LSC have a great contract opportunity for a LIMS Project Analyst to join a Bray based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.
If you have 1+ years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect project for you!
About the role: The LIMS Project Analyst is responsible for ensuring that the effective deployment of LIMS Labware V8 at TILGC, aligned with industry best practices and to meet local expectations.
This includes proactively developing, implementing, LIMS Master data to support manufacture, testing, and release of products.
Key Responsibilities: Configuration or modification of LIMS setups, including microbiology or QC Analytical methods, product specifications, schedulers, standards & reagents, COA's, Label and printer setup, and associated LIMS Master Data.
* Creation and verification of LIMS Master Data as required.
* Development of Test Scripts/Test Protocols for formal LIMS test execution as required.
* Execution of informal and formal verification testing of the configured LIMS solution in collaboration with Computer Systems Validation (CSV) project resources.
Requirements * Bachelor's degree in a life sciences, IT or a related scientific discipline.
A minimum of 1 years LIMs administration / Master Data Building.
* Experience working in finished product pharmaceuticals/biologics, including analytical chemistry, quality assurance, quality control, development, and/or manufacturing areas.
* Thorough understanding of quality systems and cGMP's.
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 Kieran McCarthy on if you have any more questions about this opportunity!
Skills: LIMS GMP cGMP Master Data Building