We are seeking a skilled Process Engineer to contribute to the success of our global Biopharmaceutical organization.
Key Responsibilities:
* Develop and execute qualification/validation documentation and process development studies in line with industry standards.
* Design and implement change controls, contributing to Kaizen events as necessary.
* Provide technical input into quality notifications by authoring, reviewing, and approving investigations.
* Lead 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 preferred, ideally in a Science, Engineering, or Technical discipline.
* At least 3 years' experience in manufacturing, preferably in a GMP setting.
* Demonstratable experience leading technical-related projects.
Requirements:
* Eligibility to work in Ireland; Stamp 1 G/Stamp 4 visa required for contract opportunities.
Why Choose This Role?
* Work in a state-of-the-art vaccines and biologics manufacturing facility.
* Opportunity to develop your skills and advance your career.
* Possibility to work on exciting projects that drive business growth.