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 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!
Apply via this advert or contact Caoimhe O Sullivan on 021 4777329 if you have anymore questions about this role!
