Join a leading Biopharmaceutical company in Carlow, Ireland, as a Process Engineer on a dynamic contract opportunity. This cutting-edge vaccines and biologics manufacturing facility produces innovative products across various therapeutic areas including oncology, autoimmunity, pneumonia, and infectious disease.
About the Role
As a Process Engineer, you will lead and execute production floor-based activities, design and author process development studies, and provide technical input into quality notifications.
* Design and implement process development studies to support new product introductions and ongoing manufacturing support.
* Author and review qualification/validation documentation and studies in line with the standard approval process.
* Perform data analysis and make informed decisions/recommendations based on data-driven conclusions.
Your Background
We are seeking an individual with a Bachelor's Degree or higher in a Science, Engineering, or other technical discipline. Prior related work experience in manufacturing, preferably GMP, is ideal.
* Typically 3 years of relevant work experience in Aseptic manufacturing / process engineering.
* Familiarity with Fill Finish Drug Product Vial Filling, Syringe Filling processes.
What We Offer
This contract opportunity provides a chance to work with a global Biopharmaceutical leader, contributing to the development and delivery of life-changing products.