LSC have a great contract opportunity for a Junior CQV Engineer (Utilities) to join a Dublin based Biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that can help patients overcome serious diseases and improve their quality of life.
If you have 2 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:- Support the Sterile Drug Product Facility project as part of the CQV team.
- Develop and execute commissioning and qualification plans for new and existing equipment and systems.
- Perform utility and system start-up activities, including functional testing and troubleshooting.
- Develop and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.
- Develop and execute validation protocols to support facility/utilities, equipment and computer systems validation.
- Ensure that validation activities comply with regulatory requirements (e.g., FDA, EMA, ICH) and industry standards (e.g., GAMP 5).
ABOUT YOU - ARE YOUR SKILLS A MATCH?- The candidate should hold a minimum of a BS qualification (Degree) in a scientific, technical, or engineering discipline.
- Previous CQV experience is an advantage, previous GMP experience is essential.
- Previous experience in working in a drug product filling facility would be advantageous.
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 Cian Marnane on 021 4777329 if you have any more questions about this role!
