Temporary Global Quality Manager, GCP/GVP – Remote

Cpl Life Sciences; Bournemouth; Hybrid; GBP 70,000 - 85,000; Part time

Benefits offered by this job

Fully remote working arrangement

Job summary

CPL Life Sciences seeks a Temporary Quality Manager (GCP/GVP) in the UK to support a global development quality function within a biotech environment. You’ll drive governance, regulatory compliance, and continuous improvement across a global organisation.

With 6+ years in QA/quality management, you will lead CAPA activities, investigations, and QMS initiatives, collaborating with cross-functional teams and regulatory bodies. This is a hybrid/remote UK-based role.

Qualifications

• Bachelor's degree in the pharmaceutical/biotech/healthcare arena.
• 6+ years' experience in quality management, QA, or clinical development.
• Strong knowledge of GCP and/or GVP regulations and compliance.

Responsibilities

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

Skills

GCP

GVP

Quality Management

QMS

CAPA

Root Cause Analysis

Regulatory Inspections

Audit Readiness

Training & Mentoring

Project Management

Stakeholder Management

Communication

Education

Bachelor's degree in a relevant field

Tools

QMS

Job description

CPL Life Sciences seeks a Temporary Quality Manager (GCP/GVP) in the UK to support a global development quality function within a biotech environment. You’ll drive governance, regulatory compliance, and continuous improvement across a global organisation.

With 6+ years in QA/quality management, you will lead CAPA activities, investigations, and QMS initiatives, collaborating with cross-functional teams and regulatory bodies. This is a hybrid/remote UK-based role.