LSC have a great contract opportunity for a C&Q Engineer to join a Cork based Biopharmaceutical company.
The site manufactures low volume bulk API for Phase III clinical trials, initial product launch and long-term market support.
The team on site grow, purify, formulate, and bulk fill mammalian cell culture derived APIs for medicines intended for human use.
If you have 5 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: Co-ordination/Execution of Protocols to meet project schedules etc.
Ability to manage workload of multiple projects of varying complexity.
Generation of System Traceability Matrices, C&Q Risk Assessments, C&Q plans, test cases and reports Experience in writing protocols, traceability matrix's, DQ's.
The engineer needs to have brought a project through commissioning/DQ/IOQ/RTM life cycle.
Document generation and execution for assigned systems (FAT, SAT, RV, IV, OV).
ABOUT YOU - ARE YOUR SKILLS A MATCH?
A BEng or BSc degree is preferred 5 years + experience in C&Q on projects in the Pharmaceutical/Biotechnology industry Experience in Packaging is desirable.
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 at LSC on if you have any more questions about this role!
Skills: Commissioning Qualification Validation