Principal Validation Specialist

  • Location

    Holmes Chapel, Cheshire

  • Sector:

    Engineering

  • Job type:

    Contract

  • Salary:

    £45000 - £50000 per annum + + Benefits

  • Contact:

    Sarah Kesaulija

  • Contact email:

    Sarah.Kesaulija@experis.co.uk

  • Job ref:

    BBBH119455_1582711826

  • Published:

    8 months ago

  • Duration:

    12 Month FTC

  • Expiry date:

    2020-03-27

Principal Validation Specialist- £45,000-50,000 - Cheshire

A leading Pharmaceutical Manufacturer based in Cheshire are seeking an experienced Validation Specialist for a 12 Month Fixed Term Contract.

We will be looking for the individual to be able to develop and execute qualification & validation protocols. The Principal Validation Specialist will also generate reports to support the implementation of site projects.

This is a great opportunity to join a leading manufacturing organisation in the North West who are deemed as experts within the Validation world.

Whats on offer?

  • Salary up to £50,000
  • Great career progression working for a leading Pharma Manufacturer
  • Generous benefits package

Major Responsibilities / Accountabilities:

  • Developing validation master plans, protocols, reports and to generate related summary reports
  • Support site engineering project managers in developing and reviewing and approving URS documents, specifications, assessments, acceptance criteria and test/inspection requirements and any other related validation procedures
  • Assist in pre-qualification commissioning activities
  • Execute installation, operational and performance qualification protocols and related documentation.
  • Ownership of any related Q&V deviations to resolution and closure
  • Owning, initiating and updating as required Q&V related change controls, events, CAPAs and improvement actions

Qualification/ Skills & Attributes:

  • Knowledge of HSE within a Pharmaceutical organisation
  • Life Sciences degree is beneficial
  • 3-5 Years minimum experience of working within Validation
  • Technical writing experience
  • Compliance & regulatory background within pharma

If you would like to be considered for the position please submit an application or contact Sarah Kesaulija on 01179 309 708