Remote Quality Manager (GCP/GVP) – Biotech

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

Benefits offered by this job

Fully remote work

Global exposure

Job summary

Cpl Life Sciences seeks an experienced Temporary Quality Manager (GCP/GVP) to support a global development quality function in a biotechnology environment. This UK-based role offers hybrid/remote working as you drive governance, quality metrics, and CAPA across global teams.

You will bring 6+ years in pharma/biotech, strong GCP/GVP knowledge, and proven experience with QMS, investigations, CAPA, and regulatory readiness.

Qualifications

• Bachelor's degree and 6+ years in pharma/biotech.
• Experience with GCP/GVP regulations and compliance.
• Experience with QMS, governance, quality events and CAPA.
• Experience leading investigations and root cause analyses.
• Experience supporting regulatory inspections and audits.

Responsibilities

• Drive process improvements, standardisation, and regulatory compliance.
• Manage quality metrics and trend reporting for continuous improvement.
• Oversee Quality Event portfolio and provide SME support to teams.
• Lead quality data analysis, CAPA development and implementation.
• Manage Quality System Metrics, reporting and governance.
• Coordinate document reviews and impact assessments.

Skills

GCP/GVP knowledge

QMS management

CAPA management

Root cause analysis

Investigations

Stakeholder management

Project management

Education

Bachelor's degree in Pharmaceutical/Biotech

Tools

QMS software

Job description

Cpl Life Sciences seeks an experienced Temporary Quality Manager (GCP/GVP) to support a global development quality function in a biotechnology environment. This UK-based role offers hybrid/remote working as you drive governance, quality metrics, and CAPA across global teams.

You will bring 6+ years in pharma/biotech, strong GCP/GVP knowledge, and proven experience with QMS, investigations, CAPA, and regulatory readiness.