Remote Quality Manager (GCP/GVP) - Temporary

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

Benefits offered by this job

Fully remote work option

Innovative biotech environment

Global exposure

Job summary

Cpl Life Sciences is recruiting a Temporary Quality Manager (GCP/GVP) to support a global development quality function within a biotechnology environment. Based in the UK, this hybrid/remote role is ideal for a quality professional with GCP/GVP experience to drive governance, compliance and continuous improvement.

You will partner with Global Development teams, manage quality events, CAPA, QMS metrics, and support regulatory inspections while mentoring colleagues and promoting a strong quality

Qualifications

• Bachelor's degree and minimum of 6 years' experience in pharma/biotech/healthcare.
• Experience in Quality Management, Quality Assurance, or Clinical Development environments.
• Strong knowledge of GCP and/or GVP regulations and compliance requirements.
• Experience with Quality Management Systems (QMS), quality events, governance processes, and continuous improvement.
• Experience conducting investigations, root cause analyses, and CAPA management.
• Experience acting as SME, Process Owner, or Business Process Owner in a quality function.
• Experience supporting regulatory inspections and audit readiness activities.
• Training/mentoring or supervising colleagues; strong communication and project management skills.

Responsibilities

• Partner with Global Development stakeholders to drive process improvements, standardisation and compliance.
• Manage quality metrics and trend reporting to support continuous improvement.
• Oversee the Quality Event portfolio and provide SME input to functional teams.
• Lead quality data analysis, root cause investigations and CAPA development/implementation.
• Manage Quality System Metrics, 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 QMS effectiveness and compliance.

Skills

Quality governance

Regulatory compliance

Stakeholder management

Project management

Data analysis

Education

Bachelor's degree

Tools

QMS

Job description

Cpl Life Sciences is recruiting a Temporary Quality Manager (GCP/GVP) to support a global development quality function within a biotechnology environment. Based in the UK, this hybrid/remote role is ideal for a quality professional with GCP/GVP experience to drive governance, compliance and continuous improvement.

You will partner with Global Development teams, manage quality events, CAPA, QMS metrics, and support regulatory inspections while mentoring colleagues and promoting a strong quality