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!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
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.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
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!
