Lediga jobb Hays AB i Göteborg

Hays is now looking for a consultant to take on the role of Clinical Supply Associate at AstraZeneca in Mölndal for 12 months.

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

At AstraZeneca, we believe in the potential of our people, and you'll develop beyond what you thought possible! We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us.

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

The Clinical Supply Associate (CSA) supports Global Clinical Supply Chain (GCSC) to ensure the delivery of clinical material and associated information to meet the agreed clinical demand. This role is a great opportunity for someone who thrives working in a task based, agile and global environment.

What you'll do
The CSA supports GCSC teams with task-based activities that include:
* Timely management of temperature excursion assessment affecting clinical trial material.
* Coordination of the country release requests of study labelled material.
* Electronic document archiving and quality control.
* User Acceptance Testing of digital systems.
* Support the coordination of the purchase and delivery of External Commercial Products.
* Facilitation of documentation activities ensuring inspection readiness to meet international GMP standards.
* Documentation and coordination of product complaints and GMP deviations.
* Utilising Supply Chain Management systems to support agile ways of working.
* Continually improving the Clinical Supply Chain processes through visual management, problem solving, global standardisation and process confirmation.

In this role you will have the opportunity to develop leadership skills and enterprise acumen, quickly becoming a Super User within a core role and/or leading improvement initiatives. You will work with multiple customers and partners internally and externally across all phases of the drug development lifecycle, covering small and large molecule drug products. You will follow SHE and GMP standards and will be personally accountable for these areas within your own work plans.

So, what's next!
Are you already imagining yourself joining our team? Good, because we can't wait to hear from you. Visa mindre

Research Scientist, Biobank Scientist

Hays Life Science is looking for a new consultant to become a Biobank Scientist at AstraZeneca in Gothenburg, Sweden. This is a one-year consultant assignment with a preferred start on 22nd of April.

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. However, as a company, we are more than one of the world's leading pharmaceutical companies, we are proud to have a unique workplace culture that inspires innovation and collaboration. AstraZeneca employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.

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

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

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

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

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

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

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

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

AstraZeneca is one of the world's most exciting biopharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world. Visa mindre

Analytical Chemists (Scientist or Senior Scientist) - Early Product Development and Manufacturing

Hays Life Science is now looking for a new consultant to become an Analytical Chemist at AstraZeneca in Gothenburg, Sweden. This is a consultant assignment for 8 months.

Analytical Chemists (Scientist or Senior Scientist) - Early Product Development and Manufacturing, AstraZeneca Gothenburg

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

Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) across all the AstraZeneca therapy areas.
Our vision is to be "pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future".
We're looking for talented and motivated analytical chemist to join one of our analytical characterization teams within Early Product Development and Manufacturing (EPDM) in Gothenburg.
You would join a highly collaborative team and together we will deliver the analytical science to product development within the early portfolio up to phase II.
To be successful in this role you will need a strong scientific background with good skills in written and verbal communication and the ability to engage and collaborate across boundaries with a positive problem-solving attitude and delivery focus.
This is a lab-based role where you will work collaboratively with colleagues, documenting your experiments carefully and to the right quality. You will get the opportunity to apply your excellent analytical expertise to the drug projects you are working in, contributing to the progression of these projects and drive the scientific development within the field of analytical science at AstraZeneca.

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

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

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world. Visa mindre

Business Support Coordinator

Hays Life Science is looking for a new consultant to become a Business Support Coordinator at AstraZeneca in Gothenburg, Sweden. The assignment is one year long with a preferred start in the middle of April 2024.

Are you an experienced administrator with a can-do attitude? Do you enjoy working in a dynamic global setting? Do you enjoy interacting with people? Join our team and support the delivery of life-changing medicines for patients! At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality.

Within the Business Support Team in Late-Stage Development Cardiovascular, Renal and Metabolism (CVRM) at AstraZeneca we have a clear vision to be recognized as a global world-class support function that drives business success.

We are now looking for a service minded Business Support Coordinator to join our team in Gothenburg, Sweden.



What You'll do

You will provide PA-support to global leaders in a dynamic and complex business environment. You will also provide global operational support to staff in Late CVRM. Responsibilities will vary from traditional administrative tasks, project coordination, design and preparation of presentation materials, management of SharePoint sites, f2f/virtual meeting facilitation to diary management.



Responsibilities

* Proactive calendar management for senior leaders and line managers including travel arrangements and coordination of meetings in different time-zones. Proactively resolve calendar conflicts, prepare meeting materials and presentations as well as more hands-on meeting support.

* Independently manage the set-up and logistics for meetings, booking meeting rooms, prepare agendas, presentations and take meeting minutes as needed.

* Provide project support for various projects within Late CVRM.

* Set-up and manage documents and materials in Microsoft 365 applications.

* Manage and create purchase orders in Coupa. Travel bookings and expense reports in Concur.

* Resolve complex queries and issues to meet stakeholder and business requirements.



Who we think you are

We believe that you are enthusiastic, highly flexible, open to change, goal-oriented and understand the value of putting customers first. You can self-lead and proactively identify opportunities within our business where you can add value. You have excellent technical skills and excellent knowledge of Microsoft 365. You have experience from PA-support and working in a multicultural global setting. You feel comfortable with multiple priorities and changing agendas. You have a sense of flexibility as no two days are alike.



Essentials for the role

* Excellent interpersonal and communication skills

* Experience of diary management

* Tech-savvy, proficient in Microsoft 365 and virtual meeting technologies

* Resourceful with ability to anticipate needs, manage multiple priorities with tight deadlines.

* Strong self-starter, independent and pro-active with ability to work well in a team environment.

* Relevant administrative experience with senior stakeholders

Desirable for the role

* Relevant professional administration qualification

* Highly skilled expert user of relevant IT-systems

* Good knowledge and skills in graphic design and presentation design

So, what's next?

