A Biopharmaceutical company specializing in the development and manufacturing of new vaccines, therapeutic proteins, and enzyme products are essentially looking for a QP on a permanent basis to join their dynamic QA team.

Roles and responsibilities include but are not limited to:

• Review batch manufacturing documentation to ensure compliance with EU GMP and the Product Specification File/marketing authorization
• Certify Medicinal products for use in the EU and outside the EU
• Undertake audits in EU and third countries
• Provide advice and guidance to staff and customers regarding pharma regulations.
• Provide technical and quality input to projects related to products, facilities, and equipment.
• To provide input and assistance with relevant elements of the Quality Management System (QMS) within the business.

Eligible candidates will possess the following:

• Steriles and/or biologics experience
• QP certification
• Minimum of 1 year in batch release