Global GCP/GVP Quality Manager – Remote

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

Benefits offered by this job

Fully remote work arrangement

Job summary

Cpl Life Sciences is seeking a Temporary Quality Manager (GCP/GVP) to support global development quality within a biotech setting. You will governance, oversee quality events, and drive CAPA improvements across a global organisation.

The role requires strong GCP/GVP expertise, quality systems experience, and the ability to lead cross-functional collaboration. Based in the UK with a fully remote/hybrid arrangement, you will partner with Global Development teams to ensure regulatory compliance and

Qualifications

• Bachelor's degree and at least 6 years in the pharmaceutical, biotechnology, or healthcare industry.
• Experience in 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.

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

Regulatory inspections readiness

Stakeholder management

Education

Bachelor's degree

Job description

Cpl Life Sciences is seeking a Temporary Quality Manager (GCP/GVP) to support global development quality within a biotech setting. You will governance, oversee quality events, and drive CAPA improvements across a global organisation.

The role requires strong GCP/GVP expertise, quality systems experience, and the ability to lead cross-functional collaboration. Based in the UK with a fully remote/hybrid arrangement, you will partner with Global Development teams to ensure regulatory compliance and