LSC have a great contract opportunity for a CSV Engineer to join a global Biopharmaceutical company in Carlow.
If you have minimum of minimum of 3 years’ experience in a similar role, ideally in the Pharmaceutical industry and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT – KEY RESPONSIBILITIES:
o The CSV engineer will be responsible for the development of key AIT quality documents, such as Quality Assurance (QAPs) and test plans, and for ensuing adherence to the QAPs.
o Develop and maintain Qualification Plans and Test Plans, aligned with the overall project C&Q plan and with the leveraging strategy.
o Develop templates for all SDLC deliverables, compliant with company standards, to ensure consistent implementation of the validation strategy, including but not limited to:
Requirements Traceability Matrix
Test specification/test script
o Work closely with the QAIT function and ensure their requirements are met in all deliverables
o Align with the company HPV program: leverage existing documents & expertise where feasible
o Approver of all AIT SDLC deliverables, ensuring compliance with standards
ABOUT YOU – ARE YOUR SKILLS A MATCH?
o Expert knowledge of GAMP5.
o Strong experience in one or all of the following systems: DeltaV, PCS7 (or other PLC/SCADA), OSI PI.
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 Paul O’Driscoll at LSC on 021-4777329 if you have anymore questions about this CSV Engineer opportunity!