LSC have a great contract opportunity for a Process Engineer to join a global Biopharmaceutical company in Carlow. This is a state-of-the-art vaccines and biologics manufacturing facility currently producing many products in various therapeutic areas including: oncology, autoimmunity, pneumonia, and infectious disease.
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
* Design/Author/Review/Approve/Execute qualification/validation documentation and process development studies in line with the standard approval process
* Design/Author/Review/Approve/Execution/development of change controls
* Contribution to Kaizen events as appropriate
* Technical input into quality notification by authoring/reviewing/approving investigations
* Execution of equipment/qualification validation programs; including re-qualification and re-validation
* Support continuous improvement through Lean Six Sigma methodologies
ABOUT YOU - ARE YOUR SKILLS A MATCH?
* Bachelor's Degree or higher preferred; ideally in a Science, Engineering or other Technical discipline
* Min 3 years' experience ideally in manufacturing, preferably GMP Setting
* Demonstratable experience of leading technical related projects
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 at if you have any more questions about this opportunity