Do you value giving outstanding service and support to the business and love working in a fast-paced environment? Do you enjoy continuously growing and developing your skills in the areas of administration, support, and project coordination? Are you ready to bring innovative ideas and fresh thinking to the table? Perfect! We have one seat available, and we hope it's yours. Visa mindre

Scientist in vivo, Gut Immunology / AstraZeneca / 9 months / Hays Life Science / Göteborg, Sweden

Hays Life Science is looking for a new consultant to become a Scientist in Vivo Gut Immunology in Gothenburg, Sweden.

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

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

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



Key Duties and Responsibilities

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

This is a mainly lab-based role where you will be involved in ongoing projects focusing on pre-clinical experiments, with the responsibility to design, plan, perform and analyze in vivo studies. Specific focus on mouse models of IBD.



What you'll do

* As a Scientist you will be a vital member of the in vivo community and will contribute to the development and characterization of pre-clinical models of IBD to discover novel therapeutics.

* Under the supervision of the team leader and help from colleagues, you will plan and execute in vivo experiments with rodents.

* You will contribute to the analysis of in vivo studies with a specific focus on FACS analysis.



Essential for the role

* PhD in immunology and understanding of autoimmune diseases with a specific focus on gut immunology.

* Valid education required for compliance to work with live animals in Sweden.

* Several years of hands-on experience with rodents including live animal handling, drug administration through different routes (i.v, i.p., p.o.), blood and organ sampling and processing (colon, small intestine, spleen, lymph nodes).

* At last 5 years of experience with regular FACS analysis of mouse samples (organ processing and digestion, cell staining, antibody panel set up, proficient in the use of BD FACS DIVA machines and Flowjo).

* Ability to organize, execute and interpret the results from in vivo studies according to study plans in agreement with the team leader or other colleagues.

* Experience of maintaining the highest standards of welfare and ethical compliance and ensuring the integrity of the generated data. Familiar with using Good Statistical Practice in animal research and applying the 3R's (reduction, refinement and replacement) across the full range of studies.

* Excellent English written and oral communication skills, including presentation skills.



Desirable for the role:

* Experience with animal models of inflammatory bowel disease (IBD) and in vivo PK/PD relationships.

* Experience with in vivo adoptive cell transfer of T cells (naïve, Treg, CAR T) and subsequent ex vivo analysis.

* Experience with other in vitro methodology in addition to FACS (ELISA/MSD and/or qRT-PCR) to analyze ex vivo samples generated from in vivo studies.



AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world. 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.

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

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

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

Required Skills/ Experience/ Education/ Qualifications:
-Bsc. degree
-Experience in pharmaceuticals, a healthcare related industry or academia/hospital environment related to HBS
-Experience in the review of ICFs regarding use of HBS and knowledge of HBS regulations, laws and standards
-Experience of working with multiple stakeholders while maintaining ethical standards and willingness to challenge inappropriate proposals/actions of senior leaders
-Experience in collection and use of HBS as part of ongoing clinical trials is desirable
-Previous experience as a process owner and process improvement is desirable
-Excellent analytical, written and oral communications skills
-Strong collaborative, partnering, and interpersonal skills
-Strong ability to work independently
-Willingness to take decisions
-Excellent knowledge of English, both written and spoken

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies.
From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world. Visa mindre

Scientist Analytical Chemistry, Inhalation Product Development

Scientist Analytical Chemistry / AstraZeneca / 12 months / Hays Life Science / Gothenburg, Sweden

Hays Life Science is now looking for a new consultant to become the Scientist Analytical Chemistry in Gothenburg, Sweden.

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

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

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

As an Analytical Scientist you will work independently in the laboratory with analytical testing, documentation and also present your data to the project team.

You will join a highly collaborative team who work with both manual and automated analytical techniques to deliver innovative inhaled medicines to patients.

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

Essential for the role:

*Bsc or MSc degree in Analytical Chemistry or other relevant scientific discipline

*Experience from analytical chromatography (UPLC) with relevant detection techniques for small molecules

*Prior experience working as analytical scientist within pharmaceutical industry is desirable

*Experience in aerosol characterization techniques used for inhaled products, such as impactor analysis is desirable

*Experience of working in GMP environment is desirable

*Excellent communication skills and ability to communicate in English both orally and in writing.



Other skills:

Profound knowledge of the discovery and development phase and awareness of clinical drug development.

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world. Visa mindre

Vi söker en erfaren Data Warehouse-utvecklare som vill arbeta på ett marknadsledande företag inom kredithanteringstjänster. Du kommer vara en viktig del av företagets internationella team på över 10 000 medarbetare. Företaget strävar efter att göra skillnad genom att hjälpa både individer och företag att övervinna ekonomiska utmaningar och växa tillsammans. Med företagets globala närvaro öppnas dörrar för dig att utvecklas, specialisera dig och utforska internationella möjligheter

Vad du behöver för att lyckas
Som data warehouse-utvecklare är du medansvarig för att designa, bygga och underhålla företagets data warehouse i Sverige. Du kommer att arbeta nära analytiker och andra delar av verksamheten för att säkerställa att data är strukturerad, korrekt och lättillgänglig. Ditt huvudsakliga fokus kommer bland annat vara att utveckla ETL-processer för att extrahera data från flera källor, omvandla det för att passa företagets datamodell. Andra viktiga uppgifter innefattar att bygga exporter av data till exempelvis klienter. Du kommer också att vara medansvarig för att säkerställa maximal prestanda och skalbarhet.

Viktiga ansvarsområden:

· Designa och utveckla ETL-processer för att extrahera, omvandla och ladda data från olika källor.

· Skapa och underhålla datamodeller, schema och metadata-dokumentation

· Optimera prestanda.

