GxP Third-Party Compliance Lead

WEP Clinical Inc.; United Kingdom; Remote; GBP 45,000 - 70,000; Full time

Benefits offered by this job

Group Private Medical Insurance

Group General Life Assurance

Group Critical Illness and Group In- s

Group Income Protection

Salary sacrifice pension scheme

Enhanced maternity & paternity pay

Paid volunteering day

Job summary

WEP Clinical is seeking a Third-Party Specialist to coordinate and monitor external partners supporting GxP activities. You will ensure documentation, qualification, and ongoing oversight of suppliers and contractors, enabling compliant, safe delivery of clinical services across trials and related operations.

The ideal candidate will have a relevant degree, 2–5 years in a regulated quality role, and strong collaboration skills to work with Quality, Regulatory, Clinical, and Operations teams.

Qualifications

• Bachelor’s degree in pharmaceutical/life sciences or engineering.
• 2–5 years’ experience in a Quality role within a regulated (GxP) environment.
• Hands-on experience in vendor/supplier management.
• Strong knowledge of GMP, GDP and relevant national regulations.

Responsibilities

• Manage qualification and requalification of suppliers and vendors with documentation.
• Maintain and update Approved Supplier and Vendor Lists.
• Coordinate third-party risk assessments, questionnaires and due diligence.
• Monitor supplier performance via metrics and periodic reviews.
• Support CAPAs related to third-party findings.
• Plan and coordinate internal and external audits with vendors.
• Review audit records and follow up on findings.
• Contribute to inspection readiness and act as SME when required.
• Collaborate with Quality, Regulatory, Clinical, and Operations teams.
• Drive improvements in third-party management processes and metrics.

Skills

Proactive

Cross-functional collaborator

Adaptable

Critical thinker

Education

Bachelor’s degree in pharmaceutical sciences, life sciences, or engineering

Job description

WEP Clinical is seeking a Third-Party Specialist to coordinate and monitor external partners supporting GxP activities. You will ensure documentation, qualification, and ongoing oversight of suppliers and contractors, enabling compliant, safe delivery of clinical services across trials and related operations.

The ideal candidate will have a relevant degree, 2–5 years in a regulated quality role, and strong collaboration skills to work with Quality, Regulatory, Clinical, and Operations teams.