Senior Analyst

Arbetsbeskrivning

Novozymes Biopharma Sweden AB is a subsidiary of Novozymes A/S and is a CMO (contract manufacture organization) of API (active pharmaceutical ingredient) towards the pharmaceutical and biotechnical industry.Furthermore, the company is engaged in developing manufacturing processes for our clients.The company is compliant with GMP since 1994.Currently our staff consists of 100 employees, whereof eight are working within the Quality Control department.Challenges You will under supervision from the QC Manager and the Project Manager independently work, drive and take responsible for activities within the production, development and analyses needed for cell bank manufacturing.This involves a close cooperation and communication with different departments and project teams.You will be involved in writing and reviewing SOP s and qualification/validation documents as well as practical laboratory work.All work is done according to GMP.Qualifications We believe that you have at least a Bachelor degree or equivalent education within the microbiological/biochemistry field.It is essential that you have experience and a keen interest in cell bank activities preferably from the biotech industry.Experience from GMP is a must.Since we operate in an international environment you must be able to document and communicate in both Swedish and English.Candidates should posses good social skills and be strong team players.It is also important to be well organized, driving, independent and accurate.The employment is a temporary position starting as soon as possible and ending in October 2010. Please apply online before July 13th.

Sammanfattning

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21 januari 2006

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