Quality Specialist job in Hertfordshire, England

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Job type: Contract

Discipline: Good Manufacturing Practice (GMP)

Location: United Kingdom

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.

Responsibilities:

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.

#QACompliance

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