Establishing a long-term relationship with LSC as a Process Engineer presents an exceptional opportunity to contribute to the success of a leading global Biopharmaceutical company in Carlow.
This state-of-the-art vaccines and biologics manufacturing facility is currently producing products across various therapeutic areas, including oncology, autoimmunity, pneumonia, and infectious disease.
About the Role
* Design, author, review, approve, and execute qualification/validation documentation and process development studies in line with standard approval processes.
* Develop and implement change controls, contributing to Kaizen events as necessary.
* Provide technical input into quality notifications by authoring, reviewing, and approving investigations.
* Execute equipment/qualification validation programs, including re-qualification and re-validation.
* Support continuous improvement through Lean Six Sigma methodologies.
About You
* Bachelor's degree or higher required, ideally in a Science, Engineering, or Technical discipline.
* Preferably one year's experience in manufacturing, preferably GMP.
* Previous experience with Automated Visual Inspection Systems is desired but not essential.
Please note that you must be eligible to work in Ireland, holding a Stamp 1 G/Stamp 4 visa to apply. If you have any questions about this opportunity, please contact Adam Murphy. Required skills include inspection, filling, change control.