GMP knowledge is desirable
-Interest in technique and manufacturing equipment and practical hands-on work is desirable
-You need to be flexible with good team working skills.
-Good knowledge of oral and written English is a requirement

About the organisation
This is a consultant assignment for 6 months at AstraZeneca in Gotenburg.
During this time you will be hired by QRIOS.
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 expertise in regulatory and overall understanding of GxP requirements? Are you highly collaborative and like contributing to clear instructions and implementing process improvements? This opportunity as Processes Specialist in the Regulatory Process and Compliance team might be the right opportunity for you.

At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means putting patients first, doing the right thing and working together to make the impossible a reality. If you are swift to action, willing to collaborate, and curious about what science can do, then you’re our kind of person.

Responsibilities
As a Processes Specialist in the Regulatory Process and Compliance team you will be working with the Process team members and taking responsibility for the management of assigned tasks related to procedural document management. You will act as technical writer and reviewer, and support project management to ongoing procedural document update program.
You will be accountable to execute the delivery of the authoring and lifecycle management of current procedural documents. We hope that you have the drive to establish a culture of continuous improvement, high performance, flexibility and quality, emphasizing a “can do” attitude and ensuring high standards of quality in all outputs.

Other key responsibilities in this position:
• Identify opportunities for and drives the enhancement of existing processes and procedural documents
• Using understanding of regulatory processes and regulations to provide support to regulatory process team
• Identify opportunities to improve and simplify the methodology in processes and guidance, provide practical solutions
• Review and verify documents and data for accuracy and completeness
• Collaborate with team members to ensure high standards of quality in all outputs
• Contribute to communication and change management activities associated with process initiatives

Your profile
Essential for the role:
• A science/pharmacy/nursing degree, with relevant experience (pharmaceutical, regulatory, safety)
• Exceptional attention to detail and accuracy
• Excellent written and verbal communication skills in English
• Knowledge of the drug development process and sufficient knowledge to understand aspects of Regulatory
• Experience in working cross-functionally
• Proven ability to work across cultures

Desirable for the role:
• MSC/PhD in scientific discipline
• Knowledge of regulatory expectations and regulations
• Knowledge of existing AstraZeneca organisation
• Experience of working in a global organisation, preferably within the pharmaceuticals industry, and of the drug development life cycle

About the organisation
This is a consultant assignment at AstraZeneca in Göteborg from January 2025 until end of August 2025. 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

Vi har möjligheten att tillsätta 2 konsulter till ett av världens mest energieffektiva raffinaderier!
St1 i Göteborg behöver förstärkning på lab, med olika uppdragslängd.
Det ena uppdraget är 3-6 månader och det andra är 12 månader.

Om tjänsten
Är du en erfaren laboratorieingenjör som vill dela St1 vision om att vara den ledande producenten och försäljaren av CO2-medveten energi? Vi söker nu två drivna och engagerad laboratorieingenjörer som vill ha en ansvarstagande roll i ett ledande energiföretag i Göteborg. Tjänsten innebär att du kommer att utföra rutinarbete på lab, där du kommer att få användning av både dina praktiska och teoretiska kemikunskaper.
Har du i en tidigare roll arbetat med GC/ HPLC, ses detta som meriterande.

Dina arbetsuppgifter i huvudsak
• Genomföra rutinmässiga analyser med olika analysmetoder effektivt och säkert
• Utföra bränsle- och vattenanalyser i laboratorium utrustat med bland annat GC, HPLC, AA, X-ray, ICP samt speciell instrumentering för att kunna utföra petroleum-och miljöanalyser
• Utföra viktiga analyser för både produktionsavdelningen och depåer runt om i Sverige
• Rapportering av analysresultat i systemet LIMS
• Kvalitetsarbete som tex. kalibrering och underhåll

Vem är du?
• Har en eftergymnasial utbildning med inriktning mot kemiteknik.
• Erfarenhet av tidigare laboratoriearbete. T.ex. som laboratorietekniker, laboratorieassistent eller annan närliggande roll.
• Meriterande om du har erfarenhet av att ha arbetat med GC, HPLC och/eller ICP.
• Du behöver behärska det svenska språket i både tal och skrift.

