LSC have a great contract opportunity for a Senior QC Associate to join a South Dublin based Biopharmaceutical company that specialises in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.
If you have 3-5 years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT – KEY RESPONSIBILITIES:
o Execute sample management activities across the site – sample distribution, LIMS logging
o Perform Stability Program related activities such as pulling stability samples, study initiations.
o Create/own and approve protocols, sample plans, SOPs, training manuals.
o Perform SAP, LIMS and CIMS functions/ transactions within the sample management remit
o Out of hours responder for sample management equipment (fridges /freezers / incubators)
o Responsible for their own training and safety compliance.
ABOUT YOU – ARE YOUR SKILLS A MATCH?
o Bachelor’s degree in a Science related field is required
o Experience with regulatory compliance in cGMP 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 1G/Stamp 4 visa to apply!
To apply, submit your CV via this advert or contact Aaron Kingston at LSC on 021-4777329 if you have anymore questions about this Senior QC Associate opportunity!