Apex International Recruitment Ltd

* Full-time permanent position

* Office based in Hertfordshire

* Competitive package


* 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


* 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*


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

To view our other vacancies, please visit our website on

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.

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