Cpl Life Sciences seeks an experienced Temporary Quality Manager (GCP/GVP) to support a global development quality function in a biotechnology environment. This UK-based role offers hybrid/remote working as you drive governance, quality metrics, and CAPA across global teams.
You will bring 6+ years in pharma/biotech, strong GCP/GVP knowledge, and proven experience with QMS, investigations, CAPA, and regulatory readiness.
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Remote Quality Manager (GCP/GVP) – Biotech 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.
