Remote Quality Manager (GCP/GVP) – Biotech

Cpl Life Sciences

Warrington

Hybrid

GBP 70,000 - 85,000

Full time

9 days ago
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Benefits offered by this job

Fully remote
Innovative environment
Global exposure
Impact on medicines

Job summary

Cpl Life Sciences is seeking a Temporary Quality Manager (GCP/GVP) to support a global development quality function in a biotech environment. The role focuses on governance, quality events, and continuous improvement across a global organisation.

The candidate will have GCP/GVP expertise, lead CAPAs, coordinate QMS metrics, and drive regulatory compliance while mentoring teams and promoting a culture of quality. Location is hybrid/remote within the UK.

Qualifications

  • Bachelor's degree in a relevant field and at least 6 years in pharma/biotech/healthcare.
  • Experience with Quality Management, QA, or Clinical Development environments.
  • Strong knowledge of GCP and/or GVP regulations and compliance requirements.
  • Experience managing QMS, quality events, governance processes, and improvements.

Responsibilities

  • Partner with Global Development to drive process improvements and regulatory compliance.
  • Manage quality metrics and trend reporting for continuous improvement.
  • Oversee the 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 document reviews and impact assessments.
  • Support a strong quality culture across the organisation.
  • Collaborate with cross-functional teams to strengthen QMS effectiveness and compliance.

Skills

Project management
Organisational skills
Prioritisation
Communication
Stakeholder management
Presentation skills

Education

Bachelor's degree

Tools

QMS

Job description

Cpl Life Sciences is seeking a Temporary Quality Manager (GCP/GVP) to support a global development quality function in a biotech environment. The role focuses on governance, quality events, and continuous improvement across a global organisation.

The candidate will have GCP/GVP expertise, lead CAPAs, coordinate QMS metrics, and drive regulatory compliance while mentoring teams and promoting a culture of quality. Location is hybrid/remote within the UK.

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