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QA Associate

Merseyside   •  Negotiable  •  Contract/Temporary, Full time


QA Associate

12 month contract

£23.66 per hour PAYE

Liverpool – On site

Cpl Life Sciences are recruiting for an experienced QA Associates to join a leading Pharmaceutical company based in Liverpool on a 12 month contract.

The main purpose of the QA Associate it to provide frontline QA support to the secondary operations.

Frontline/ shop floor QA experience is a necessity for this position.

Key Responsibilities include;

  • Providing cGMP and Quality support and guidance to the Secondary projects/operations (Filling, Inspection, and Packaging) and its support functions

· Perform QA Frontline duties during campaign operation of the Fill/Finish production lines (Filling, Inspection, Packaging), including technical and qualification batches as required

· Provide QA support to the wider business, as and when required by the Quality Assurance Manager

· Be responsible for QA review and approval of procedures, batch production records (master and executed), and any other relevant cGMP documentation

· Be confident in frontline quality decisions

· Support and perform tasks as required by the Quality Manager

· To ensure cGMP behaviours including aseptic behaviours are compliant

· Safeguard product quality and sterility assurance

· Provide support for deviation investigations, ensuring effecting root cause analysis investigations are performed

· Identify repeat deviations

· To ensure that deviations, CAPAs, protocols/reports and other applicable documents are reviewed and approved within the designated timelines

· To provide Quality oversight for manufacturing and support functions ensuring that appropriate standards of cGMP, housekeeping, Health, Safety and Environment are applied in the team and site areas of responsibility, in accordance with current regulations and procedures

Experience;

· Educated to graduate level

· Have excellent understanding of cGMP requirements

· Experience working in a pharmaceutical environment

· Experience working in secondary and or aseptic operations

· 2/3 years experience in Quality

· Understanding of EU and FDA regulatory requirements

Please apply here or contact Amy on amy.goddard@cpl.com

  • Agency: Cpl Life Sciences
  • Contact: Amy Goddard
  • Reference: JO-2108-474349
  • Updated: 9th September 2021
  • Expires: 7th October 2021

Cpl Life Sciences

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