Scientist /Senior Scientist
AstraZeneca Göteborg / Apotekarjobb / Mölndal
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hela Sverige AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world?s most serious diseases. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.
The arena
Pharmaceutical Technology and Development is accountable for delivering the design, innovative, efficient and robust processes for the manufacture of drug substance and product, the supply chain of products for safety and clinical trials and the generation of information and knowledge to ensure regulatory approval of new products.
Drug Product Manufacture (DPM) in Gothenburg manufactures investigational products (oral solution/suspension, parenteral solutions, capsules, tablets and inhalers) to AZ clinical studies mainly in phase I/II around the globe and is a vital part of the Pharmaceutical Supply Chain organisation. At DPM in the GMP (Good Manufacturing Practice) arena you will make an important contribution in delivering clinical results and new medicines.
The role
This role significantly contributes to the manufacturing of drug product in development phase for clinical studies. All below activities will have a significant impact on the speed, quality and cost of the AZ development portfolio.
• Responsible for the timely and cost effective manufacture of drug product in line with the plans agreed within DPM, with focus on practical hands-on work in our pilot plant GMP facilities.
• Strong technical competence, credibility and ability to give assured technical direction.
• Set up Master Manufacturing Records and Batch Records and perform transactions in Warehouse Management System through the Supply Chain IT-systems.
• Assess record and report manufacturing and validation data accurately according to GMP.
• Ensure SHE (Safety Health and Environment) and GMP standards are upheld and ensure AZ Policies and Standards are understood and followed.
• Establish and recommend ways to improve flexibility and productivity, including new ways of working, resulting in shorter lead times.
• Monitor and track relevant Key Performance Indicators (KPIs).
Minimum experience/requirements
We are looking for a professional scientist with good team working skills and the ability to operate independently to drive delivery of projects.
Experienced in parenteral product manufacture, equipment and processes is highly valued. This includes process validation and knowledge of sterilisation processes to support validation activities.
BSc/MSc in pharmacy or engineering (specialising in Pharmaceuticals) and /or experience from pharmaceutical development or working in a manufacturing or supply chain organisation is required. You will have knowledge of GMP and SHE and excellent documentation skills, both in English and Swedish. You will also have good understanding and interest in manufacturing equipment.
More information
For more information about the position please contact:
Gunnar Haeffler or Bodil Egeland at +46 31 776 10 00.
Welcome with your application, via
www.astrazeneca.se no later than February 14th.
Varaktighet, arbetstid
Tillsvidare
Heltid
Publiceringsdatum2016-01-21ErsättningFast månads- vecko- eller timlön
Så ansöker duSista dag att ansöka är 2016-02-14
Ange följande referens när du ansöker: GOT0000002B
FöretagAstraZeneca Göteborg
AdressAstraZeneca Göteborg
43183 MÖLNDAL
KontorsadressPEPPAREDSLEDEN 1
MÖLNDAL
Övriga kontaktuppgifterTelefonnummer: 031-7761000
Jobbnummer 2628007
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