Validation Engineer Role Denmark

Validation Engineer

  • Posted Jun 26, 2024
  • Denmark
  • Contract
  • BBBH27666

LSC has a fantastic opportunity for a Validation Engineer to join an advanced global team in Denmark that promotes self-development, encourages collaboration, and fosters a learning environment. This is a chance for you to be a part of a fast-growing, multicultural company that has a compelling vision for shaping the future of medicine.

ABOUT THE PROJECT - KEY RESPONSIBILITIES:

  • Perform PQ activities primarily on downstream process equipment.
  • Write, review, approve validation documents.
  • Execute testing, data evaluation and reporting.


ABOUT YOU - ARE YOUR SKILLS A MATCH?

  • 3-5 years' experience in performing and document qualification and validation.
  • 2-3 years of relevant industry experience from biological drug substance manufacturing.
  • Experience with PQ execution preferably from downstream equipment and Cleaning Validation.
  • Familiar with risk Based Qualification and Kneat (Electronic Validation system).
  • Familiar with performing the following types of test: Clean hold, Mixing validation, Microbial hold.


Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold an EU/UK Passport to apply! Apply via this advert or contact Sarah Ninan at +353 214777329 if you have any more questions about this opportunity!

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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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