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Pharmaceutical Cleaning Validation Lead

Pharmaceutical Cleaning Validation Lead

Job Title: Pharmaceutical Cleaning Validation Lead
Contract Type: Permanent
Location: Cambridge, Cambridgeshire
Industry:
Salary: £45000 - £50000 per annum
Reference: HQ00055344_1492074206
Contact Name: Rachel Radford
Contact Email: r.radford@sciproglobal.com
Job Published: April 13, 2017 10:03

Job Description

My client, a pharmaceutical company based in Cambridge, are currently recruiting for a Cleaning Validation Lead to join their team as part of the Manufacturing Operations Support Group.

The primary function of this role is to plan, coordinate and execute Production facility/equipment Cleaning Validation/Verification activities ensuring full compliance and absence of cross-contamination between product manufacturing.

Key responsibilities:

  • Act as the key Point of Contact (POC) to handle daily activities related to Cleaning Validation and/or Verification.
  • To ensure that new products, processes and equipment are appropriately assessed and the necessary activities are carried out in support of cleaning validation or verification needs.
  • Generate cleaning verification/validation protocols and submit for approval.
  • Review and/or approve CV related documents, such as protocol(s), deviations, and summary reports.
  • Execute CV protocols and ensure all further actions, as applicable, are resolved adequately and summarised accordingly to attain post-execution protocol approval.
  • To organise and chair regular CV meetings
  • Conduct CV training/sessions if required.
  • Plan, co-ordinate and execute appropriate equipment CV related tasks to ensure that process equipment is adequately validated for commercial use.
  • Perform necessary equipment/product assessments in order to determine the scope of CV required.
  • Develop the appropriate documentation to capture equipment product contact surface areas; materials of construction; swab points/sites in collaboration with relevant support functions.
  • Generate, review and/or approve CV related documents, such as cleaning verification/validation protocols deviations, and summary reports.
  • Execute CV protocols and ensure all further actions, as applicable, are resolved adequately and summarised accordingly to attain post-execution protocol approval.

Key requirements:

  • Relevant scientific qualification desirable
  • Interacts with other functions in order to ensure timely delivery of projects.
  • Will have a demonstrated track record with relevant experience working in a regulated industry preferably in Pharmaceuticals.
  • Good oral, written and presentation skills essential
  • Focus on delivery.
  • Good team player.
  • Able to work effectively within a team or on own.
  • Approachable and willing to assist team/colleagues where required

If this sounds like something you would be interested in discussing further, please don't hesitate to apply!