As a Quality Specialist collaborator, you will be in charge of the tracking, reporting, monitoring and operational execution with internal and external partners. Your main tasks will be to:
Collect and prepare documentation for batchrelease
Publish documentation in databases
Review and approval of packaging component and the master packaging records
QA assessment of Product Returns
Assist Processing of Change Controls and deviations
Develop and maintain a dashboard for Global Commercial QA Operations standard
Support the revision of Quality and Technical Agreements with third party Contractors
Support the implementation and maintenance of product specifications
Support preparation of Annual Product Reviews
Follow-up of Audit CAPAs
Leading global biopharmaceutical company Quick onboarding - Possibility of internal growth
You have a Bachelor or a Master degree in Life Sciences, Medical Technologies or Engineering
You are immediately available and you have been working for at least the last 2 years in a QA department - background experience with Medical Device environment would be considered as well
You must be fluent in English. German and French is an asset
Our client is a leading global biopharmaceutical American company based in Vaud County in Switzerland. Our client recruits dynamic and innovative science-oriented people. Middle-sized company, as a Temp contractor you will have a strong impact on activities and colleagues relationship.
