LSC have a great contract opportunity for a Junior CQV Engineer (Equipment) 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:
- Generating and completing CQV documentation to satisfy requirements and executing test deliverables for requalification and periodic review testing as applicable.
- Adhering to deadlines as scheduled by the team leader.
- Inputting to a wider CQV team and liaising with cross-functional teams to ensure timely completion and approval of CQV deliverables.
- Investigation support using QMS (Quality Management Systems) and troubleshooting for CQV issues.
- Ensuring adherence to governing site and global procedures and regulatory guidelines.
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.
- The ideal candidate would have biopharmaceutical Process / Validation knowledge.
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!
