About the Opportunity
We are currently recruiting for an exciting opportunity with a leading pharmaceutical organization based in Mayo.
This is an excellent position for anyone looking to join a multinational company that excels in its field. This is a 12-month fixed-term contract, and the successful candidate will report directly to the Associate Director, Maintenance.
Job Summary
The ideal candidate will have at least two years of process/equipment engineering experience in an Aseptic/Cleanroom environment. They will be responsible for providing engineering support to the manufacturing team, troubleshooting equipment issues, and identifying process improvement opportunities.
Key Responsibilities
* Provide engineering support and technical troubleshooting to all site operations, ensuring the reliability of equipment and processes by implementing continuous improvement initiatives.
* Support the business unit (BU) in developing robust processes and systems to ensure effective quality delivery.
* Maintain line processes, equipment, and materials to achieve consistent, reliable, and predictable process performance and product quality.
* Develop and implement systems and structures to minimize technical downtime on the line.
* Resolve technical issues effectively and efficiently with the technical team to support operations.
* Drive continuous improvement and process efficiency programs, such as OEE, OPEX, RCA, RCM, and productivity output for the BU.
* Assist with trending, monitoring, and performance of equipment to reduce unplanned downtime.
* Help manage, track, and monitor relevant KPIs for the Technical Team.
* Assist with trending, monitoring, and reduction of repeat deviations associated with equipment and technology in the BU.
* Generate and approve associated change controls and protocols.
* Support the BU during regulatory and compliance audits.
Requirements
* Bachelor's degree in a relevant Engineering area.
* At least two years of experience in process engineering, including batch processing, automation, project management, commissioning, and validation, as well as equipment reliability and continuous improvement.
* Knowledge of cGMP and regulatory requirements relating to the Healthcare industry.
* Demonstrated project management skills, including the ability to deliver projects on schedule, within budget, and meeting predefined quality requirements.
Salary: €65,000 - €85,000 per annum