Scientist Dmpk
Poolia Väst AB / Kemistjobb / Mölndal
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Do you want to support team a number of iMed projects at AstraZeneca? Do you want to develop scientific understanding? Do you want to transform ideas into workable opportunities? Then, it is you AstraZeneca is looking for.
This temporary role as laboratory based in-vitro ADME scientist will be responsible for design and conduct of laboratory projects/experiments, generate, interpret and report scientific data to support decision making in projects.
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.
The consulting assignment will start 2017-10-02 and go to 2018-06-30.
Are you the one we are looking for? Apply now - The recruitment process is already ongoing!
Arbetsuppgifter
The Arena:
Drug Safety and Metabolism is a function within Innovative Medicines and Early Development (iMed), AstraZeneca's small molecule biotech unit which deliver candidate drugs into late-stage clinical development. The role of Drug Safety and Metabolism is to characterize the non-clinical toxicology, off-target pharmacology and ADME properties of compounds.
The ADME, SATS teams are represented at both the Gothenburg and Cambridge research sites. ADME stands for absorption, disposition, metabolism and elimination, and we are responsible for delivering in-vitro data to understand concentration-effect-relationships in the several organs and enable quantitative prediction to the patient situation. We work with a breadth of ADME models covering a range of organs, including GI Tract, liver, kidney where we work to describe drug disposition, both transport and metabolism.
We are looking for a 9 months contingency worker, with a possible further extension to support the team make significant contributions to the success of a number of iMed projects, to develop our scientific understanding and to transform ideas into workable opportunities.
Tasks and responsibilities:
This temporary role as laboratory based in-vitro ADME scientist will be responsible for design and conduct of laboratory projects/experiments, generate, interpret and report scientific data to support decision making in projects.
The suitable candidate has a good understanding of the range of procedures relating to ADME in vitro systems. The work spans both data delivery from established assays, involvement in method development and in bespoke experimental research to rapidly respond to ADME issues. In collaboration with project representatives and other ADME in-vitro scientists, the role has opportunity to guide decision making in projects through delivering right quality experimental design and method development where required. It includes participation in cross-functional scientific forums, and where appropriate presentation of data at lab, section or department meetings and contribution to publications.
Utbildning/erfarenhet
Minimum requirements and key factors:
• Minimum Master 's degree or equivalent qualification
• Background in Pharmacy, Biology, Biochemistry, Medical Biosciences or similar
• Versatile in in-vitro, cell culture (use of caco-2 and transfected cell systems) laboratory skills (enzyme and transporter kinetic studies), handling of human cells and tissues
• Experience in bioanalytical techniques, e.g. LC-MS
• Good communication skills in English, both verbal and in writing are required
• Demonstrated ability to work in team and independently
Preferred experience:
• Experience in the area of absorption, drug metabolism and transport and disposition
• Experience from industry environment a plus, but not mandatory.
Förmåner
We take good care of our consultants and we offer social activities, as well as help in planning your future career. Your consultant manager is well experienced from your field, and knows how to get the most out of your assignment.
As a Poolia employee, you are included in the requirements concerning agreements on terms of employment by Unionen. Moreover, you get a grant for working out at your choice of place. You are also covered by a health insurance.
Företagsbeskrivning
Poolia 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.
Vår kunds hemsida
https://www.astrazeneca.com/ Sluttext
Does the consulting assignment sound interesting for you? Please apply even if you do not meet all minimum requirements and key factor requirements. In this recruitment, we will prioritize your personal qualities: social, earthy, team player, and curious together with your true passion for AstraZeneca and their medical products.
Varaktighet, arbetstid
Heltid Visstid, mer än 6 månader
Publiceringsdatum2017-08-15ErsättningFast lön
Så ansöker duSista dag att ansöka är 2017-08-22
Ange följande referens när du ansöker: 47449
Klicka på denna länk för att göra din ansökanKontaktJenny Lundkvist
jenny.lundkvist@poolia.seFöretagPoolia Väst AB
AdressPoolia Väst AB
Kungsgatan 42
41115 Göteborg
KontorsadressKungsgatan 42
Jobbnummer 3644183
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