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Quality Control Officer

Reed
Posted 15 hours ago, valid for 16 days
Location

Runcorn, Cheshire WA7 2FG, England

Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • The Shift Quality Control Officer position is based in Runcorn and offers a permanent role with a salary of £30,000 plus a £4,500 shift allowance.
  • The company is a global pharmaceutical manufacturer specializing in biopharmaceuticals, medical nutrition, and I.V. drugs, aimed at aiding critically ill patients.
  • The role involves approving batches for market release, reviewing documentation, and supporting investigations related to product quality and compliance.
  • Candidates should ideally have a degree in a life science subject or relevant experience in quality assurance within a regulated environment, with sterile manufacturing experience being highly desirable.
  • The position requires knowledge of GMP standards, specifically for sterile manufacturing as outlined in the MHRA Orange Guide.

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.

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.