Quality Assurance Role Dublin

Quality Specialist

  • Posted Mar 23, 2021
  • Dublin
  • Contract
  • VAC-18871

LSC have an exciting contract opportunity for a Quality Specialist to join a leading Biotech company based in Dublin.

If you have a minimum 3-5 years pharmaceutical and/or biotech industry experience in Quality/ Compliance / Validation related role and are ready for your next challenge, this could be the perfect project for you!

ABOUT THE PROJECT - KEY RESPONSIBILITIES:
o Lead the QRM activities required for the NPI capital projects
o Act as QRM facilitator and Risk lead for project QRAs
o Schedule the completion of project QRAs and track to completion including tracking to closure associated QRM CAPAs
o Ensure linkage from the output of the QRAs to the Commissioning, Qualification and Validation strategies
o Support the facilitation of site QRAs which are required for update as a result of NPI
o Present QRAs for concurrence at Site QRM Council

ABOUT YOU - ARE YOUR SKILLS A MATCH?
o Degree in natural or applied sciences (Biotechnology, Pharmacy, Biology, Engineering)
o Experience in startup biotechnology and drug substance facilities a distinct advantage
o Familiarity with Commissioning & Qualification lifecycle deliverables

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 Katie Brown at LSC on 021-4777329 if you have anymore questions about this Quality Specialist opportunity!

This could be the perfect project for you! Submit your CV below 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
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