Maintenance Technician

biomarin; Cork; On-site; EUR 40,000 - 55,000; Full time

Job summary

BioMarin is seeking a Maintenance Technician for their facility in Cork to maintain and optimize equipment for GMP compliance. The role involves executing maintenance activities plant-wide, troubleshooting equipment failures, and interacting with process partners for continuous improvement.

The ideal candidate will have a relevant engineering qualification and at least 3 years of experience in a GMP environment, particularly within the bio-pharmaceutical sector. A strong focus on safety and compliance is essential.

Qualifications

• Proven experience in equipment maintenance and troubleshooting in GMP environments.
• Experience in the bio-pharmaceutical industry preferred.

Responsibilities

• Proactively maintain process, utility, and facility equipment.
• Perform maintenance and troubleshooting of equipment.
• Ensure compliance with all procedures and regulations.

Skills

cGMP regulations

equipment maintenance

troubleshooting

safety awareness

problem-solving

Education

Relevant third level qualification in Engineering

3+ years’ experience in a GMP environment

Job description

Maintenance Technician - Shanbally, Ringaskiddy, Cork

Duration: One-year contract position with possible extension based on performance

Schedule: Mon- Wed - 3 Day

Thurs- Friday - Off

Mon- Tue- 2 Night

Wed+ Fri+ Weekend- Off

BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting‑edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.

A high level of initiative, energy and motivation are key role requirements, as well as excellent organizational skills.

The Maintenance Technician reports to the Manager, Maintenance Operations, and is responsible for executing maintenance and utility activities plant wide in a GMP‑compliant manner. The Maintenance Technician maintains equipment in the following areas: manufacturing operations including Upstream & Downstream processing, Material Storage & Dispensing, Packaging, Drug Product Fill Finish, Clean & Plant Utility systems, WWTP and HVAC, reliability programs and capital engineering projects. The Maintenance Technician will serve as an integral member of Maintenance Operations team in a Biologics drug substance and product manufacturing facility.

Responsibilities:

• Proactively maintain process, utility and facility equipment in accordance with cGMP regulations, applicable safety considerations, Standard Operating Procedures, best maintenance practices and the reliability agenda.
• Maintenance and troubleshooting of equipment.
• Interact with all process partners to continuously improve operations by recognising and correcting the causes of less than optimal equipment, facility and team performance.
• Manage external vendor support to complete required services in a GMP compliant manner.
• Perform problem solving including root cause analysis as required when equipment failures result in loss of production, substandard equipment performance and substantial repair cost and/or personnel safety incidents.
• Ensure Electrical, Process and Utility Systems are maintained in a controlled state thus ensuring compliance with all procedures and regulations and reliability initiatives.
• Maintain a safe working environment by continuously promoting safety awareness, recognising and rectifying unsafe conditions and performing thorough investigations when accidents occur.
• Record all maintenance work performed on the site CMMS system.
• Respond to critical utility alarms generated from the site automated alarm messenger system.
• Maintain documentation and management and control systems in compliance with cGMP regulations and training instructions.
• Where required complete and record calibrations activities completed on site and report any defects detected.
• Contribute to the drive to effectively manage spares, consumables and contracts in a timely and cost effective manner.
• Use of permit to work system or other safety systems to control engineering activities.
• Participation in HAZOP and design reviews

Scope:

• This position ensures the Manufacturing, Quality Control, and Facilities equipment and instrumentation is maintained & operated in the calibrated state necessary to perform cGMP activities.
• Maintenance Technician has scope to initiate process, cost and execute continuous improvement ideas.

Education and Experience:

A relevant third level qualification in Engineering or time-served apprenticeship with 3+ years’ experience in a GMP environment, preferably Bio‑pharmaceuticals or equivalent industry with drug product fill finishing and packaging activities.

Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.

Equal Opportunity Employer/Veterans/Disabled

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.