LSC have a great contract opportunity for a QA IT Specialist to join a global Biopharmaceutical company in Carlow.
If you have minimum 5 years in QA IT/CSV, CSV, lab instrumentation experience on Large Scale Projects and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
o Providing independent quality review and approval of system lifecycle documentation, such as plans, requirements, risk assessments, protocols and reports for new and modified systems.
o Providing independent quality review and approval of system changes.
o Supporting and approving computerised systems investigations and test deviations.
o Ensuring consistent approach to qualification, change and deviation management across systems being implemented on the project.
o Providing timely and pro-active QA IT support and guidance to facilitate project timelines, including close collaboration with the technical and business units.
o Where required, engaging with QA IT teams from other sites and capital projects to standardise and align approach to computerised systems compliance
ABOUT YOU - ARE YOUR SKILLS A MATCH?
o Min. 5 years of experience in QA IT/CSV, CSV, lab instrumentation and/or a similar role in the pharmaceutical industry.
o Working knowledge of relevant regulations and industry standards.
o Proven ability to meet timelines, prioritise tasks and engage with stakeholders.
o Excellent communication skills.
o Project management experience will be an advantage.
o Analytical systems experience is essential.
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 LSC on 021-4777329 if you have anymore questions about this QA IT Specialist opportunity!