Remote Quality Manager, GCP/GVP (Contract)

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

Benefits offered by this job

Fully remote

Job summary

Cpl Life Sciences is partnering with a biotechnology organisation to appoint a Temporary Quality Manager (GCP/GVP) to support global development quality functions. Based in the UK with hybrid/remote working options, the role drives governance, compliance and continuous improvement across the global quality system.

You will lead quality data analysis, CAPA management, oversee quality events, and collaborate with cross-functional teams to strengthen GMP/GCP compliance and readiness for regulatory

Qualifications

• Bachelor's degree and 6+ years' experience in pharmaceutical/biotechnology/healthcare.
• 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 activities.
• Experience conducting investigations, root cause analyses, and CAPA management.
• Experience as SME/Process Owner in a quality-related function.
• Experience supporting regulatory inspections and audit readiness.
• Previous experience training, mentoring, or supervising colleagues.
• Strong project management, organisational, and prioritisation skills.
• Excellent communication and stakeholder management abilities.

Responsibilities

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

Skills

Quality management

GCP/GVP knowledge

QMS / CAPA

Investigation & RCA

Audit readiness

Stakeholder management

Project management

Training & mentoring

Communication & presentation

Governance

Education

Bachelor's degree

Tools

QMS software

Job description

Cpl Life Sciences is partnering with a biotechnology organisation to appoint a Temporary Quality Manager (GCP/GVP) to support global development quality functions. Based in the UK with hybrid/remote working options, the role drives governance, compliance and continuous improvement across the global quality system.

You will lead quality data analysis, CAPA management, oversee quality events, and collaborate with cross-functional teams to strengthen GMP/GCP compliance and readiness for regulatory