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QAV Engineer

  1. South East
  1. Contract
Competitive
24848/ZM
  1. Life Sciences
Date Posted21 May 2020
QAV Engineer - Global Pharmaceutical Organisation - South East England

We have an exciting opportunity for an experienced QA Validation Engineer to join a large new project for a global pharmaceutical organisation, in The South East of England with great longevity of employment possibility.

DUE TO TRAVEL RESTRICTIONS CAUSED BY THE CORONAVIRUS WE CAN ONLY ACCEPT APPLICATIONS FROM THOSE RESIDING IN The UK AT THIS TIME.

Who are we looking for?

Act on behalf of QA interfacing with the project delivery team. Prepare/review key validation documents including; validation plans, risk assessments and traceability matrices. Support projects to ensure validation documents (e.g. DQ, IQ, OQ, PQ, PV, URS’s, traceability matrices and risk assessments) are produced at the appropriate time to maintain compliance and avoid delays in projects. Ensure the documents are of an appropriate standard to demonstrate compliance and are aligned to developing industry trends in validation strategies. Act as validation approval on commissioning and validation documentation. Execute protocols as required by projects. Witness execution testing as required. Periodic reviews, Equipment history files, Documentation management, Change controls.

The ideal candidate will have:

Education to degree standard, preferably in scientific or quality systems discipline or experience from vocational training

Relevant experience in a QA validation role in the pharmaceutical industry

Knowledge of Quality Systems including technical investigations (complaints, OOS, deviations, failure investigations, validation, etc.) and auditing

Previous experience of overseeing execution and reviewing/drafting IQ,OQ,PQ and URS’s.

Ideally project based experience with exposure to primary manufacturing operations (extraction) as well as Drug Product operations. (cappers, fillers and packaging)

Excellent interpersonal skills and the ability to work as part of a team or independently to agreed deadlines

Excellent attention to detail

For more information on this project / position, please apply with a copy of your up to date CV today! 

The candidate must have the rights to work in the location stated in the job advert.

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