Remote Quality Manager (GCP/GVP) – Biotech

Cpl Life Sciences; High Wycombe; Hybrid; GBP 70,000 - 85,000; Part time

Benefits offered by this job

Fully remote

Global exposure

Biotech environment

Job summary

CPL Life Sciences is seeking a Temporary Quality Manager (GCP/GVP) to support global development quality in a biotech environment. This contract role requires expertise in GCP/GVP, quality system governance, and CAPA management.

You will partner with Global Development teams to drive regulatory compliance, oversee quality events, and lead investigations and data analysis across regions, while ensuring audit readiness and a strong quality culture.

Qualifications

• Bachelor's degree in a pharmaceutical, biotech, or healthcare field.
• Minimum of 6 years' experience in pharmaceutical/biotech or healthcare settings.
• Strong knowledge of GCP and/or GVP regulations and compliance.
• Experience managing QMS, quality events, governance processes, and continuous improvement.
• Experience conducting investigations and CAPA management.
• Experience as SME or process owner within quality functions; regulatory inspections support.

Responsibilities

• Partner with Global Development to drive process improvements and regulatory compliance.
• Manage quality metrics and trend reporting for continuous improvement.
• Oversee Quality Event portfolio and provide SME support to teams.
• Lead quality data analysis, root cause investigations, and CAPA implementation.
• Manage Quality System Metrics, reporting, thresholds, actions and effectiveness.
• Facilitate governance meetings and present QMS performance data.
• Coordinate procedural document reviews and impact assessments.
• Promote a strong quality culture across the organisation.
• Collaborate with cross-functional teams to strengthen QMS effectiveness.

Skills

Regulatory compliance

Communication

Project management

Stakeholder management

Education

Bachelor's degree

Job description

CPL Life Sciences is seeking a Temporary Quality Manager (GCP/GVP) to support global development quality in a biotech environment. This contract role requires expertise in GCP/GVP, quality system governance, and CAPA management.

You will partner with Global Development teams to drive regulatory compliance, oversee quality events, and lead investigations and data analysis across regions, while ensuring audit readiness and a strong quality culture.