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Quality Assurance Specialist
An interesting role has become available as a Quality Assurance Specialist based in North Manchester. As the Quality Assurance Specialist, you will be responsible for up-keep and compliance of the QMS, overseeing internal company processes to ensure the business is always GMP and GDP complaint.
Responsibilities for the Quality Assurance Specialist
- Technical Document witing, SOPs, Deviations, non-conformance/ non compliances, and other similar Quality Assurance documents.
- Review of Batch manufacturing records, prior to QP release.
- Management and data entry for the QMS for, Change Controls, CAPAs and Non-Conformances.
- Assistant with continuous improvement and development of the QMS.
- Management of customer complaints, change controls, route cause analysis, and provide solutions to the matter.
- Contact with Suppliers to ensure Quality Assurance compliance- EG leaflets.
- Participate and provide support for both internal and external audits.
- Communication with multiple departments to improve Quality and improve daily operations.
- Provide training activities and maintain records for quality training within the business, personal and team members.
Requirements for the Quality Assurance Specialist
- Hold a relevant scientific degree.
- 3 years' experience working within a pharmaceutical company, within Quality Assurance.
- Excellent organisation and communication skills
- Strong knowledge of pharmaceutical GMP.
Benefits for the Quality Assurance Specialist
- Free parking
- Social working hours
- No weekend work
- Good career development opportunities
Please apply now to be considered or contact Liam Shannon at Smart4Sciences on
