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/Execute 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.
- Preferably Min 2 years' experience ideally in manufacturing, preferably GMP Setting
- Equipment and process validation
- Sterile filling processes and equipment
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 Sarah Ninan at 0214777329 if you have any more questions about this opportunity!
