Remote Quality Leader – GCP/GVP (Biotech)

Cpl Life Sciences; Woking; Hybrid; GBP 70,000 - 85,000; Part 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 a global development quality function within a science-led biotechnology environment.

This role focuses on quality system governance, quality event oversight, compliance activities, and continuous improvement initiatives across a global organisation, leveraging strong knowledge of GCP and/or GVP regulations.

You must be based in the UK; the role offers hybrid/remote working options (Uxbridge/London area).

Qualifications

• Bachelor's degree and a minimum of 6 years' experience within the pharmaceutical, biotechnology, or healthcare industry.
• Experience within Quality Management, Quality Assurance, or Clinical Development environments.
• Strong working 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 activities.
• Experience conducting investigations, root cause analyses, and CAPA management.
• Experience acting as a Subject Matter Expert, Process Owner, or Business Process Owner within a quality-related function.
• Experience supporting regulatory inspections and audit readiness activities.
• Previous experience training, mentoring, or supervising colleagues.
• Strong project management, organisational, and prioritisation skills.
• Excellent communication, stakeholder management, and presentation abilities.
• A proactive approach with strong attention to detail and the ability to manage multiple priorities effectively.

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/GVP knowledge

Quality management

CAPA management

Root cause analysis

Regulatory compliance

Project management

Stakeholder management

Documentation governance

Education

Bachelor's degree

Job description

CPL Life Sciences is seeking a Temporary Quality Manager (GCP/GVP) to support a global development quality function within a science-led biotechnology environment.

This role focuses on quality system governance, quality event oversight, compliance activities, and continuous improvement initiatives across a global organisation, leveraging strong knowledge of GCP and/or GVP regulations.

You must be based in the UK; the role offers hybrid/remote working options (Uxbridge/London area).