Quality Assurance Officer

Location
Hertfordshire (GB)
Salary
Competitive salary and benefits
Posted
29 Jul 2021
Closes
17 Aug 2021
Ref
2907QAO
Discipline
Quality, QA / QC
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

DETAILS:

  • Full-time permanent position
  • Office based in Hertfordshire
  • Competitive package

 

THE ROLE:

  • Quality document review prior to QP release.
  • Generating BPRs for manufacturing.
  • Amending Manufacturing and Packaging master production records.
  • Reviewing & approving BOMs on SAGE.
  • Preparing batch release documentation, C of A and Batch Release Certificate.
  • Handling customer complaints and enquiries, including medical product information, coordinate technical product complaint investigations.
  • Handling and reporting of Adverse Drug Reactions / Adverse Events. Liaising with HPPV (third party Pharmacovigilance).
  • Product Quality Report preparation.
  • Raising and assessing deviations, change controls & CAPAs.
  • Artwork management including liaising with regulatory affairs and third party.
  • Controlled document management (versioning & database management).
  • Authoring and reviewing controlled documents (manufacturing logs, SOPs, etc.).
  • Raising purchase orders for artwork tasks and packaging materials.
  • Internal, external and customer audits.(Co-Auditor)

Full job description available on application

 

THE CANDIDATE:

  • Candidate MUST have at least 1 years experience in QA in the pharmaceutical industry within a GMP environment
  • Only candidates with existing right to work in the UK/EU will be considered

TO APPLY:

Please complete the details below to apply. For further information or a discreet discussion regarding your recruitment requirements, please call Alex on 01227 844466 or email alex@apexrecruitment.com

To view our other vacancies, please visit our website on www.apexrecruitment.com

Apex Recruitment are a specialist agency providing opportunities within the pharmaceutical, biopharma, biotech and medical device industries recruiting in the areas of medical affairs, drug safety, clinical and quality.