We are currently searching for a QA Specialist - Project Manager for one of our clients, a global bio-pharmaceutical company located in Switzerland.
Responsibilities:
- As a member of the quality assurance team, you will be responsible to ensure production of API`s is in accordance with Good Manufacturing Practice
- Support the contract manufacturing and advise members of development, production and analytical departments on all aspects of GMP
- Responsible for checking manufacturing documentation for conformity, processing of change controls and reviewing and approving of deviations and OOS-results
- GMP audits support
Key requirements:
- A degree in Life Science (microbiology, biotechnology, chemistry)
- Relevant experience in the biopharmaceutical industry, ideally in GMP area
- Strong communication skills, experience in working with stakeholders from different departments
- Experience with TrackWise, SAP, LIMS and DMS is a plus
- English fluent, German fluen (Mandatory)
For further information about this position, please apply with your CV.
*Please note, only those with the right to work in Switzerland can apply!
