A permanent, full time position as a Quality Assurance Officer to oversee compliance with internal and GMP requirements has opened at a fast-growing manufacturing company based in North Lincolnshire, UK.
As part of a team responsible for maintenance and ongoing improvement of the quality management system, the ideal candidate would have experience in the following areas:
•Working in an EU GMP regulated environment.
•Preparation of quality documentation including, but not limited to; product quality reviews, stability study protocols, equipment and process qualification and validation.
•Performing audits – both internal and external.
•Documentation and investigation of Out of Specifications (OOSs) and deviations.
•Technical dossier authoring, with particular focus on CMC sections, including; stability trend analysis, analytical testing and validation, and justification of specifications.
•Review of batch documentation.
•Maintenance, review and documentation of company standard operating procedures.
This position would suit a quality professional with 3 - 5 years’ experience within a highly regulated environment, either from an FMCG, food or pharmaceutical background and who, having gained some experience, now wishes to assume more responsibility within the quality department.
The ideal candidate would be educated to degree level in a relevant scientific discipline, have an analytical mind, excellent computer skills and the ability to work within small cross-functional teams.
The remuneration package will be based on experience and qualifications of the candidate.
Please send your CV and covering letter addressed to Rachel Watson at firstname.lastname@example.org