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Quality Specialist - GMP Quality - Pharmaceutical

  1. South East
  1. Contract
Competitive
23987WP
  1. Compliance / Quality Assurance
Date Posted03 Jan 2020

This vacancy has now expired

Would you be interested in joining a top 10 global Pharmaceutical client?
  • Long term contract assignment - 13months +
  • Excellent Glass door reviews & working environment!
We are looking for a QA Specialist to join the Quality department supporting the Quality /GMP activities. P
 
Duties will involve:
  • Completes review of data, procedures, facilities, equipment and systems (inc computer systems) to ensure compliance to SOPs, GMPs and applicable regulations.
  • Review and approve production & analytical documentation accompanying the release of drug substance, drug product and packaged finished goods to ensure conformance to appropriate SOPs, GMP and regulatory requirements
  • Resolve issues that arise during audit and review
  • Support product recalls and stock recoveries 
  • Identify compliance gaps and make recommendations for continuous improvement
  • Creates and maintains assigned SOPs.
  • Perform and review complaints and deviation investigations, change controls and CAPA’s.
  • Assist in the induction process for new starters

Skills Required
  • Degree in an Engineering or Science discipline
  • QA within a GMP environment
  • Review SOP's, GMP, data ensuring GMP compliant
  • Audit experience 
If this role is of interest, please apply now.



The candidate must have the rights to work in the location stated in the job advert.

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