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Quality Control Officer

Reed Specialist Recruitment
Posted 7 hours ago, valid for 16 days
Location

Runcorn, Cheshire WA7 1BE, England

Salary

£30,000 - £4,500 per annum

Contract type

Full Time

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Sonic Summary

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  • The Shift Quality Control Officer position is available in Runcorn with a permanent contract offering a salary of £30,000 plus a £4,500 shift allowance.
  • The role involves approving batches for market release, reviewing documentation, and supporting investigations related to product quality and compliance.
  • Candidates should have a degree in a life science or relevant experience in quality assurance within a regulated environment such as pharmaceuticals or medical devices.
  • Experience in a sterile manufacturing environment and knowledge of GMP requirements is highly desirable.
  • Interested applicants can contact Dave Cattell at Reed for more information or apply directly.

Shift Quality Control Officer (Earlies and Lates)

Runcorn

Permanent

30,000 + 4,500 Shift Allowance

The Company

Our client is a Global Pharmaceutical Manufacturer of biopharmaceuticals, biosimilars, medical nutrition, medical devices and I.V. drugs. The company's products and services are used to help care for critically and chronically ill patients in areas such as Oncology, antibacterials, anaesthesia and rheumatoid arthritis to name a few.

The role

Reporting to the QC Shift Team Leader, the QC Officer will be performing a range of duties in accordance with cGMP standards including:

  • Approving individual batches for release to market or further internal use
  • Reviewing batch documentation as part of the product release process
  • Supporting investigations of non-conformities that may impact upon the release process, product quality or compliance of the ASU facility
  • Compiling Certificates of Conformance as required
  • Liaising with other departments to ensure that the requirements of the QMS are met

Qualifications

To succeed in this role suitable applicants should ideally have a degree or equivalent in a life science subject or be able to demonstrate experience of working in a quality assurance or control related function within a highly regulated environment (eg Pharmaceutical, Chemical, Biotech or Medical Device industry)
Experience of working in a sterile manufacturing environment would be highly desirable as would a demonstrable working knowledge of GMP requirements specifically for sterile manufacturing as defined in the MHRA Orange Guide

To find out more about this role please contact Dave Cattell at Reed or apply below.

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By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.