Remote Quality Manager, GCP/GVP (Biotech) – 6+ yrs

Cpl Life Sciences; Milton Keynes; Hybrid; GBP 70,000 - 85,000; Part time

Benefits offered by this job

Fully remote

Job summary

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.

Qualifications

• Bachelor’s degree in pharmaceutical/biotech or related field.
• Minimum of 6 years’ experience in pharmaceutical, biotech, or healthcare QA.
• Strong knowledge of GCP and/or GVP regulations.
• Experience with Quality Management Systems (QMS) and CAPA management.
• Experience supporting regulatory inspections and audit readiness.

Responsibilities

• Partner with Global Development stakeholders to drive process improvements, standardisation, and regulatory compliance.
• Manage quality metrics and trend reporting to support continuous improvement activities.
• Oversee the Quality Event portfolio and provide subject matter expertise to functional teams.
• Lead quality data analysis, root cause investigations, and CAPA development and implementation.
• Manage Quality System Metrics, including reporting, thresholds, actions, and effectiveness measures.
• Facilitate governance meetings and present Quality Management System performance data to stakeholders.
• Coordinate procedural document reviews and impact assessments.
• Support and promote a strong quality culture across the organisation.
• Collaborate with cross-functional teams to strengthen Quality Management System effectiveness and compliance.

Skills

GCP/GVP knowledge

Quality management

Quality assurance

Project management

Communication

Education

Bachelor's degree

Tools

QMS software

Job description

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.