Technical Writer Role Limerick

QA Validation - Technical Writer

  • Posted Jun 1, 2022
  • Limerick
  • Contract
  • BBBH6879

LSC have a great contract opportunity for a QA Validation - Technical Writer to join an innovative and rapidly growing Biopharmaceutical company in Limerick. The facility is responsible for the production, packaging, labelling and delivery of biopharmaceutical medicines for global markets. The company currently markets medicines for various diseases and has a rich pipeline of products.

If you have experience in QA Validation activities and are ready for your next challenge, this could be the perfect project for you!


  • Experienced Technical writer o Experience in Deviation and investigation writing
  • Experience in Validation specifically CIP/SIP and continuing validation
  • Experience in assessment of CIP/SIP issues during study runs and closeout of deviations
  • Experience in KAYE validator reporting review beneficial
  • Capable of managing a large program, so project management skills would be necessary
  • An understanding of how manufacturing, CIP and SIP Validation equipment works


  • Execution, review & approval of SIP/ CIP and continuing validation protocols and closure
  • Extensive experience on writing and approving Deviations

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 Sarah Ninan if you have any more questions about this XXXXX 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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