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

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

Benefits offered by this job

Fully remote working arrangement

Job summary

Cpl Life Sciences is seeking a Temporary Quality Manager (GCP/GVP) to support global development quality in a biotech environment. Hybrid/Remote in the UK, with a focus on quality governance, events, CAPA, and continuous improvement.

The ideal candidate has a bachelor's degree and 6+ years in pharma/biotech, strong GCP/GVP knowledge, and experience leading QMS, audits, and regulatory readiness within cross-functional teams.

Qualifications

• Bachelor's degree and at least 6 years' experience in pharma/biotech/healthcare.
• Experience in Quality Management, QA, or Clinical Development environments.
• Strong knowledge of GCP and/or GVP regulations and compliance.

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 Quality Management System effectiveness and compliance.

Skills

GCP knowledge

GVP knowledge

Quality management

Regulatory compliance

Stakeholder management

Project management

Communication skills

Education

Bachelor's degree in life sciences

Tools

Quality Management System (QMS)

CAPA process

Root cause analysis

Job description

Cpl Life Sciences is seeking a Temporary Quality Manager (GCP/GVP) to support global development quality in a biotech environment. Hybrid/Remote in the UK, with a focus on quality governance, events, CAPA, and continuous improvement.

The ideal candidate has a bachelor's degree and 6+ years in pharma/biotech, strong GCP/GVP knowledge, and experience leading QMS, audits, and regulatory readiness within cross-functional teams.