· Övervaka och felsöka problem och fel

· Utveckla och underhålla processer för datamigration och integration

· Hålla dig uppdaterad med branschtrender och bästa praxis inom data warehouse och ETL-utveckling

För att trivas i rollen som Data Warehouse-utvecklare behöver du ha ett stort dataintresse och hög drivkraft. Du bör vara en stark problemlösare med goda analytiska färdigheter. Du kommer att ha möjlighet att både ta eget ansvar och samarbeta i team, och din kommunikationsförmåga kommer vara en värdefull tillgång. Dessutom ser vi gärna till att du har:

· En relevant universitetsexamen inom datavetenskap, informationsteknologi eller relaterade områden

· 5+ år erfarenhet i en liknande roll

· Erfarenhet av ETL-utveckling

· Erfarenhet av server

· Har goda kunskaper i , inklusive query-samt prestandaoptimering

· Har kunskap om datamodelleringskoncept och tekniker

· Tycker om att arbeta med problemlösning och analys

· Goda kommunikationsförmågor, skriftlig och muntlig på svenska och engelska

· Vi förväntar oss att alla våra sökande har en ordnad ekonomi

Avdelningen du kommer att arbeta inom heter Performance Management och är en viktig samarbetspartner med majoriteten av företagets verksamhet och du kommer hjälpa kollegor med allt från automatisering till rapporter och analys.

Företagets värderingar
Du agerar enligt våra värderingar. Våra värderingar är inte ord. De är allt.

Bakom företagets globala expansion och stora digitala transformation ligger fyra enkla men kraftfulla värden: Etik. Hängivenhet. Lösningar. Empati. Det är värderingarna som driver vår vardag, oavsett hur stora vi blir. Andra kanske tycker att de är små saker. Men för oss, är de allt.

Empati, Etik, Hängivenhet, Lösningar - det betyder att du skulle passa bra om du känner igen dig inom följande:

· Du har ett tillväxttänk, med det menar vi: att vi ser möjlighet istället för begränsning.

· Du är inställd på livslångt lärande och positiv till att lära dig nya färdigheter för att hålla dig uppdaterad och alltid se fram emot att förbättra dina prestationer

· Du har god digital kompetens, förstår hur och varför data är en väsentlig del av vår vardag

· Du har en kommersiell medvetenhet, du fokuserar på resultat, med kvalitet och professionalism

· Du är bekväm och frodas av att arbeta i en snabbt föränderlig miljö

· Du har ett inkluderande tänkesätt, du är öppen och flexibel

Vad du behöver göra nu
Om du är intresserad av rollen ansök direkt genom att klicka på "Ansök nu". Vi hanterar ansökningar löpande, så tjänsten kan komma att tillsättas innan sista ansökningsdag som är 2024-01-30 Välkommen in med din ansökan! Visa mindre

Pharmaceutical Material Scientist

Pharmaceutical Material Scientist / AstraZeneca / 10 months / Hays Life Science / Gothenburg, Sweden

Hays Life Science is now looking for a new consultant to become the Pharmaceutical Material Scientist in Gothenburg, Sweden.



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



We now have the opportunity for one consultant to join our team in the role as a Materials Scientist within the Oral Product Development team at AstraZeneca in Gothenburg. The assignment is to end of Dec 2024 on a temporary basis.



Tasks and responsibilities/The role:

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



Essential requirements:

-BSc or MSc typically from pharmaceutics, chemistry or chemical engineering, but also other disciplines with relevant skills.

-Experience from working within the pharmaceutical industry is an advantage.

-Laboratory experience including working with computerized systems.

-Experience of physical characterisation techniques such as laser light scattering (PSD), surface gas adsorption (BET) and powder rheometry (RST/FT4) is desirable.

-Excellent knowledge in written and spoken English is necessary (Swedish is a plus but not mandatory for this position)



Soft skills:

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



AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world. Visa mindre

Pharmaceutical Material Scientist / AstraZeneca Gothenburg / 4 months / Hays Life Science

Hays Life Science is now looking for a Pharmaceutical Material Scientist to join on an assignment at AstraZeneca Gothenburg for 4 months.

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

The arena:

We now have the opportunity for one consultant to join our team in the role as a Materials Scientist within the Oral Product Development team at AstraZeneca in Gothenburg. The assignment is to end of Dec 2023 on a temporary basis.

Tasks and responsibilities/The role:

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

Minimum requirements:

BSc or MSc typically from pharmaceutics, chemistry or chemical engineering, but also other disciplines with relevant skills. Good knowledge in written and spoken Swedish and/or English is necessary as well as laboratory experience including working with computerised systems. If you have experience from working within the pharmaceutical industry, this will be an advantage.

Desirable requirements:

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

Hays Life Science / Procurement Manager / Global pharmaceutical company / Gothenburg, Sweden

Do you have expertise in, and have a passion for procurement? Do you want to be part of a high-performing R&D procurement team that is passionate about delivering real value? Are you ready to join a global pharmaceutical company that has set bold sustainability goals, is data-driven, follows the science, and turns ideas into life-changing medicines? If so, this global pharmaceutical company in Gothenburg, could be the one for you.

Description of the position

This is an exciting opportunity to partner with the R&D units at this global pharmaceutical company to drive their research efforts forward to develop medicines for patients. You will have responsibility for a global spend category at this company (could be single or multiple SET areas). Working with stakeholders, you will develop long-term strategic plans for the entire spend area within the company or region. Manage customer and supplier relationships to ensure that the category strategies are well aligned with current and future business needs and that the supplier base can support these strategies. Monitor the implementation of the category plan to ensure that the supporting process improvement and procurement activities deliver the expected business value in line with the strategic plans.

Key responsibilities

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

Essential experience & skills

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

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

What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Hays Life Science / AstraZeneca / 8 months / Senior Scientist - Immune Cell Therapy / Gothenburg

Senior Scientist - Immune Cell Therapy

Job Description Summary
Fully competent in own research area within Bioscience discipline. Initiate, direct and perform research experiments and implementing strategies. Will be able to work without direct supervision and be able to advise/train less experienced scientists.

Job Description
Are you an experienced scientist in the field of immune cell therapy? Would you like to apply your immunology expertise and turn your ideas into life-changing cell-based medicines for the non-oncology diseases? Join us and be a key player in the build of our new Biopharmaceuticals R&D Cell Therapy department. Together we will push the boundaries of Science!

