Description
A mid-sized contract manufacturing company urgently requires an interim Qualified Person (QP) to support their sterile production operations in France.Location: Normandy, France
Duration: 6 months
Role and Responsibilities:
• Preparing final batch records of sterile products for final QP release to the European market
• Resolving any critical deviations and implementing relevant CAPAs
• Supporting audits and inspections
• Ensure that the site's quality procedures and systems are compliant with EU standards
Requirements:
• Experience working on batch release of pharmaceutical products (preferably QP certified)
• Fluent in French language (spoken and written)
• Experience working with sterile products and production processes, preferably within a batch release function
This is a highly challenging, but exciting position, which will have a long term impact on the production site. Apply now for further details.