MSI Pharma are working with one of the top pharma companies in the world to hire a Quality Engineer for a 12 month contract in Switzerland.

Tasks & Responsibilities:

Supports the Product Release Monitoring and Strategic Collaborator Employee Certification Program.
Reviews and approves key quality records as they related to MD products in accordance to the Quality Agreement, such as:
o Nonconformance records (incl. CAPAs and Product Dispositions),
o Site Validation Master Plan and Validation protocols,
o Inspection plans and associated sampling strategies,
o Where necessary, collaborate in failure investigation and corrective action planning involving MD products.
Coordinates MD review of nonconformance disposition in collaboration with other required MD functions ( Supports Strategic Collaborators Quality and Manufacturing Engineering on the resolution of quality issues impacting MD products and coordinates additional subject matter expert support needed from MD.
Initiates Stop Shipments and Product Issue Escalations for products out of MD control.
Supports improvement plans to address below-target metrics and negative trends.
Serves as the Source Quality Manager deputy.