Quality Assurance Manager- Pharma-Zug-Contract

We are currently looking to get in touch with Quality Assurance Professionals with experience in GCP and GPvP to introduce to our client, a world leading pharmaceutical company in Switzerland that is going to add weight to your profile by adding to your skills and experience whilst learning from one of the industry's best , increasing your employability prospects.

Our client is looking for a Quality Assurance Development Manager that is going to be responsible for Good Clinical Practice (GCP) and Good Pharmacovigilance Practice (GPvP) oversight and for assuring quality and compliance of Development and Medical Affairs (MA) projects, products and programs (Phase I through Phase IV), as well as GxP activities related to Marketing. This first Introductory 9 months assignment would offer you the opportunity to add to your skills in quality assurance, pharmacovigilance and clinical development whilst learning from one of the industry's best during this long and stable assignment, which will give you time to forecast next career opportunities.

Your major accountabilities would be:

• Audit management
• Inspection management
• Deviations and Issues Management
• Management of vendors in the GCP / PV area as well as for Patient Oriented Programs (POPs)
• Release activities
• SOP Management

The Key successful requirements are:

• Degree in Life Sciences or related fields
• 3 years' experience in the pharmaceutical industry in a relevant field such as quality assurance, pharmacovigilance, clinical development or a directly related area.
• Strong project management skills, GCP and PV knowledge
• English fluent in speaking and writing, other languages are an asset

Send your profile across to Alex at a.arjocan@nonstopconsulting.com so he can give you more details about the role!

We have limited interview slots for the next days, so if this is of interest, apply today to give yourself the best chance.