QC Materials Manager

About the role

The QC Manager will be managing a team of QC Analysts working with incoming materials and ensuring GMP compliant activities for the QC release of ATMP biotechnology products.

This role will be a key part of aiding the GMP facility in the production of gene therapy products for the ophthalmology, oncology, and neurology areas.

Responsibilities

• Provide line management to member(s) of the incoming material inspection department to contribute to the overall group objectives
• Overseeing the incoming material inspection department to support the seamless supply of materials for the manufacture of drug products
• Support the development and implementation of quality control documentation/continuous improvement programmes
• Contribute to the training and development of team members
• Support & participate in Safety assessments, job hazard assessments, and FMEAs relevant to warehouse operations and material movement
• Ensure all incoming material documentation meets GMP requirements

Requirements

• Supervisory and management experience of people and processes
• Minimum four years experience working in a GMP environment in a scientific discipline
• Experience in quality documentation (SOP, CAPA, deviation, batch records) and batch release
• Proficiency in Microsoft Office software, specifically Word, Excel and PowerPoint.
• Previous experience working in a fast-paced manufacturing environment
• Availability to work 5 days weekly on-site