CPL Life Sciences is seeking an experienced Temporary Quality Manager (GCP/GVP) to support a global development quality function within a biotechnology environment in the UK. Hybrid/Remote setup and a temporary contract.
You will drive QMS governance, manage quality events, CAPA, metrics, and regulatory continuity across global development, collaborating with cross-functional teams. Requires 6+ years in pharma/biotech QA with GCP/GVP exposure and strong communication.
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Remote Quality Manager, GCP/GVP (Biotech) – 6+ yrs in Milton Keynes employer: Cpl Life Sciences
Cpl Life Sciences is an exceptional employer, offering a dynamic work environment that fosters innovation and collaboration in the biotechnology sector. With a strong focus on employee growth and development, team members benefit from hybrid working arrangements in West London, allowing for a balanced work-life integration while contributing to groundbreaking projects in regulatory affairs. The company values continuous improvement and provides opportunities for meaningful contributions to the advancement of healthcare solutions.
