Description
A global pharmaceutical organisation is looking for a QA Specialist to support one of its manufacturing sites in Switzerland.This is a long term opportunity to support the compliance of a critical portfolio of products.
Location: Basel area, Switzerland
Duration: 12-24 months
Role and Responsibilities:
• Provide QA support to the production of solid dose pharmaceutical products (tablets, capsules and inhalers)
• Write Product Quality Reviews (PQR) and Annual Quality Reports (AQR)
• Compile data from product specifications, production batch records, process validation reports and CAPA reports
• Identify any adverse trends in the products or production processes
Requirements:
• Degree educated in Pharmacy, Chemistry, Biology or similar
• Fluent in German and English
• Experience writing PQRs for pharmaceutical products
• Knowledge of GMP regulations