At AstraZeneca, you will be empowered to be innovative and creative where difference is valued. We thrive in a place where the brightest and most curious minds seamlessly come together in our inclusive environment. The role will be placed at AstraZeneca's dynamic R&D site in the lovely city of Gothenburg, Sweden. Here you will be part of an international, open-minded and creative working atmosphere based on collaboration and innovation.
Biopharmaceuticals R&D is committed to the development of next-generation innovative medicines, and we are building a Cell Therapy Department to establish AstraZeneca as a world leader in Cell Therapy across disease areas within Cardiovascular, Renal and Metabolism (CVRM) and Respiratory and Inflammation (R&I). The Cell Therapy Department will bring together 50 specialists across Europe and the U.S. to support the organisation with cell therapy expertise and capabilities, while working in close collaboration with experts across AstraZeneca globally to leverage the existing and emerging cell platforms, novel cell engineering and gene editing technologies.

What you'll do
Building on your background in immunology you will apply your skills in a regenerative medicine setting, working collaboratively with project leaders, in vitro, and in vivo scientists, and therapy area specialists to ensure efficient progress of Cell Therapy projects. The role is focused on laboratory-based activities and you will use your scientific expertise to design and run experiments and deliver high quality data.
You will play a leading role in developing our scientific capabilities and presenting your work both internally and externally, working in a highly cross disciplinary environment with local and international colleagues.

Accountabilities include:
* Independently assess and report data with little or no guidance, in a clear and concise manner, with an understanding of its implications within the overall context of drug discovery to support project decisions and milestones
* Communicate and share relevant information between distinct projects within the bioscience department as well as across other functions and externally
* Keep up to date with relevant scientific literature and technology platforms as well as writing and publishing scientific papers
* May lead projects and a small team of project researchers.

Essential for the role
In this role it is essential to have good social and communication skills, be collaborative and a strong team player. You should be able to work independently, take own initiatives and have a positive, goal oriented and problem-solving attitude. You also have:
* Ph.D. in Cell Biology, Immunology, or a related discipline, with relevant academic or industrial experience
* Strong background in cell and molecular immunology with experience in CAR-T, Natural Killer or T regulatory cells or other immune cell therapy development
* Extensive experience in culturing and expanding immune cells
* Extensive experience in advanced multi-colour flow cytometry and FACS
* Proficiency in assays interrogating immune cell function, such as cellular activation, cytokine release, proliferation, cytotoxicity/suppression
* Excellent presentation, communication, and organisational skills

Desirable for the role
* Track record of high-quality publications, patents, and/or developing pipeline projects in a pharmaceutical or biotechnology setting
* Experience with gene engineering/editing of primary immune cells including CRISPR/Cas9, viral/ non-viral engineering, base editing, etc.

Why AstraZeneca?
Our Gothenburg site is one of AstraZeneca's three strategic R&D centers. With more than 2,400 employees from over than 50 countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, the history and future of scientific breakthrough come together. We believe that the diversity of our people is crucial to bringing new discoveries to life. Visa mindre

SmartSupplies Inventory Manager Consultant | Gothenburg | Full Time | Hays Life Science



Are you ready to take your career to new heights as a consultant with Hays? We have an exclusive opportunity for an experienced SmartSupplies Inventory Manager Consultant to work on an assignment with our prestigious client, AstraZeneca, at their Gothenburg location.





About AstraZeneca: AstraZeneca is a global, innovation-driven biopharmaceutical business focused on the discovery, development, and commercialization of prescription medicines. They foster a unique workplace culture that inspires innovation and collaboration.



The Role: This is a consultant position through Hays at AstraZeneca. As a SmartSupplies Inventory Manager, you will lead and support initiatives within the Clinical Manufacturing & Supply (CM&S) team, ensuring high quality and adherence to Good Manufacturing Practice (GMP) standards.



Key Responsibilities

* Leading business activities related to external inventory management

* Performing study set up activities in the Smart Supplies system

* Managing updates to item masters, shelf life, and quantities in AZ SmartSupplies

* Developing and providing training in inventory management

* Collaborating across functions to solve problems and improve processes



Essential Requirements

* College/university degree in Science/Engineering

* Track record with managing data changes in GxP systems

* Familiarity with Clinical or Commercial supply chain processes

* Excellent English communication skills Visa mindre

Hays Life Science / Global Study Manager / Gothenburg / AstraZeneca / 12 months

Hays Life Science is now looking for a Global Study Manager for a 12 months assignment at AstraZeneca Gothenburg.

Job details are below and the deadline for CV submission is 15th June.



Global Study Manager

Do you have experience in clinical study management and would like a role where your expertise, as well as your leadership skills, will be highly appreciated? Are you team oriented and do you, as we do, put patients first in your work to make a difference? Then AstraZeneca might be the right place for you to contribute and thrive.

We are recruiting for a Global Study Manager who will join our Study Management Cardiovascular Renal Metabolic Diseases (CVRM) team - which forms part of BioPharmaceuticals Clinical Operations. The position will be based in our vibrant R&D sites in Gothenburg, Sweden.

In the position as Global Study Manager you will support the delivery of global early clinical studies from study set-up through maintenance, close-out and study archiving. It is a role where you work cross-functionally with internal and external partners to lead and deliver aspects of the clinical study according to applicable trial regulations (ex ICH-GCP), AstraZeneca Standard Operating Procedures (SOPs), and in line with AstraZeneca's policies and values.

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

What you'll do:

In the position as Global Study Manager you will play a key role in the study team and work closely with the Global Study Leader to fulfil their accountabilities through coordinating activities that ensures quality, consistency and integration of study data. You will maintain and facilitate interactions with both internal & external functions to provide oversight and ensure efficient study delivery to time, costs and quality objectives, in both internally-run and outsourced studies. The exact accountabilities will differ depending on the exact nature of the clinical program, so a high degree of flexibility is required.

