Remote Quality Manager (GCP/GVP) - Contract

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

Job summary

Cpl Life Sciences seeks an experienced Temporary Quality Manager (GCP/GVP) to support a global development quality function within a biotechnology environment in the UK. Hybrid/Remote working and a temporary contract are on offer.

The role focuses on quality system governance, quality event oversight, CAPA management, and continuous improvement across a global organisation, requiring strong knowledge of GCP and/or GVP and QA experience in pharma/biotech.

Qualifications

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

Responsibilities

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

Skills

Quality management

GCP/GVP knowledge

Investigation & CAPA

Quality Event governance

Stakeholder management

Regulatory inspections readiness

Project management

Education

Bachelor's degree

Tools

Quality Management Systems (QMS)

Job description

Cpl Life Sciences seeks an experienced Temporary Quality Manager (GCP/GVP) to support a global development quality function within a biotechnology environment in the UK. Hybrid/Remote working and a temporary contract are on offer.

The role focuses on quality system governance, quality event oversight, CAPA management, and continuous improvement across a global organisation, requiring strong knowledge of GCP and/or GVP and QA experience in pharma/biotech.