Summary: Our client, a leading biopharmaceutical organisation based in Waterford, is seeking a Process Engineer to join them.
The successful candidate will play a key role in ensuring the reliable supply of syringe and vial products to patients globally.
The role involves supporting multiple platforms across inspection, assembly, labelling, and cartoning for autoinjectors, prefilled syringes, and vials, ranging from manual processes to high-speed, high-volume automated production lines.
Responsibilities: Provide process engineering support across manufacturing operations Support delivery of continuous improvement projects on existing equipment and processes Work closely with cross-functional teams, including technical, quality, and supply chain functions Apply knowledge of existing manufacturing technologies to support the development and implementation of new technologies, with a focus on improving output and yield Ensure compliance with safety and quality standards, providing technical support for process and equipment issues, and identifying and implementing process and product improvements Support qualification of new products and processes, including analysis of equipment performance data and management of improvement projects within budget and timelines Support new product introductions and capacity expansions, including vendor selection, maintenance planning, design changes, change control, and performance improvements Lead technical root cause investigations Support all safety and quality programmes and initiatives Qualifications & Experience: Degree in an Engineering discipline.
Experience in a highly regulated GMP environment.
Strong problem-solving and communication skills.
Strong documentation/protocol generation and execution skills.
Strong data analysis experience with equipment and integrated systems is desirable.