Vidare har du en god planerings- och prioriteringsförmåga, samt kan arbeta självständigt och strukturerat. I rollen som laboratorieingenjör behöver du vara kreativ, noggrann samt värdesätta kvalitet och stolthet i det du levererar. Du har lätt för att samarbeta och gillar att se praktiska lösningar på olika problem. Du förväntas vara en del av, och bidra till löpande förbättring och effektivisering av arbete på lab. Därför ser vi att du behöver trivas i en föränderlig miljö, då arbetsmiljön kräver ett aktivt HSM-arbete (hälsa, säkerhet, miljö) ser vi också att du är en ansvarsfull person, som har stor förståelse för detta i det dagliga arbetet.

Om verksamheten
Detta är konsultuppdrag med snarast start på St1 i Göteborg. Under uppdragets längd kommer du att vara anställd av QRIOS. QRIOS kan erbjuda flera möjligheter till dig som har en biokemisk, kemiteknisk eller naturvetenskaplig bakgrund. Vi arbetar med de främsta av Sveriges läkemedels- och life scienceföretag. Så, vare sig du är intresserad av forskning, Regulatory Affairs, Quality Assurance, miljö- och kvalitetskontroll, marknad och försäljning eller bara önskar ett karriärbyte, har vi en tjänst för dig.

I detta konsultuppdrag är St1 vår kund och nedan kan du läsa deras företagsbeskrivning:
Inom företaget pågår ett spännande utvecklingsarbete, och St1 erbjuder dig ett utmanande, omväxlande och inspirerande arbete. Du kommer att arbeta i ett företag där din insats syns och påverkar, i en miljö där du blir en viktig del av teamet. På St1 har vi en engagerande kultur av entreprenörskap och innovation.
Läs mer på följande länk:
https://career.masterhelp.se/st1-refinery


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

Är du den framtida ledare som vi söker för att växa och utveckla vår affär inom Life Science?
QRIOS Life Science söker nu en driven och engagerad Business Unit Manager med passion för att skapa tillväxt och utveckling inom vår verksamhet. Om du är en konsultchef med hög energi, drivs av affärer, rekrytering och ledarskap, och har ett intresse av strategier och verksamhetsutveckling, är detta chansen för dig att ta nästa steg i karriären!
QRIOS är ett värderingsdrivet bolag där våra värderingar, Passion & Execution, står för mer än bara ord. De påverkar vad vi gör och hur vi driver bolaget. Som ett värderingsdrivet bolag ger vi oss möjligheten att särskilja oss och skapa en unik förutsättning när det gäller att bygga ett bolag drivet av våra handlingar och beteende. Det är vi tillsammans som bygger kultur och värdegrund, inifrån och ut.
Om tjänsten
Som Business Unit Manager kommer du att ha en central roll i vår organisation, där du ansvarar för att driva vår B2B-försäljning av konsulter, utveckla strategiska kundrelationer, samt coacha och utveckla befintligt team och säkerställa lönsamhet inom ditt affärsområde. Du kommer att ha stor frihet att utveckla enheten och din affär, samtidigt som ditt ansvar som ledare ökar i takt med att bolaget växer.
Dina ansvarsområden

Försäljning av konsulter: Driva och utveckla försäljningen av våra konsulttjänster inom Life Science-sektorn.


Rekrytering och kundbearbetning: Ansvar för rekryteringsprocesser samt strategisk bearbetning och att vårda kundrelationer.


Ledarskap: Motivera och leda ditt team mot uppsatta mål, och säkerställa att både medarbetare och kunder är nöjda.


Affärsutveckling: Identifiera nya affärsmöjligheter och utveckla strategier för att expandera vår marknadsnärvaro.


Team Building: Bygga upp din verksamhetsdel från grunden och skapa ditt eget team.


P&L-ansvar för enheten.


Profilen vi söker har

Minst 3 års erfarenhet av B2B-försäljning av konsulter inom Life Science, med dokumenterad framgång inom området.


Erfarenhet av rekrytering och strategisk kundbearbetning.


Erfarenhet av ansvar för P&L. 


Relevant akademisk utbildning, gärna inom teknik eller naturvetenskap.


Flytande svenska och engelska, både i tal och skrift.


