QA Senior Specialist

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 six are working within the Quality Assurance department.Challenges For the right candidate we offer a challenging position where you with reference to the QA manager work independently and are expected to drive and be responsible for compliance questions in the production, development and analyses.This involves a close cooperation and communication with different departments, project teams and customers.You will be involved in reviewing, approving SOP s and documents as well as being the QA representative in projects.All work is done according to GMP.Qualifications The successful candidate has a Master of Science degree in pharmacy, chemistry or equivalent education within the scientific/technical field.It is essential that you have experience and a keen interest in production including cell banks preferably from the pharmaceutical or biotech industry.The position might involve release of API, processing aids and cell banks and hence experience from release, clean room, cell banks will be a benefit.Experience from working in a GMP environment is a must.Since we operate in an international environment you must be able to document and communicate in both Swedish and English.Contact The applicant must have personal drive combined with a structured and accurate approach to as well as good communications and collaborations skills. The employment is a permanent position starting as soon as possible. Please apply online before 2009-08-17