The design, maintenance and effectiveness of the Stockton Quality Control Laboratorys pharmaceutical quality management system (QMS), in compliance with UK & EU Good Manufacturing Practice Developing and monitoring quality performance indicators (KPIs) and prepare regular reports for senior management. Designing and implementing an appropriate internal audit programme and coordinate external audits to assess QMS effectiveness Leading on specific research and development activities of the laboratory as directed by the lead pharmacist for Quality. The design, maintenance and effectiveness of the Validation Master Plan in accordance with GMP and other regulatory requirements. Coordinating, reviewing and approving validation activities related to facility, equipment and processes with EU GMP, MHRA, and other applicable regulatory standards.
Leading, mentoring, and developing a team of quality assurance and validation professionals. Participating in cross-functional meetings to integrate quality strategies with business objectives

Please refer the Job description for details