Temporary QA Manager (GCP/GVP) – Remote UK

Cpl Life Sciences; Uxbridge; Hybrid; GBP 70,000 - 85,000; Full time

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, events oversight, and continuous improvement across a global organisation.

You will apply strong GCP/GVP knowledge to drive regulatory compliance, metrics, and CAPA initiatives within a global team.

Qualifications

• Bachelor’s degree and at least 6 years in pharma/biotech.
• Experience in Quality Management and QA or Clinical Development.
• Strong knowledge of GCP and/or GVP regulations.
• Experience leading QMS, governance, and CAPA activities.

Responsibilities

• Drive process improvements, standardisation, and regulatory compliance.
• Manage quality metrics and trend reporting.
• Oversee Quality Event portfolio and SME to teams.
• Lead CAPA development and implementation.
• Manage Quality System Metrics and governance reporting.
• Coordinate procedural reviews and impact assessments.
• Promote a strong quality culture and cross-functional collaboration.
• Collaborate to strengthen QMS effectiveness and compliance.

Skills

GCP/GVP expertise

Quality Management

CAPA management

Regulatory inspections

Stakeholder management

Education

Bachelor's degree

Tools

QMS

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, events oversight, and continuous improvement across a global organisation.

You will apply strong GCP/GVP knowledge to drive regulatory compliance, metrics, and CAPA initiatives within a global team.