The responsibilities will also include:

* To support the Study leader in project management as per agreed delegation.
* Lead the preparation of delegated study documents (e.g. Informed Consent Form, applicable study plans, etc.), and external service provider-related documents such as specifications, study specific procedures, contracts etc.
* Management of study vendors
* To ensure adequate supply of study materials by liaising with Clinical Supply Chain or external service providers as appropriate.
* Proactively contribute to risk and issue identification, identification of critical to quality factors, development of mitigation and/or action plans for identified risks and issues.
* Adhere to AZ SOPs, global process, applicable Quality & Compliance manual documents and international guidelines (e.g. ICH-GCP) to ensure study is inspection ready at all times.
* Take on assignments on non-drug project work in process improvements and/or leading improvement projects as discussed and agreed upon with their line manager.

To succeed in the role, we also believe that you are team oriented and have ability to prioritize appropriately and manage multiple deliverables. We would like you to have demonstrated leadership skills and hope that you enjoy managing change and actively seek and champion more efficient and effective processes. You work independently and have good communication, collaboration and interpersonal skills.

Essential Requirements:

* Experience working within a global clinical study team and managing third party vendors.
* Experience working with country/regional study teams.
* University degree (or equivalent educational/work experience), preferably in medical or biological sciences or discipline associated with clinical research.
* Experience from pharmaceutical industry and clinical trial experience.
* Good understanding of the drug development process, study management, drug handling and data management as well as deep understanding of ICH-GCP, relevant regulatory/ethics requirements and clinical/drug development.
* Proven organizational, time management and analytical skills; demonstrate very high quality in English, both in written & verbal communication.

Desirable Requirements:

* Knowledge about our therapeutic areas (CVRM)
* Experience from independently leading workstreams within clinical studies Visa mindre

Hays Life Science looking for Formulation Scientist, 12-month at AstraZeneca in Gothenburg

Your new company



* Join Hays Life Science for a 12-month assignment at AstraZeneca, a global, innovation-driven biopharmaceutical business.
* Be part of a company that focuses on the discovery, development, and commercialization of prescription medicines for some of the world's most serious diseases.
* Embrace a unique workplace culture at AstraZeneca that inspires innovation and collaboration, where employees are empowered and rewarded for their ideas and creativity.


Your new role



* You'll join as a Formulation Scientist/Product Developer within the Oral Product Development department at AstraZeneca in Gothenburg.
* Be part of a team generating and evaluating pharmaceutical technologies and formulations.
* Your work will include development, characterization, and documentation, mainly of solid-based formulations, to develop drug products.
* Participate in planning and implementing experiments to generate new formulations and optimize processes at lab and pilot scale.


What you'll need to succeed



* MSc or PhD in chemistry, pharmacy, chemical engineering, food technology or equivalent.
* Good knowledge in written and spoken Swedish and/or English.
* Experience of laboratory work, including working with computerized systems.
* Desirable: Experience from working within the pharmaceutical industry or with manufacturing equipment.
* Desirable: Experience of working in a GMP environment.
* As a person, you should be well organized, analytical, flexible, accurate and have good team working skills.


What you'll get in return



* An opportunity to work with a leading global pharmaceutical company.
* Contribute to meaningful work that helps improve lives worldwide.
* A diverse and inclusive workplace that embraces diversity and equality of opportunity.
* Potential for extension after the initial 12-month period.
* Competitive remuneration.


What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Hays is now looking for a Talent Acquisition Partner for a 1-year contract at AstraZeneca!

Are you an experienced Recruiter ready for an exciting role? Can you envision using your expertise to impact the development of life changing medicines? Then this is an opportunity you don't want to miss!

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

Human Resources (HR) at AstraZeneca is a fast-paced, creative and purposeful environment where ambitious innovative thinking is encouraged. Within HR, they have built a global world class Talent Acquisition function - a team with diverse experience, competence and personalities. They partner with hiring managers and cross-functional specialists throughout the whole recruitment process, and they are passionate about delivering a truly differentiated hiring manager and candidate experience

AstraZeneca are now looking for a new colleague to join its team as Talent Acquisition Partner for a 12 month assignment. AstraZeneca truly believe that everyone contributes with a unique set of competence. Your curiosity and passion for personal development combined with support from colleagues, mentors and leaders, will ensure that you maximise your skills, abilities and contribution.

What you'll do
First and foremost, you will be responsible for managing multiple recruitment processes with local and global top talents. To do this in a successful way, you will partner with hiring managers, HRBPs, business leaders and colleagues.

A typical day includes working with advertising, sourcing, branding, interviewing, candidate discussions, including offers and managing the end-to-end recruitment administration process. Many of their candidates are international talents that relocates to Sweden to join AstraZeneca. The offer process thus includes promoting Sweden as a great place to live, AstraZeneca Gothenburg as a great place to work and their relocation support. In addition to the day-to-day recruitment you may also be working with 3rd party suppliers, supporting projects both locally and globally and mentoring hiring managers. You will be part of a collaborative team where we appreciate and support each other in a high paced and flexible working environment.

Essential for the role
You have a degree in a Science or Human Resources related field, complemented with experience of balancing multiple parallel full life cycle recruitment processes, including the offer process. Your interpersonal skills are excellent and you have a team delivery attitude.

We also believe you have:
* Experience utilizing a range of candidate attraction channels, including LinkedIn
* A creative and innovative approach to utilizing relevant employer branding assets
* Ability to work in a fast-paced, agile and changing environment
* Ability to learn and adopt IT tools and systems
* Demonstrable ability to collaborate across skillsets, personality styles and cultures

Desirable for the role
* Experience of recruiting within Life Sciences, Research & Development, Clinical Operations & Development or Data Science or AI
* Experience of running full life cycle recruitment processes across different countries and skillsets
* Experience of complex recruitments including offering relocation of candidates
* Experience of hiring into Sweden and familiar with basic Swedish employment law.

What to do next
If you are interested in the role, please submit your application with an updated CV now. For specific questions on the role, please contact Greta Kezelyte, [email protected]. Applications will be processed as they come, so don't hesitate to submit your application today.

If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Hays Consultant opportunity as Device Responsible Person and Quality Engineer at AstraZeneca in Gothenburg

About AstraZeneca and the role
AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. At AstraZeneca, we are proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives and are made to feel valued, energized and rewarded for their ideas and creativity.

