Main duties: - Responsible for products in QC- Write and revise analytical methods - Write and revise analytical specifications - Write and revise procedures - Write protocol and reports for validation of analytical methods - Write protocol and reports for stability studies - Support to our regulatory department - Support to QC analysis group - Write and approve deviations and change requests - Continues improvements
You need to have: - Minimum 5 years’ experience within pharma industry - Minimum 3 years’ experience within a quality function - Excellent communications skills both in Swedish and English - Bachelor/master degree in Chemistry, or equal - Excellent computer skills
If you are ready for a new challenge and want to work in an environment where you get many colleagues with a lot of experience and competence this could be the right position for you. We offer an workplace where both business and co-workers can grow, so if you feel that you want join our team, we look forward to your application. For more information please contact Barbara Willkomm, HR. For union information contact the local union chairman for Akademikerföreningen or Unionen,please call040-36 62 00 for support.We offer a permanent position,start dateto be agreed. We willreview application ongoing soplease submit your application as soon as possible. Latest day to apply is the 16 August 2019.