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Have you got what it takes to succeed The following information should be read carefully by all candidates.
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! xcfaprz Apply via this advert or contact Caoimhe O Sullivan on if you have anymore questions about this role! Skills: Quality Control Quality Senior Systems configuration Pharmaceuticals Manufacturing
Sprachkenntnisse
- English
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