Som person är du inspirerande, har hög energi och är handlingskraftig. En förutsättning för att lyckas i rollen är att du har ett stort intresse för människor och teknik. Du är driven och visar vägen framåt för dina medarbetare genom att sätta upp tydliga mål och coacha dem i rätt riktning. Vidare är du inlyssnande och omtänksam och arbetar utifrån våra värderingar. Att både sälja och leda är en självklarhet för dig.
Vi erbjuder en dynamisk och utvecklande arbetsmiljö där du får möjlighet att påverka och forma vår framtid. Hos oss får du en roll med stort eget ansvar och möjligheter till både personlig och professionell utveckling. Vi erbjuder konkurrenskraftiga villkor och förmåner, samt chansen att vara en del av ett engagerat team med hög kompetens och stark sammanhållning. Du får friheten att bygga din egen verksamhetsdel och skapa ditt eget team, vilket ger dig en unik möjlighet att forma och driva din karriär framåt.
Ansökan
Skicka din ansökan med CV och personligt brev senast den 30:e September. Urvalet sker löpande. Vi ser fram emot att välkomna vår nya kollega till QRIOS Life Science!
Om företaget
QRIOS Life Science är ett ledande konsultföretag som specialiserar sig på att leverera högkvalitativa lösningar och expertis inom Life Science-sektorn. Vi arbetar nära våra kunder för att förstå deras unika behov och leverera skräddarsydda lösningar som driver innovation och framgång. Med ett starkt fokus på kvalitet och engagemang strävar vi efter att vara den främsta partnern inom vår bransch. Vi är ett konsultföretag som inte är som många andra, inspirerade av de som aldrig slutar leta efter nya lösningar. Som vi säger, QRIOS MINDS GÅR LÄNGRE! Visa mindre

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 solid-state scientists to join our solid state and automation team within Early Product Development and Manufacturing (EPDM) in Gothenburg.

About the position
ou would join a highly collaborative team and help us deliver the solid-state science to product development within the early portfolio from discovery up into 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.
The successful applicant will become a core member of the global Solid-state skill area which is responsible for ensuring suitable physical form screening, selection and control within drug substance and product. You will get the opportunity to apply your excellent crystallography and solid-state 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 solid-state science at AstraZeneca.

Responsibilities
• Deliver solid state characterisation data in our state of the art laboratory using techniques like TGA, DSC, XRPD and DVS.
• Responsible for ensuring suitable physical form screening, characterisation, form selection and control within drug substance and product.
• Drive solid state skill area in projects and work closely with analytical, formulation, and biopharmaceutics scientists to drive science and innovation.
• Plan and conduct lab-based experimental work in accordance with project timelines.
• Run and develop solid state workflows on automation equipment such as weighting robots and liquid handling systems

Your profile
Essential for the role:

• Master/Bachelor graduate with relevant experience in solid-state chemistry, physical chemistry, or related disciplines.
• Experience in screening and characterization of solids, analytical methodology, and laboratory-based work.
• Experience from conducting solid-state characterization using techniques like TGA, DSC, XRPD, or DVS.

Desirable for the role:

• Interest in lab automation, simulation, or prediction is advantageous.
• Understanding of how physicochemical and solid-state properties affect drug product development.

About the organisation
This is a consultant assignment for 6 months with a chance to extend, starting in January 2025 at AstraZeneca in Göteborg. 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.

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
Are you a scientist with expertise and enthusiasm for applying Surface Plasmon Resonance (SPR) and other biophysical tools to uncover molecular interactions and advance drug discovery? Do you want to leverage your skills to broaden the application of SPR and related techniques in impactful drug discovery projects, while growing your career within a company that values science and transforms ideas into life-changing treatments? AstraZeneca has an exciting opportunity for you!
AstraZeneca is committed to the development of next generation innovative medicines. To help us with this we are looking for a scientist with passion, expertise and experience to join our Protein Science, Structural Biology and Biophysics department as a lab-based Senior Scientist on a one-year contract basis within the Biophysics team. The team is based in our vibrant R&D site in Gothenburg, Sweden and applies biophysical technologies across a range of different modalities to support drug discovery from target validation to drug candidate. You will be part of a team of enthusiastic scientists that deliver deep technical and scientific expertise by applying molecular biophysical methods, including SPR, NMR, ITC, DSF, HDX-MS and single molecule approaches. This is a unique opportunity to contribute to the development and execution of research strategies for the discovery of new medicines – and be focused on the field of Biophysics.

