Validation engineer Role Athlone, Westmeath

CQV Engineer IV

  • Posted Mar 25, 2021
  • Athlone, Westmeath
  • Contract
  • VAC-19005

LSC have a great contract opportunity for a CQV Engineer to join a biopharmaceutical company based in Westmeath.

If you have 6 years+ relevant experience working in a Validation role in the Pharmaceutical / Biotechnology industry and are ready for your next challenge, this could be the perfect project for you!

o Validation documentation - drafting, reviewing and approving Validation documentation.
o Document coordinator support for Project and Sustaining operations
o Execute Temperature mapping studies for controlled temperature units and / or manufacturing areas.
o Participate in Validation Risk Assessments to determine the level of testing required for new equipment.
o Support sustaining and project Validation activities across Bulk Drug Substance, Packaging and Laboratory areas.
o Input into the core aspects of Operations, Qualification and Validation SOP's.
o Maintaining hardcopy records in Document control archive, including reconciliation of Document tracker.

o Technical Degree in Engineering/Life Sciences
o Experience of upstream / downstream drug substance processes would be an advantage

Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!

Apply via this advert or contact Conor Dolan at LSC on 021-4777329 if you have anymore questions about this CQV Engineer opportunity!

This could be the perfect project for you! Apply online and we’ll be in contact shortly


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The benefits of contracting with LSC

  • Partners to the world’s top Life Science companies we offer you the best contract opportunities in the industry
  • 95% of LSC contracts are renewed letting you choose contracting as a long term career option
  • LSC’s Consultant Success Programme focuses on skills development & on-site support to help you achieve your career goals!

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