Posted to MedZilla on 8/21/2017


England, Quality Consultant QA_JE_13143-MZ


ProClinical is currently seeking a Consultant to work on a large complex medical Device project in Cambridge. The position supports quality assurance activities related to quality system compliance and continuous improvement. The ideal candidate will have a Quality Assurance background in an in vitro diagnostic or molecular reagent company and/or a product development background in molecular biology products or molecular diagnostic products company utilizing nucleic acid technology. It's an initial 6-month contract but with a very high chance of extension.

Job Responsibilities

  • Manage or support the document control program as well as suggest and implement improvements to existing process.
  • Support the training program as well as suggest and implement improvements to existing process.
  • General support and may assist in the investigation and resolution of nonconforming events and CAPA projects.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Joseph Emmott on +44 203 8141 316 or upload your CV on our website -
A full job description is available on request.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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* If a direct employer requests that you go to their web site and complete your application there in order to be
  considered, please do so. Applications for all positions are subject to each employer's specific requirements.