Validation Engineer

3 weeks ago

Cork, Cork, Ireland ARTO Full time

We have partnered with a Global Medical Device company based in Cork, Ireland. They are searching for a strong Validation/Manufacturing Engineer to support a site expansion, introducing new production lines and equipment (new cleaning lines/equipment).

Responsibilities
  • Validate cleaning equipment/lines in the Medical Device or Pharma setting.
  • Decommission and commission new production lines from scratch (URS, FAT, SAT, IQ, OQ, PQ).
  • Manage the delivery of full end-to-end projects from a Validation standpoint.
Qualifications
  • Experience validating cleaning equipment/lines in the Medical Device or Pharma setting.
  • Hands-on experience decommissioning and commissioning new production lines from scratch (URS, FAT, SAT, IQ, OQ, PQ).
  • Proven track record delivering full end-to-end validation projects.
Contract details
  • Initial contract duration of 12 months with potential extension to 2–3 years.
  • Estimated start date ideally October.
Seniority

Mid-Senior level

Employment type

Contract

Job function
  • Engineering and Manufacturing
Industries
  • Medical Equipment Manufacturing
  • Pharmaceutical Manufacturing
  • Biotechnology Research

Note: This description excludes non-job-related content and extraneous postings to focus on the responsibilities and requirements for the role.


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