Third Party Specialist

Are you looking for an exciting and fulfilling new position? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring ideas that make a real difference. Be part of a mission-driven organisation dedicated to advancing clinical research and transforming lives.

The Third-Party Specialist willbe responsible forthe day-to-day coordination, documentation, and monitoring ofthird parties (i.e. suppliers andthird-party contractors/vendors) supporting the company’sGxPactivities. This includes qualification, ongoing performance monitoring, and compliance oversightofthird parties involved in pharmaceutical manufacturing, distribution, clinical operations,nursing and related support services. The role ensures thatall third partiesoperatein accordance with applicable regulatory requirements and company standards, enabling the safe, effective, and compliant delivery ofWEP Clinical services(e.g.across Expanded Access Programs, Clinical Trial management and supply, and nursing operations).

• Proactive and solutions-driven
• Critical thinker
• Cross-functional collaborator
• Adaptable

• Manage the qualification and requalification of suppliers and vendors, ensuring all required documentation is in place.
• Maintain and update Approved Supplier and Vendor Lists in line with company procedures.
• Coordinate third-party risk assessments, questionnaires, and due diligence checks.
• Monitor supplier performance through metrics and periodic reviews, escalating issues when needed.
• Support and track corrective and preventive actions (CAPAs) related to third-party findings.
• Help plan and coordinate internal and external audits, including liaising with vendors and auditors.
• Review and maintain audit records, ensuring timely follow-up on findings.
• Contribute to inspection readiness activities and act as a Subject Matter Expert when required.
• Work closely with Quality, Regulatory, Clinical, and Operations teams to ensure third-party compliance supports business needs.
• Drive improvements in third-party management processes and provide quality metrics to support business decisions.

• Bachelor’s degree (preferably in pharmaceutical sciences, 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
• Excellent organisational skills and attention to detail
• Effective written and verbal communication skills
• Ability to manage multiple priorities and meet deadlines under pressure
• Proactive, solutions-driven mindset with strong critical thinking skills
• Strong interpersonal skills and the ability to collaborate across teams
• High level of integrity and discretion when handling confidential information

• Group Private Medical Insurance
• Group General Life Assurance
• Group Critical Illness and Group Income Protection
• Salary sacrifice pension scheme
• Enhanced maternity & paternity pay
• Paid volunteering day

WEP Clinical partners with biopharmaceutical Sponsors to help them bring treatments closer to the patients who need them most. Through end-to-end clinical trial delivery, home health services, expanded access programs, and market access consultancy, we provide flexible, fit-for-purpose solutions that support drug development, improve access, and help therapies reach the right patients at the right time. With more than 15 years of global experience, we have supported programs across 150+ countries, combining operational scale with the agility…