LSC have an exciting contract opportunity for a QA Validation Specialist to join a leading Biotech company based in Dublin.
If you have of 3 years experience in, Quality Assurance,Technical Operations or Engineering within the Biopharma / Pharmceutical industry and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT – KEY RESPONSIBILITIES:
o Act as Quality Assurance approver for qualification/validation lifecycle documents.
o Serve as a quality assurance resource for assessing validation requirements, non-conformance, impact assessments, root cause analysis and implementation of CAPA found during CQV activities.
o Will serve as the Quality SME for all validation activities across the site including but not limited to Steam in Place(SIP), Cleaning Validation & CTU (Controlled temperature Unit) Performance qualification
o Provide Quality Assurance Validation support for Steam In Place (SIP) of buffer and media preparation systems, upstream (bioreactors) and downstream equipment trains & Autoclave loads.
ABOUT YOU – ARE YOUR SKILLS A MATCH?
o Bachelor’s degree (or higher) in Engineering, Chemistry, Biology, or relevant discipline, the successful candidate will also ideally have a proven track record in delivering excellence.
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 Conor Dolan at LSC on 021-4777329 if you have anymore questions about this QA Validation Specialist opportunity!