Remote Quality Manager – GCP/GVP, Biotech (Temp)

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

Benefits offered by this job

Fully remote

Job summary

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

The ideal candidate has a Bachelor's degree and 6+ years in pharma/biotech, strong GCP/GVP knowledge, experience with QMS and CAPA, plus excellent communication and stakeholder management.

Qualifications

• Bachelor's degree with 6+ years in pharmaceutical/biotech
• Strong knowledge of GCP and/or GVP regulations
• Experience with Quality Management Systems (QMS) and CAPA
• Experience supporting regulatory inspections and audits
• Excellent communication and stakeholder management skills

Responsibilities

• Drive governance, regulatory compliance, and continuous improvement across a global development quality function
• Manage quality metrics and trend reporting to support CI activities
• Oversee Quality Event portfolio and provide SME guidance to teams
• Lead root cause investigations and CAPA development/implementation
• Manage Quality System Metrics, reporting, thresholds, actions, and effectiveness
• Coordinate procedural document 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

CAPA management

Regulatory compliance

Stakeholder management

Education

Bachelor's degree

Job description

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

The ideal candidate has a Bachelor's degree and 6+ years in pharma/biotech, strong GCP/GVP knowledge, experience with QMS and CAPA, plus excellent communication and stakeholder management.