LSC have a great contract opportunity for a Quality Engineer (Senior) to join a South Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- QMS and maintaining it in an "Audit Ready" state.
- Creation and execution of FAT, commissioning & SAT protocols.
- * Responsible for the creation of validation exercise documentation including validation protocol (DQ, IQ,OQ,PQ) and master validation plan.
- Preparation of package turnover over documentation.
- Take responsibility for being quality gateway for your own deliverables.
- Line review and verification against the Master Validation Plan(MVP) to ensure all validation activities are properly and completely documented and updating of the MVP in a timely manner such as when there are new validation activities and changes to existing validation.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Bachelor's Degree in Mechanical, Mechatronic/Electromechanical or equivalent years of related experience.
- Minimum of 2-5 years of working experience in Medical related field.
- Experience in Computerized System Validation will be an added advantage.
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 Adam Murphy on 021 4777329 if you have anymore questions about this role!
