Clinical Quality Excellence Specialist — GCP/GVP & Inspections

VRS-UK; Slough; On-site; GBP 50,000 - 70,000; Full time

Job summary

A global biopharmaceutical organization in Slough is seeking an experienced Quality professional to join their Process Quality Excellence team. You will support the development of quality systems and ensure compliance with GCP and GLP standards. The ideal candidate has over 8 years of experience in the pharmaceutical sector and a proactive approach to quality assurance. The role is offered on an initial 12-month contract and includes responsibilities for audit coordination and maintaining inspection readiness.

Qualifications

• Minimum 8 years’ experience in the pharmaceutical sector.
• Strong knowledge of GCP and GVP.
• At least 2 years of experience writing SOPs.

Responsibilities

• Support the Head of Process Quality Excellence in quality frameworks.
• Create and revise quality policies and SOPs.
• Lead inspection readiness across clinical operations.

Skills

Quality assurance

Good Clinical Practice (GCP)

Regulatory Intelligence

Audit coordination

Job description

A global biopharmaceutical organization in Slough is seeking an experienced Quality professional to join their Process Quality Excellence team. You will support the development of quality systems and ensure compliance with GCP and GLP standards. The ideal candidate has over 8 years of experience in the pharmaceutical sector and a proactive approach to quality assurance. The role is offered on an initial 12-month contract and includes responsibilities for audit coordination and maintaining inspection readiness.