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Biologics Maintenance Engineer, Westmeath
Client: TEAM HORIZON
Location: Westmeath, Ireland
Job Category: Other
EU work permit required: Yes
Job Reference: 118f4fb02359
Job Views: 4
Posted: 03.06.2025
Expiry Date: 18.07.2025
Job Description:
Team Horizon is seeking a Biologics Maintenance Engineer for a leading pharmaceutical company based in Athlone.
The Biologics Maintenance Engineer is responsible for managing routine and non-routine maintenance activities carried out by maintenance technicians, including all upstream and downstream production equipment and systems. This role involves planning, coordination, and scheduling of maintenance works performed by service vendors in a DS environment. The individual will represent the company's interests, objectives, and policies professionally and responsibly, reporting to the Biologics Engineering Manager, with opportunities for personal and career development.
Why you should apply:
* Our client has a culture of innovation, inclusion, and development, and is recognized as a great place to work.
* This is an excellent opportunity to join a world-class manufacturing operation delivering high-quality medicines globally.
* Excellent contracting rates are on offer.
What you will be doing:
* Ensuring all EHS responsibilities are met according to regulations and procedures, including Risk Assessments, RAMS, and GEMBAs.
* Supporting new equipment installations and product introductions.
* Maintaining the Maintenance Quality System in compliance with SOPs, policies, and cGMP requirements.
* Planning and coordinating scheduled and unscheduled maintenance tasks.
* Managing spare parts, change parts, and equipment within the DS facility and Engineering Stores.
* Maintaining the Maintenance Management System accurately.
* Utilizing and maintaining IT systems like Calibration and Maintenance Management Systems.
* Leading shift handovers and reporting issues via Tier meetings.
* Providing support to Operations, Validation, Engineering, and Quality teams as needed.
What you need to apply:
* An Associate Degree and/or certification in a mechanical, electrical, or related field.
* 3-5 years of experience in a cGMP commercial manufacturing environment, preferably with upstream (cell culture) and downstream purification experience.
* Hands-on experience with CMMS and Calibration Systems.
* Experience with Quality Management Systems, strong interpersonal, communication, and technical problem-solving skills.
* Knowledge of cGMP for process equipment, instrumentation, and calibration; knowledge of Six Sigma and lean systems is an advantage.
* Ability to make informed, timely decisions considering facts, goals, constraints, and risks.
* A proactive team player with a passion for improvement.
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