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WEP Clinical

Specialist services for early access medicines

Third Party Specialist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeNo salary listed

About the Job

Requirements

  • A bachelor's degree is required; a degree in pharmaceutical sciences, life sciences, or engineering is preferred.
  • Two to five years of experience in a Quality role within a regulated GxP environment.
  • Hands-on experience in vendor or supplier management.
  • Strong knowledge of Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and relevant national regulations.
  • Strong organisational skills and attention to detail.
  • Effective written and verbal communication skills.
  • Ability to manage multiple priorities and meet deadlines under pressure.
  • Strong critical-thinking skills and a proactive, solutions-driven mindset.
  • Strong interpersonal skills and ability to collaborate across teams.
  • High integrity and discretion when handling confidential information.

Responsibilities

  • 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.

About the Company

WEP Clinical

Specialist services for early access medicines

WEP Clinical provides access to unlicensed or scarce medicines through Expanded Access Programs (EAP) and Managed Access Programs (MAP) for healthcare providers in 60+ countries. It designs and runs these programs, coordinates with manufacturers and regulators, and sources medicines via a global network, with import authorizations and logistics handled by country managers and in-house pharmacists. Its approach combines global sourcing with local expertise and an end-to-end program model, differentiating it from others that rely on limited markets or suppliers. Its goal is to deliver needed treatments quickly when options are unavailable.

Company size
201-500
Company stage
Not listed
Total funding
Not listed
Headquarters
London, United Kingdom
Founded
2008

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