Remote Contract Quality Manager - GCP/GVP (Biotech)

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

Benefits offered by this job

Fully remote working arrangement

Job summary

CPL Life Sciences seeks an experienced Temporary Quality Manager (GCP/GVP) to support a global development quality function in a biotech environment. The role focuses on governance, compliance, and continuous improvement across a global organisation.

Ideal candidates have 6+ years in pharma/biotech, strong GCP/GVP knowledge, and a proactive, detail-oriented approach. This is a hybrid/remote UK-based position offering a competitive salary and exposure to global quality functions.

Qualifications

• Bachelor's degree and a minimum of 6 years' experience in the pharmaceutical/biotech/healthcare sector.
• Experience in Quality Management, Quality Assurance, or Clinical Development environments.
• Strong knowledge of GCP and/or GVP regulations and compliance requirements.
• Experience managing or supporting Quality Management Systems (QMS), quality events, governance processes, and continuous improvement.

Responsibilities

• Drive process improvements, standardisation, and regulatory compliance with Global Development stakeholders.
• Manage quality metrics and trend reporting for continuous improvement.
• Oversee the Quality Event portfolio and provide SME input to cross-functional teams.
• Lead quality data analysis, root cause investigations, and CAPA development and implementation.
• Manage Quality System Metrics, including reporting, thresholds, actions, and effectiveness.
• Facilitate governance meetings and present Quality Management System performance data.

Skills

GCP knowledge

GVP knowledge

Project management

Stakeholder management

CAPA management

Root cause analysis

Education

Bachelor's degree

Job description

CPL Life Sciences seeks an experienced Temporary Quality Manager (GCP/GVP) to support a global development quality function in a biotech environment. The role focuses on governance, compliance, and continuous improvement across a global organisation.

Ideal candidates have 6+ years in pharma/biotech, strong GCP/GVP knowledge, and a proactive, detail-oriented approach. This is a hybrid/remote UK-based position offering a competitive salary and exposure to global quality functions.