LSC have a great contract opportunity for a QC Senior Associate to join a South Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.
If you have 5 years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you! ABOUT THE PROJECT - KEY RESPONSIBILITIES: Execute sample management activities across the site - sample distribution, LIMS logging, shipment receipt Perform Stability Program related activities such as pulling stability samples, study initiations.
Create/own and approve protocols, sample plans., SOPs, training manuals.
Perform SAP, LIMS and CIMS functions/ transactions within the sample management remit ABOUT YOU - ARE YOUR SKILLS A MATCH? Bachelor's degree in a Science related field is required.
5+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry, where 2 - 3 years of specific sample management/ stability programme experience is desirable.
Experience with regulatory compliance in c GMP manufacturing and testing of pharmaceutical products.
Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1 G/Stamp 4 visa to apply! Apply via this advert or contact Caoimhe O Sullivan on if you have anymore questions about this role! Skills: QC Senior LIMS