LSC have a great contract opportunity for a Quality Control 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 3 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:
- Participate in process engineering activities.
Facilitate the development of new business SOPs, Forms, Manuals, etc. using new processes/workflows. - Participate in system requirement, software configuration, and design activities.
- Receive and/or verify master data for the site(s).
- Coordinate ELN Template development and review with site SMEs.
- Support the development and review of Operational Qualifications.
- Execute User Acceptance Testing & Data Migration Verification.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Bachelor's degree and 3 years of industry Quality Control or Quality experience.
- GxP experience, specifically practices and requirements in the testing of biopharmaceuticals.
- Experience in development and validation testing of software used in a GMP environment.
- Experience and knowledge in using electronic lab notebook systems and inventory management systems (Biovia OneLab, ThermoFisher Sample Manager, LabWare, Benchling, etc.).
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!