Responsibilities
The role of Senior Scientist is a laboratory-based position supporting the characterization of molecular interactions in drug discovery, with a focus on Surface Plasmon Resonance (SPR) and other biophysical techniques. We are seeking a highly skilled and motivated biophysicist with deep expertise in SPR assay development, method optimization, and screening to join our team on a one-year contract basis. The ideal candidate will have a strong theoretical and practical background in biophysical techniques, particularly SPR, along with experience in protein-ligand interactions. This role is crucial in advancing our research and development projects across various therapeutic areas.

You will have significant control and influence over project direction, allowing you to shape experimental strategies and outcomes. Additionally, you will have opportunities to learn new techniques and develop your leadership skills. Working in a collaborative and innovative environment, you will engage with scientists from diverse disciplines. This position offers a unique chance for professional development in an industrial setting, helping you gain valuable experience and build a strong foundation for future career growth.

You will be responsible for designing and implementing advanced SPR assays, tailored to specific research needs, as well as larger screening activities. You will conduct intricate experiments aimed at understanding binding kinetics, affinity, and thermodynamics, ensuring accurate and precise data collection and reporting. Your expertise will be crucial in analyzing SPR data, interpreting results, and integrating findings with other research data to provide comprehensive insights into drug mechanisms of action. You will collaborate closely with multidisciplinary teams, contributing to the integration of SPR and biophysical findings into broader research objectives. Additionally, you will keep abreast of the latest advancements in SPR and biophysics, continuously applying this knowledge to enhance our research capabilities.

You will document and present your results in both internal and external meetings, playing a vital role in driving our scientific endeavours forward. Finally, to be successful in this role we see that you have good social and communication skills, are collaborative and a strong team player. You should also be able to work independently and have a positive, goal oriented and problem-solving attitude.

Your profile
• Ph.D. or equivalent in Chemistry, Biochemistry, or a related field with a focus on biophysical techniques to characterize molecular interactions, preferably SPR (or something similar system)

• Proficiency with surface-based biosensor platforms (e.g., Biacore, Nicoya, Octet, WAVEsystem) including assay development and optimization.

• Expertise in developing, troubleshooting, and optimizing biosensor assays for high-throughput screening and kinetic data analysis, with proficiency in data analysis software (e.g., Biacore Insight, WAVEcontrol) and protein sample preparation to ensure high-quality samples for biophysical studies.

• Familiarity with complementary biophysical methods such as ITC, MST or DSF as well as protein expression, purification, and characterization techniques to ensure optimal sample quality for biophysical assays.

• Proven reputation gained through an excellent track record of publications and/or conference presentations.

Desirable for the role:

Worked in drug discovery environment.


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
Digital Health, the point at which healthcare, technology, data and analytics converge is an area of great promise with the potential to improve the health of everyone. The Drug Development Data platform team within AstraZeneca has the goal of improving patient experience and outcomes and shortening the time it takes to bring life-changing medicines to patients.

You will be joining R&D IT - an outstanding organization at the forefront of the technology revolution in healthcare. It provides the technology, engineering, data and analytics expertise which delivers the Data Platform underpinning AstraZeneca’s Digital Health strategy and R&D transformation programs. The ambition for this Platform is huge. We are looking for data, technology and change experts to work with R&D IT that will ensure this ambition is met.

Main focus for this assignment is on our CDSIC standard development. Depending on your experience, you may contribute to more strategic planning, quantitative decision making, act as expert in our contact with external providers and collaborators and be a part of the function's adaptation and development of programming tools, standards, and praxis.


Responsibilities
Main focus for this assignment is on our CDSIC standard development. Depending on your experience, you may contribute to more strategic planning, quantitative decision making, act as expert in our contact with external providers and collaborators and be a part of the function's adaptation and development of programming tools, standards, and praxis.



Your profile
- Minimum educational level is a BSc degree in a relevant subject such as statistics, biostatistics, mathematics, computer science, life science or engineering
- Expertise in clinical data standards development, in CDISC and standards development within Pharma industry
- Good collaboration, communication and influencing skills
- Good written and spoken English

Personal Qualities Candidates should possess good social skills, be strong team player and be able to work effectively in a global organization where teams often are geographically dispersed. You should be able to work independently, take own initiatives and have a positive, goal oriented and problem-solving attitude. It is essential to have good organizational and communication skills and you should be able to analyze and summarize your results and be comfortable in presenting them. Successful candidates will have the ability to communicate subject matter expertise to other experts, as well as an interest in the application of programming in pharmaceutical 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. Being a consultant at QRIOS gives you opportunities to try different industries, companies and roles.

It 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. Visa mindre