Remote Quality Manager, GCP/GVP – Biotech

Cpl Life Sciences

Hemel Hempstead

Hybrid

GBP 70,000 - 85,000

Part time

9 days ago
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Benefits offered by this job

Fully remote working arrangement

Job summary

Cpl Life Sciences is seeking an experienced Temporary Quality Manager (GCP/GVP) to support a global development quality function within a biotech environment.

This role focuses on governance, compliance, and continuous improvement, requiring strong GCP/GVP knowledge and QMS experience. You will work across global teams, drive quality events, CAPA and metrics, and support regulatory readiness while maintaining a proactive quality culture.

Qualifications

  • Bachelor's degree and a minimum of 6 years' experience in pharma/biotech or healthcare.
  • Strong knowledge of GCP and/or GVP regulations and compliance requirements.
  • Experience with QMS, quality events, governance and CAPA processes.

Responsibilities

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

Skills

GCP/GVP expertise
Quality management
Regulatory inspections readiness
Root cause analysis
CAPA management
Stakeholder management
Project management
Communication skills
Mentoring/training
Organisational skills

Education

Bachelor's degree in life sciences

Job description

Cpl Life Sciences is seeking an experienced Temporary Quality Manager (GCP/GVP) to support a global development quality function within a biotech environment.

This role focuses on governance, compliance, and continuous improvement, requiring strong GCP/GVP knowledge and QMS experience. You will work across global teams, drive quality events, CAPA and metrics, and support regulatory readiness while maintaining a proactive quality culture.

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