Quality Specialist

Highly Competitive
  1. Contract
  2. Good Manufacturing Practice (GMP)
  3. United Kingdom
Hertfordshire, England
Posting date: 04 Dec 2023

This vacancy has now expired. Please see similar roles below...

Proclinical are recruiting for a Quality Specialist to join a pharmaceutical organisation. This role is on a contract basis and is located in the UK.


  • Responsible for document management, which involves SOP evaluation, drafting and finalisation, CAPA management and metric management.
  • Offer service provider oversight as well as GxP training compliance.
  • Handle quality risk management as well as annual product quality evaluation.
  • Support the preparations and performance of GxP audits and take charge of inspection actions.
  • Partake in the preparation, validation and drafting of QMS quality reports and affiliated preparation for QMS management evaluations.
  • Conduct trends analysis on QMS KPIs for evaluation and agreement of LQR/QP.
  • You will offer aid on any quality, QMS and medical compliance special projects.
  • Assist upholding the SOP training grid, always guaranteeing GxP training compliance across conglomerate.
  • Other duties may be assigned to this role.

If you are having difficulty in applying or if you have any questions, please contact Will Hitchcock at +44 203 0789 554.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.