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QC Validation Specialist

  1. North West
  1. Contract
Competitive
24696
  1. Commisions, Qualification and Validation
Date Posted16 Apr 2020

This vacancy has now expired

QC Validation Specialist - Global Pharmaceutical Client – 12 Month Contract in North West, UK

Our client that specialises in the treatment and prevention of serious human medical conditions is currently seeking the expertise of an QC Validation Specialist to help with the set up of a new laboratory on their site in the North West.

Essential Duties and Responsibilities for this role include, but are not limited to, the following:

  • Leading and performing small to medium size validation activities including improvement activities and major projects (including time and cost planning) whilst ensuring that resources, raw materials and documentation are available to facilitate the smooth running of validation activities
  • Planning and prioritising own workload to ensure agreed deadlines are met including:
    • Coordinating and performing validation activities
    • Tracking and reporting the progress of these activities to validation, QA and process leaders
    • Managing project team resources and priorities and anticipating and removing obstacles to progress
  • Maintaining validated status by fulfilling re-validation and re-evaluation commitments and be responsible for VMP maintenance in nominated areas. Provide technical leadership on validation issues and resolve both GMP and business issues and deviations
  • Creating, executing, reporting validation documentation to meet regulatory and company standards. Support Operational Excellent Initiatives. Demonstrate company values and behaviours within their work.
  • Have knowledge of key validation and GMP requirements
Requirements:
  • Educated to graduate level in a scientific discipline or equivalent
  • Strong cGMP background in the Biological or Pharmaceutical industry
  • Experience of sterile manufacturing
  • Have experience in the validation of QC Laboratory equipment. Preference for knowledge in the validation QC facilities and utilities. Previous experience of QC equipment validation is required.
  • Previous experience of generating and executing IQ, OQ, PQ on GMP equipment.
  • Exposure to CSV and IT systems is desirable.
  • Experience of QC testing techniques and industry practices is desirable, to include Biological and Chemistry testing
If you are interested in this role, please apply now for more information!




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

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