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

Pharmaceutical 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.

Inhalation Product Development (IPD) in sits within PT&D and is responsible for the development of inhalation products including combinations. Inhalation Product Development delivers the therapies of the future through scientific leadership in drug delivery, formulation and manufacturing the final drug product.
We are looking for a key person to join our multi-functional Product Development Team (PDT) for early phase clinical drug studies (Phase 1-2a). Take this opportunity to work in a role with overall device responsibility for clinical drug delivery system(s) and design control activities.

As part of the PDT this role taker will be device representative on the team and support by performing assessments on the selected drug delivery systems and the drug device combination/combination product. Your knowledge will be highly valued in regular project meetings as the Device specialist; project and clinical supply chain meetings.

What you'll do
Your role will be part Device Responsible Person and Quality Engineer which requires you to conduct the appropriate design controls activities and generate the DHF documentation as prioritized in the design and development.Responsibility to secure that the device and combination product work is delivered with the highest quality and compliant to applicable requirements from Health Authorities, Regulations and Standards where the specific studies will be conducted. Ensure that the right processes, procedures, and standard methodologies are executed and implemented.

Responsibilities will include, but not be limited to:

* Authoring Design Controls documentation including DHF index and ERL/GSPR
* Leading risk assessment activities and ensure that risks process is executed
* Leading Formal Technical and Design reviews
* Performing supplier DHF reviews
* Writing submission text for medical device section
* Supporting Quality with any device issues during clinical studies
* Providing experienced knowledge when it comes to device GXP ways of working
* Being a link between the QA, Regulatory Affairs, Supply Chain and PDT

Essential Requirements:

* Extensive understanding of process for development of Medical Devices and Combination Products; MDD/MDR, ISO 13485, FDA 21 CFR 4 and FDA 21 CFR 820
* Experience in establishing DHFs, Technical Files and Dossiers
* Good understanding technical standards; ISO, IEC FDA guidelines
* Good technical and regulatory writing skills* Proficient in English (speaking and writing)

To succeed in this role, we believe that you have experience of working with development of medical devices within a Medical Device Quality or Regulatory department.We also trust that experience from working in the Pharmaceutical industry is helpful for this role.

Why AstraZeneca
At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We're on an exciting journey to pioneer the future of healthcare.
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.

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

We are looking for an Accountant to a consultant assignment for our client in the automotive industry.

About the company

The company develops and manufactures world-class powertrain solutions for a global market.

With a heritage of more than 100 years of continuous powertrain innovation, their 2,900 employees in Sweden and China works across engine production, R&D and sales.

There are unlimited possibilities at the company for collaborative people who are ready to make the difference.

They are re-imagining motion for a brighter future. Exploring how to push their environmental impact towards zero. Designing tomorrow's powertrain solutions for automotive and beyond. Join them on their journey!


What you'll do

* Basic day to day accounting and more complex accounting questions

* Closing activities

* Take part in process development

* Deliver high quality service and advices within the area of responsibility

* Identify areas for improvement within area of responsibility

* Complex analysis and reporting

* Process management globally

* Measure and follow up the quality and efficiency of global processes, KPI's


Requirements

* University degree in Finance or equivalent

* Around 7 years of experience in Finance or related business

* Good system understanding and efficient data handling

* Sufficient experience and knowledge in the subject area

* Knowledge of Finance processes and policies and full ability of applying these in the daily work

* Experience in executing global processes locally and working effectively in a global team

* Some leadership experience preferred and ability to coach and supervise less experienced

* Fluent in English, oral and written


Assignment details

Location: Gothenburg/Göteborg

Workload: 100%

Remote work: 25%

Start date: 2023-01-01

End date: 2023-06-30, with possibility of extension

Application deadline: 2023-01-01


What you'll get in return

Working as a consultant in Accountancy & Finance is an exciting and developing profession!

As a consultant at Hays, you get the chance to make valuable contacts, test and get gain knowledge from different industries and above all, the chance to try out new tasks within Accountancy & Finance.

Our assignments vary as our customers operate in several industries, locally as well as globally.

As a consultant at Hays, you have a continuous dialogue with your Consultant Manager and meet regularly for follow-up and activities to give you support during the assignment and your continued career. We value a close partnership with our consultants to ensure that you enjoy and feel good in the role of consultant with us.

About Hays

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.

At Hays we invest in lifelong partnerships that empower people and businesses to succeed.

With over 50 years' success under our belts and a workforce of 10,000+ people across 33 countries, we've evolved to put our customers at the heart of everything we do.

So much more than a specialist staffing and recruitment business, what really sets us apart is our knowledge through scale, deep understanding and our ability to meaningfully innovate for our customers and candidates.

By providing advice, insights and expertise on issues you face today in the fast-paced world of work, we help you make the right decisions to achieve your goals. You can rely on us to deliver today and help you plan for tomorrow. Visa mindre

VGR/ Halland region.

Hays Life Sciences is now looking to recruit a Key Account Manager to join the Primary Care team within the AstraZeneca Nordic Marketing Company for an initial 6-month contract assignment from 2023-01-02 - 2023-06-30 with a view to a permanent position. This position will be to work within the VGR/ Halland region.

As part of AstraZeneca, the Nordic Marketing Company (Nordic) employs around 400 people across 5 countries and has offices located in Södertälje, Copenhagen, Helsinki and Oslo. By 2025 AstraZeneca Nordic aims to become a recognized leader in its core therapy areas and improve the lives of millions of people. This will be achieved by driving innovative science, preparing launches, building close collaboration and partnerships with key partners in health care systems, and developing high-performing teams.

We are looking for a Key Account Manager to join our Primary Care team to work with our exiting diabetes/cardio/renal and portfolio towards GP´s. Knowledge and experience within pharma industry sales is an success factor in this role but we also encourage applications from individuals with bio/medical experience outside pharma industry.

We offer you your next career move into a stimulating and growing company that keeps patients in focus. Let us know why you are the perfect match for us.

