Skip to main content

Wepclinical

Third Party Specialist

London, England, United Kingdom +1

Location
Chiswick, United Kingdom · United Kingdom
Work
Hybrid
Employment
Full-time
Level
Not stated
Function
Other
Pay
Not stated
Posted
14 months ago

About the role

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.

Role Objectives

The Third-Party Specialist will be responsible for the day-to-day coordination, documentation, and monitoring of third parties (i.e. suppliers and third-party contractors/vendors) supporting the company’s GxP activities. This includes qualification, ongoing performance monitoring, and compliance oversight of third parties involved in pharmaceutical manufacturing, distribution, clinical operations, nursing and related support services. The role ensures that all third parties operate in accordance with applicable regulatory requirements and company standards, enabling the safe, effective, and compliant delivery of WEP Clinical services (e.g. across Expanded Access Programs, Clinical Trial management and supply, and nursing operations).

The Ideal Candidate

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

What You'll Do

  • 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.

What You'll Need

  • 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

What We Offer

Group Private Medical Insurance

Group General Life Assurance

Group Critical Illness and Group Income Protection

Salary sacrifice pension scheme

Enhanced maternity & paternity pay

Educational Assistance allowance

Paid volunteering day

What Sets Us Apart

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 and personalised service of a specialised provider. Our work helps bridge critical gaps in care, ensuring safe, ethical, and efficient access to promising new treatments.

We're Committed to Our Team

WEP has many initiatives to encourage wellness, growth, development, and team relationships. Check out our LinkedIn life page to learn more about our team events and all that we do to support our employees.

How We Work at WEP Clinical

At WEP Clinical, we look for individuals who are conscientious, exercise sound judgement, and engage with others thoughtfully and professionally. We believe excellence is achieved through integrity, accountability, and respect for diverse perspectives – and we are committed to helping our people grow and succeed in an inclusive, supportive environment.

Our Services Include

Access Programs

Clinical Trial Services

Patient Site Solutions

Clinical Trial Supply

Market Access and Commercialization

Data Privacy Notice

WEP Clinical is committed to protecting your personal information throughout the recruitment process. By applying, you acknowledge that your personal data will be processed in accordance with our Privacy Policy and Job Applicant Privacy Notice.

Privacy Policy: https://www.wepclinical.com/privacy-policy/

Job Applicant Privacy Notice: https://www.wepclinical.com/Job-Applicant-Privacy-Notice/

How to Apply

To be considered for this role, please submit your resume through the WEP Clinical Careers Portal or by using LinkedIn’s Easy Apply option. Please ensure your resume is in English.

Important Note

To streamline our hiring process, we use an Upwage AI screener. If you receive a link from Upwage, it is a legitimate part of our application process and helps ensure every candidate is reviewed consistently. If you are selected to move forward after the screener, a member of our team will contact you directly from an @wepclinical.com email address to guide you through the next steps of the interview process. Please ensure you apply only through our official careers page (https://www.wepclinical.com/careers/) or our verified LinkedIn page.

For Your Safety, Please Note

We will never communicate with you via Microsoft Teams or text message.

We will never ask for your bank account information at any stage of recruitment.

WEP Clinical is a smoke-free, drug-free, and alcohol-free work environment.

WEP Clinical is an equal-opportunity employer. WEP Clinical does not unlawfully discriminate against employees or applicants for employment based on an individual’s race, colour, religion, creed, sex, sexual orientation, gender identity or expression, national origin, genetic information, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions, and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. WEP Clinical will make reasonable accommodation for qualified individuals with known disabilities, in accordance with applicable law.

Source

Posted by Wepclinical on their own hiring page, jobs.lever.co. OptiTalent shows it as published, read 07 Nov 2026 03:43 UTC; the original is the reference.

View the original ad ↗

More at Wepclinical

  • Responsible Person

    2 months ago

    Wepclinical · Dublin, Ireland

    On-siteFull-time

    The Responsible Person (RP) is an integral role within the company to ensure that EU Good Distribution Practice, national regulations, and provisions listed on the Wholesalers Distribution Authorisation are met and complied with at the company. The objective is to assure…

  • Wepclinical · Morrisville, North Carolina, United States

    HybridFull-timeSeniorEngineering

    The Site US Senior GMDP Quality Assurance Manager will provide senior leadership and accountability for the site quality assurance function supporting distribution and manufacturing activities, including secondary packaging and labelling. The role will oversee day-to-day site…

  • Wepclinical · Dublin, Ireland

    On-siteFull-timeManagerTrades & logistics

    The WEP Clinical cGMP Production Manager is responsible for both hands‑on execution and technical expertise of production, packaging, and labeling activities, ensuring compliant, efficient, and audit‑ready operations. The role oversees end‑to‑end GMP batch execution, including…

  • Wepclinical · United Kingdom

    RemoteMid level€1.00 an hourEngineering

    Job Description: As a Mobile Research Nurse, you will be crucial in ensuring the successful execution of research studies. You will be responsible for administering investigational medications/products, conducting patient assessments, collecting vital information, and adhering…