Remote Quality Manager (GCP/GVP) – Temporary (Biotech)

Cpl Life Sciences; Wakefield; Hybrid; GBP 70,000 - 85,000; Part time

Benefits offered by this job

Fully remote working arrangement

Global exposure

Job summary

Cpl Life Sciences is seeking an experienced Temporary Quality Manager (GCP/GVP) to support a global development quality function within a biotech environment. The role focuses on quality system governance, event oversight, and continuous improvement across a global organisation.

Key responsibilities include leading CAPA, data analysis, governance meetings, and collaboration with cross-functional teams to strengthen QMS effectiveness.

Qualifications

• Bachelor's degree and 6+ years in pharma/biotech/healthcare.
• Strong knowledge of GCP and/or GVP.
• Experience with QMS, quality events, governance, and continuous improvement.
• Experience conducting investigations and root cause analyses.
• Experience supporting regulatory inspections and audits.

Responsibilities

• Drive process improvements, standardisation, and regulatory compliance with Global Development stakeholders.
• Manage quality metrics and trend reporting for CI.
• Oversee the Quality Event portfolio and provide SME support to teams.
• Lead quality data analysis, CAPA development and implementation.
• Manage Quality System Metrics, reporting and effectiveness measures.
• Coordinate document reviews and impact assessments.
• Promote a strong quality culture across the organisation.
• Collaborate across functions to strengthen QMS effectiveness.

Skills

Quality Management

QMS

CAPA management

Regulatory inspections

Investigations

Stakeholder management

Education

Bachelor's degree

Job description

Cpl Life Sciences is seeking an experienced Temporary Quality Manager (GCP/GVP) to support a global development quality function within a biotech environment. The role focuses on quality system governance, event oversight, and continuous improvement across a global organisation.

Key responsibilities include leading CAPA, data analysis, governance meetings, and collaboration with cross-functional teams to strengthen QMS effectiveness.