Quality Systems Manager

As the Quality Assurance Manager you will be responsible for:
* Ensuring cGMP/GDP compliance of imported products according to the approved licences and EU requirements.
* Coordinating for batch testing and QP release of imported batches.
* Generation, review and control of documents like SOPs, Change control, deviation, Internal and external Audits, staff training, temperature control documents.
* Approval of pre-production documents viz. batch documents, stability & validation protocol.
* Specification for new customers and new products coming in.
* Artwork approval, post production documents review for MHRA variation and for QP release.
* Annual product review, managing technical agreements. Handling of market complaints, handling of regulatory and customer audits.
* Managing the audits of warehouse, QC testing labs manufacturing sites, API's and excipients.

To be eligible to apply you must:
* Hold a degree in Analytical science or Chemical Science
* Direct Experience of cGMP Pharmaceutical Manufacturing
* Have extensive experience of MHRA, FDA Regulatory Authorities
* Show excellent communication skills

The role offers an excellent starting salary and benefits structure. If you are interested in this fantastic opportunity please email an updated CV to John Morkus Head of Quality Recruitment or call 0207 758 7311, the role is based in West London easily commutable from Buckinghamshire, Slough or Uxbridge.

Keywords: Quality Assurance Manager, Manage Head of Quality, Quality Assurance, QA, Internal Audit, External Audit, Quality Systems, Quality Management Systems, QMS, Compliance,API, Responsible Person.

To find out more about Real Staffing please visit www.realstaffing.com