LSC have a great contract opportunity for a QA Validation – Clean Hold to join an innovative and rapidly growing Biopharmaceutical company in Limerick.
If you are experienced in QA Validation activities and have experience on writing and approving Deviations/ GMP documents and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT – KEY RESPONSIBILITIES:
o Taking Clean hold rinse and swab samples on process equipment and small parts
o Working closely with manufacturing to ensure the CIP/SIP and holds are achieved and samples are taken.
o Working with engineering to determine flow paths for rinse samples and surface area calculations
o Shows focus & a consistence approach to the role and tasks.
o Generating and Executing Validation Protocols.
o Actively look for Continuous improvements
o Generate/review/Approval of CV protocols
o Generate Reports
ABOUT YOU – ARE YOUR SKILLS A MATCH?
o Experience in aseptic technique
o Experience in Gowning for ISO8
o Technical writing experience in writing site reports.
o Experience in Validation specifically cleaning/ clean validation
o Experience in assessment of cleaning issues during study runs
o Experience in Deviation/Change control writing
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!
To apply, submit your CV via this advert or contact Kathy Gillen at LSC on 021-4777329 if you have anymore questions about this QA Validation – Clean Hold opportunity!