Temporary Quality Manager, GCP/GVP - Remote UK

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

Benefits offered by this job

Hybrid/Remote work

Global development exposure

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. Based in the UK with hybrid/remote flexibility, you will collaborate with Global Development to ensure regulatory compliance and quality oversight across the program.

You will lead CAPA, investigations, and governance activities, manage QMS metrics, and drive continuous improvement while developing strong stakeholder relationships.

Qualifications

• Bachelor's degree and a minimum of 6 years' experience in 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

Quality Assurance

Clinical Development

Regulatory inspections

CAPA management

QMS

Root cause analysis

Project management

Stakeholder management

Communication skills

Mentoring/training

Attention to detail

Prioritisation

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. Based in the UK with hybrid/remote flexibility, you will collaborate with Global Development to ensure regulatory compliance and quality oversight across the program.

You will lead CAPA, investigations, and governance activities, manage QMS metrics, and drive continuous improvement while developing strong stakeholder relationships.