About the Opportunity:
We are seeking a highly skilled Process Engineer to join our team in Carlow. This is an exciting opportunity to work in a state-of-the-art vaccines and biologics manufacturing facility that produces a range of products in various therapeutic areas.
About the Role:
* Design, author, review, approve, and execute qualification/validation documentation and process development studies in line with standard approval processes.
* Contribute to Kaizen events as required and provide technical input into quality notifications by authorizing/reviewing/approving investigations.
* Execute equipment/qualification validation programs, including re-qualification and re-validation, and support continuous improvement through Lean Six Sigma methodologies.
About You:
* You will hold a Bachelor's Degree or higher, ideally in a Science, Engineering, or other Technical discipline.
* You will have a minimum of 3 years' experience in manufacturing, preferably GMP.
* You will have demonstrable experience leading technical-related projects.
Requirements:
* Bachelor's Degree or higher in a relevant field.
* Minimum 3 years' experience in manufacturing, preferably GMP.
* Demonstrable experience leading technical-related projects.
Benefits:
* This is a contract opportunity, and you will need to hold a Stamp 1G/Stamp 4 visa to apply.
How to Apply:
Please apply via this advert or contact Adam Murphy for more information about this opportunity.