QA Specialist

Novozymes Biopharma Sweden AB is a subsidiary of Novozymes A/S performing microbiologically based contract manufacturing of active pharmaceutical ingredients (APIs).Our main customers are industries within the pharmaceutical and biotech area.We are situated in Lund, Sweden, where we have modern laboratories and production facilities.The number of employees today is 92, whereof 7 are working in the Quality Assurance Department. Challenges You will under supervision from the QA Manager independently work, drive and be responsible for compliance questions in the production, development and for analyses.This involves a close cooperation and communication with different departments and project teams.You will be involved in reviewing, approving SOP s and documents as well as being the QA representative in different projects.You will also be responsible for one or several QA systems eg.deviation system, change control system.All work is done according to GMP.Qualifications We believe that you have 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 technique/production preferably from the pharmaceutical or 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 June 2010. Please apply online February 18th