Role Description

This is a full-time on-site/hybrid role for a Manager of Quality Services based in our stunning headquarters in Hartley Wintney, Hampshire. As a Manager of Quality Services, you will be a key member of the TMC in-house team reporting to the Associate Director of Quality Assurance. This role is responsible for managing TMC’s Quality Management System, for providing QA guidance and oversight to the TMC team and Clients, Hosting Client audits, supporting the delivery of TMCs Internal and Vendor Audit Program and for QI and CAPA management.

You will get the opportunity to work on a wide range of quality activities in some very interesting disease/treatment areas, and to further develop your skills.

Qualifications and Experience

  • Strong knowledge of ICH GCP and relevant regulations (EMA, MHRA).
  • GCP certification within the last 2 years
  • Minimum of 5 years prior experience in an Audit/QA function of the Pharmaceutical/pharmaceutical service Industry
  • Familiarity with quality systems
  • Other GxP knowledge and experience would be desirable
  • Experience of Process Management (authoring, reviewing, approving SOPs and associated controlled documents) would be of benefit
  • Experience of FDA regulatory environment desirable
  • Experience of requirements of MAH/GMP desirable
  • Excellent analytical and problem-solving skills
  • Ability to work effectively in cross-functional teams
  • Exceptional attention to detail
  • Excellent written and verbal communication skills
  • Strong organisational and time management skills
  • Bachelor’s degree in a related field
  • Advanced degree in a related field is a plus

Employment Type

Full-time