Automation Process Engineer – Pharmaceutical Industry
Location: Co. Waterford | Contract: 12 months (with extension) |
About the Role
An opportunity has arisen for an experienced Automation Process Engineer to join a well-established pharmaceutical company in Co. Waterford. This role focuses on the implementation and optimization of Automated Visual Inspection (AVI) processes for pre-filled syringe products, from manual to high-speed, high-volume systems.
Key Responsibilities
As an Automation Process Engineer, your responsibilities will include:
* Developing and refining AVI machine recipes for pre-filled syringes to optimize performance.
* Supporting Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), and Performance Qualification (PQ) activities for AVI systems.
* Diagnosing and resolving vision system challenges, collaborating with vendors, subject matter experts, and the engineering team to minimize false rejects.
* Working closely with process experts and quality teams to ensure compliance with global standards and regulatory requirements.
Requirements
To be considered for this role, you should have:
* A degree in Engineering or a relevant scientific discipline.
* Experience working in a GMP-regulated pharmaceutical or biopharmaceutical environment.
* Hands-on expertise in Automated Visual Inspection systems and visual inspection standards.
Keywords
Automation Engineer | Process Engineer | AVI Systems | Pre-Filled Syringes | GMP | Vision Systems | FAT | SAT | Pharmaceutical Engineering | Quality & Compliance
Would you like any further refinements or additions?
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