The roles is field based and located in VGR/Halland with responsibility for driving the performance of products in the working area. Your focus will be customers in primary care

As Key Account Manager, you will join AstraZeneca's strong CV-R-M franchise one of our key growth platforms. You will drive commercial interactions towards various partners. You will be accountable for your regional accounts securing sales and driving business in collaboration with both local and national cross-functional teams.

Accountabilities:

* Pro-actively identifying business opportunities, communicating value propositions aligned to stakeholder needs and objectives and recommending solutions to drive and develop business
* Develop robust understanding of needs and perceptions of prescribers and other key partners
* Drive cross-functional and cross-regional collaboration to leverage AZ's account management capabilities
* Secure account and market access by driving activities with the right customers within the right accounts
* Build, develop and lead long-term external relationships
* Drive and implement our digital and omnichannel approach towards our customers.

Essential requirements:

* We need you to hold an academic degree or equivalent with healthcare or commercial background. You have validated and relevant sales experience in pharma industry or other strong bio-medical background, preferentially but not required, within one or more of the disease areas; renal/diabetes/cardiovascular.
* Commercial innovation - ability of developing, shaping and implementing impactful, customer focused activities to achieve long-term business goals
* Leadership - ability to coordinate, align and engage in cross-functional teams to drive activities and address needs of individual accounts
* Ability and readiness to travel within region and according to role needs
* Driver´s license required and own car to use during work travels

At AstraZeneca, we embrace partnership, both internally and externally. You will fit well if you are a person that creates trust and possesses credibility.

Your proven ability to understand, assimilate, and communicate scientific information will be as important for the role as will your excellent communication skills, fluent in both written and spoken English and Swedish. You are patient focused, able to see issues through the lens of a patient as well as the patient journey and relevant treatment options.

Why AstraZeneca
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. Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be.

Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have seats available, and we hope it´s yours. Visa mindre

Associate Director, Diagnostic Project Management to AstraZeneca Gothenburg for a 1-year contract assignment.

he Diagnostic Project Management group within Precision Medicine, Project, Portfolio & Operations is accountable for providing project and portfolio management to the AZ Precision Medicine portfolio to ensure successful delivery of diagnostic projects from initiation of development to regulatory approval, across all therapy areas, and to further optimise the delivery of precision medicines by defining and championing best practices. Furthermore, this group is responsible for driving continuous improvement processes, for providing accurate Precision Medicine portfolio information for decision making and business reporting, and for capacity and resource management.
The Associate Director, Diagnostic Project Management will work across several cross-functional diagnostic project/ programme teams to provide hands on project management expertise to deliver projects within agreed time, budget and quality. The role depends on close collaboration with members of the Diagnostic Project Management Office, diagnostic project teams and external partners to ensure strategic alignment, and with Diagnostic Information Managers, who are responsible for inputting project information into AZ's enterprise planning tool (PLANIT).

Accountabilities/Responsibilities:


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

Minimum Requirements -Education and Experience
Education

* BA/BSc in relevant subject (or equivalent experience)

Minimum Experience Required

* Significant experience within a scientific project management environment
* Expert understanding of Project Management techniques, tools and principles
* Strong organisation and forward-planning skills, with attention to detail
* Experience of global team-working and effectively communicating with key stakeholders
* A professional, enthusiastic and proactive approach, with the ability to independently manage a diverse and demanding workload
* Experience of using Microsoft Office/ Outlook, project planning tools and web-based programmes
* Prior experience in managing and reporting of project information

Preferred Experience

* Professional project management qualification (e.g. PMP)
* High-level understanding and interest in Precision Medicine
* Experience of using PLANIT to accurately forecast resource and maintain milestones

Internal and External Contacts/Customers:
Internal

* Diagnostic Project Team (Precision Medicine Lead, Project Manager, Technical (Lab) Expert, Alliance Manager etc)
* Project, Portfolio & Operations team
* Diagnostic Project/ Portfolio Management Team
* Alliance Management team
* Precision Medicine teams
* R&D project teams (Oncology & BioPharmaceutical)
* Finance

External

* Diagnostic Partners
* Reporting Relationship:
* Reports to Head Diagnostic Project Management
* No direct reports

Budget responsibility

* Indirect responsibility for project budget

Measure of Success


* Diagnostic projects are delivered to cost, time and quality objectives
* Utilisation of best practice tools and processes by Diagnostic Project Teams
* Successful collaboration and close working relationships with Diagnostic Project Teams, Diagnostic Project Managers and Diagnostic Information Managers
* Accurate precision medicine, cost and resource information within enterprise planning tool (PLANIT)
* Successful running of Diagnostic Project team meetings leading to key decisions and effective action management to progress projects


Apply now for this opportunity or contact med for more info. Visa mindre

We are now looking for a Diagnostic Project Manager to AstraZeneca Gothenburg for 1-year contract assignment.

The Diagnostic Project Management group within Precision Medicine, Project, Portfolio & Operations is accountable for providing project and portfolio management to the AZ Precision Medicine portfolio to ensure successful delivery of diagnostic projects from initiation of development to regulatory approval, across all therapy areas, and to further optimize the delivery of precision medicines by defining and championing best practices. Furthermore, this group is responsible for driving continuous improvement processes, for providing accurate Precision Medicine portfolio information for decision making and business reporting, and for capacity and resource management. The Diagnostic Project Manager will work alongside the Assoc Director/ Director of Project Management r/ Associate Project Manager delivering technical expertise across several cross-functional diagnostic project and programme teams.

Accountabilities/Responsibilities:


* With direction: Manages projects within a franchise to deliver to time, cost and quality
* Creates and manages project plans to track and drive delivery of major milestones
* Manages project costs and resources (people)
* Creates and manages project risk logs, and drives mitigating actions where appropriate
* Creates progress reports to track delivery to time, cost and quality
* Works with, Diagnostic Information Managers to ensure efficient and effective management of project, programme and portfolio information
* Champions process simplification and standardization across Precision Medicine
* Meeting planning and facilitation
* Plan and facilitate Diagnostic Project Team meetings ensuring accurate actions are captured, circulated and followed up on.

