Remote Quality Manager (GCP/GVP) – Biotech

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

Benefits offered by this job

Fully remote work

Global exposure

Biotech environment

Job summary

Cpl Life Sciences is seeking an experienced Temporary Quality Manager (GCP/GVP) to support a global development quality function in a biotechnology environment. The role is UK-based with hybrid/remote work.

You will oversee quality governance, event oversight, CAPA management, and continuous improvement initiatives across the global organisation, ensuring GCP/GVP compliance and effective Quality System performance with cross-functional teams.

Qualifications

• Bachelor's degree in a relevant field or equivalent experience.
• Minimum 6 years in pharmaceutical/biotech/healthcare quality roles.
• Strong knowledge of GCP and/or GVP regulations and compliance.
• Experience with QMS, quality events, governance, and CAPA processes.
• Experience in investigations and root-cause analyses with corrective actions.

Responsibilities

• Partner with Global Development stakeholders to drive process improvements and regulatory compliance.
• Manage quality metrics and trend reporting to support continuous improvement.
• Oversee the Quality Event portfolio and provide SME support to teams.
• Lead quality data analyses, root-cause investigations, and CAPA development.
• Manage Quality System Metrics, reporting, and effectiveness measures.
• Facilitate governance meetings and present MYS data to stakeholders.
• Coordinate procedural reviews and impact assessments.
• Support and promote a strong quality culture across the organisation.
• Collaborate to strengthen QMS effectiveness and compliance.

Skills

GCP/GVP knowledge

Quality management

Quality assurance

Investigations & CAPA

Project management

Stakeholder management

Communication

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 in a biotechnology environment. The role is UK-based with hybrid/remote work.

You will oversee quality governance, event oversight, CAPA management, and continuous improvement initiatives across the global organisation, ensuring GCP/GVP compliance and effective Quality System performance with cross-functional teams.