Minimum Requirements -Education and Experience
Education

* BA/BSc in relevant subject (or equivalent experience)

Minimum Experience Required

* Understanding of Project Management techniques, tools and principles
* Strong organization and forward-planning skills, with attention to detail
* Experience of global team-working and communicating with key stakeholders
* A professional, enthusiastic and proactive approach, with the ability to independently manage a diverse and demanding workload
* Experience of using Microsoft Office/ Outlook and web-based programmes
* Prior experience in managing and provision of project information

Preferred Experience

* Professional project management qualification
* High-level understanding and interest in Precision Medicine
* Basic understanding or experience of using PLANIT

Internal and External Contacts/Customers:
Internal

* Diagnostic Project Team (Precision Medicine Lead, Technical (Lab) Expert, Alliance Manager etc)
* Project, Portfolio & Operations team
* Diagnostic Project Managers
* Diagnostic Information Managers
* Diagnostic Alliance Manager
* Portfolio Manager
* Portfolio Analyst
* Precision Medicine teams
* R&D project teams (Oncology & BioPharmaceutical)

External

* Diagnostic Partners

Reporting Relationship:


* Reports to Assoc Director, Diagnostic Project Management
* No direct reports

Budget responsibility

* Indirect responsibility for project budget

Measure of Success

* Diagnostic projects are delivered to cost, time and quality objectives
* Utilization of best practice tools and processes by Diagnostic Project Teams
* Successful collaboration and close working relationships with Diagnostic Project Teams, Project Managers and Information Managers
* Accurate data within PLANIT
* Successful running of Diagnostic Project team meetings leading to key decisions and effective action management to progress projects

Apply now for this opportunity or contact me for more info about the role. Visa mindre

KAM to AstraZeneca

Hays Life Science is now recruiting a KAM for a consulting assignment to AstraZeneca. The two positions are for the working areas "Sydöst" and "Väst". Send your application no later than August 18th.

We need you to hold an academic degree or equivalent with healthcare or commercial background. You have validated and relevant sales experience in pharma industry or other strong bio-medical background, preferentially but not required, within disease areas; heart failure/diabetes/cardiovascular and respiratory.

* Commercial innovation - ability of developing, shaping and implementing impactful, customer focused activities to achieve long-term business goals
* Leadership - ability to coordinate, align and engage cross-functional team to drive activities and address needs of individual accounts
* Ability and readiness to travel within region and according to role needs
* Driver´s license required and own car to use during work travels

Your proven ability to understand, assimilate, and communicate scientific information will be as important for the role as will your excellent communication skills, fluent in both written and spoken English and Swedish. You are patient focused, able to see issues through the lens of a patient as well as the patient journey and relevant treatment options.

You will fit well if you are a person that creates trust and possesses credibility. Visa mindre

Hays is looking for an Analytical Scientist for a 12-month contract assignment at AstraZeneca in Gothenburg.

Do you have an interest in analytical chemist? Would you like to work in a cross-functional environment using state of the art technology? Then you might be our next member in the Separation Science Laboratory team!

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

Main Duties and Responsibilities
You will join a highly competent team and collaboratively drive the delivery of pure compounds to our early portfolio. We use modern chromatographic instrumentation including LC and SFC in both analytical and preparative scale and a high degree of automation.To be successful in this role you will need a problem-solving attitude and strong delivery focus. It is essential with good communication skills and ability to engage and collaborate across boundaries.

You are expected to:
* Be laboratory based and work collaboratively with colleagues
* Run chromatographic equipment as well as liquid handling robotics
* Effectively operate with scientists from other functions in a highly cross-disciplinary environment

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

About Hays
At Hays we invest in lifelong partnerships that empower people and businesses to succeed. With over 50 years' success under our belts and a workforce of 10,000+ people across 32 countries, we've evolved to put our customers at the heart of everything we do.

So much more than a specialist staffing and recruitment business, what really sets us apart is our knowledge through scale, deep understanding and our ability to meaningfully innovate for our customers and candidates.
By providing advice, insights and expertise on issues you face today in the fast-paced world of work, we help you make the right decisions to achieve your goals.

You can rely on us to deliver today and help you plan for tomorrow. Visa mindre

Research Scientist - Mouse embryo manipulation

Hays Life Science is now recruiting a research scientist for a 9-month consulting contract at AstraZeneca in Gothenburg. Preferred starting date is September 1st. Send your application by August 12th at latest.

The Transgenics In Vivo model generation team has an immediate opening, to secure our business needs, for a skilled mouse embryologist. We provide mouse model generation services to all Therapy Areas within AstraZeneca. The main focus is on mouse model generation using Pro-nuclear injection, blastocyst injection, In Vitro Fertilization, IVF, and embryo transfer for rederivation of lines. The position is a contractor position lasting till end of May 2023.

Key responsibilities:
* Preparing pseudo pregnant females for surgery, performing Embryo Transfer surgeries, providing post-operative care to embryo recipients, and washing embryos by mouth pipette.
* Micro manipulation of mouse Zygotes by Pro -nuclear injection.
* Blastocysts injection of mouse embryonic stem cells
* Implantation surgery of embryos and blastocysts
* Perform In vitro fertilization
* Mouse embryonic stem cell transfection and clone picking
* Associated support duties including labelling and preparing culture dishes, managing lab supplies, maintaining lab equipment, and routine cleaning.
* Adheres to SOP, policies and procedures. Maintains work environment by cleaning, organizing and supplying their work space and areas within the department.
* Operates and monitors equipment in the assigned area. This may include microscopes, incubators, liquid nitrogen handling vessels, etc.
* Communicate with others in a proactive, professional, positive and supportive manner.

Requirements:
* Extensive experience in micro manipulation techniques, such as pro-nuclear injection, Blastocyst injection as well as implantation surgery in mice.
* Strong written and oral communication skills sufficient to permit clear and effective exchange of information with people representing a wide diversity of disciplines.
* Demonstrated computer software and database skills in Work, Excel, outlook , electronic lab book etc.
* You need to be a team player, flexible and able to adapt to changing business needs. Visa mindre