Specialist, Reliability Technician – GMP Maintenance (Days)

Bristol Myers Squibb UK & Ireland; Leinster; On-site; EUR 42,000 - 56,000; Full time

Benefits offered by this job

Annual bonus

Pension contribution

Family medical allowance

27 days annual leave

Life assurance

On-site gym

Job summary

Bristol Myers Squibb UK & Ireland is seeking a permanent Specialist, Reliability Technician – GMP Maintenance (Days) for our Cruiserath site in Ireland. The role focuses on safe, compliant maintenance of GMP manufacturing equipment, supporting calibration, troubleshooting and continuous improvement.

You will work with Manufacturing, Quality, and Engineering to deliver planned and unplanned maintenance, manage CMMS records, and contribute to reliable, high-quality operations in a fast-paced

Qualifications

• Minimum Level 6 qualification in Electrical, Instrumentation, Mechanical or related technical discipline.
• 2–4 years' experience in a maintenance/engineering role within a regulated manufacturing environment.
• Experience using a CMMS such as Maximo.
• Strong troubleshooting and adherence to procedural compliance and documentation.

Responsibilities

• Execute preventative, predictive, corrective and condition-based maintenance activities.
• Troubleshoot and diagnose faults across mechanical, electrical, instrumentation, automation and utility systems.
• Respond to equipment failures and support safe return to service.
• Perform or support calibration and other maintenance interventions as required.
• Support planned shutdowns, outages and major maintenance activities.

Skills

Safety mindset

Troubleshooting

Attention to detail

Communication

Teamwork

Ownership

Flexibility

Education

Level 6 qualification (Electrical/Instrumentation/Mechanical)

Tools

Maximo CMMS

Job description

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose‑driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

The Role

BMS Cruiserath Biologics is seeking to recruit a permanent Specialist, Reliability Technician – GMP Maintenance (Days).

Position Summary

The Reliability Technician is a permanent, hands‑on technical role within the GMP Maintenance Days Team, responsible for the safe, compliant and effective maintenance of GMP manufacturing equipment and associated systems.

The role executes planned and unplanned maintenance activities, including preventative and predictive maintenance, calibration support and equipment troubleshooting. A key focus is maintaining equipment reliability, ensuring high‑quality maintenance execution and supporting the continued safe and compliant operation of the manufacturing facility.

The Reliability Technician works collaboratively with Manufacturing, Quality, Engineering, Reliability Engineering, Maintenance Planning and specialist vendors to resolve equipment issues, improve maintenance strategies and support continuous improvement initiatives.

Key Responsibilities

Maintenance & Troubleshooting

• Execute preventative, predictive, corrective and condition‑based maintenance activities.
• Troubleshoot and diagnose equipment faults across mechanical, electrical, instrumentation, automation and utility systems within individual competency levels.
• Respond to equipment failures and support the safe and timely return of equipment to service.
• Perform or support calibration and other maintenance interventions as required.
• Support planned shutdowns, outages, major maintenance activities and equipment overhauls.

Safety, Quality & GMP Compliance

• Perform all maintenance activities in accordance with applicable EHS, GMP and site requirements.
• Follow relevant safe systems of work, including LOTO and permit‑to‑work requirements.
• Complete maintenance activities and documentation in accordance with approved procedures and Good Documentation Practices.
• Maintain high standards of housekeeping, training compliance and audit readiness.
• Support audits, inspections, deviation investigations, CAPAs and change controls where required.

Reliability & Work Management

• Complete assigned work orders safely, compliantly and to the required quality and schedule.
• Record maintenance interventions, failure information and asset history accurately within the CMMS.
• Identify and elevate recurring equipment issues and emerging reliability risks.
• Support root cause investigations and implementation of appropriate corrective and preventative actions.
• Provide practical input into maintenance strategies, job plans, PM optimisation and spare‑parts strategies.
• Work closely with Maintenance Planning, Reliability Engineering and Manufacturing to coordinate and prioritise maintenance activities.

Continuous Improvement & Teamwork

• Identify opportunities to improve equipment reliability, maintenance effectiveness and ways of working.
• Participate in Operational Excellence and cross‑functional improvement initiatives.
• Contribute to the development and improvement of SOPs, maintenance procedures and job plans.
• Support the introduction and effective use of maintenance tools, technologies and best practices.
• Provide clear written and verbal handovers when required.
• Share technical knowledge and support the training and development of colleagues.
• Collaborate effectively with Manufacturing, Quality, Engineering and external service providers.

Required Qualifications & Experience

• Minimum Level 6 qualification in Electrical, Instrumentation, Mechanical or a relevant related technical/engineering discipline, or equivalent technical competence demonstrated through substantial relevant maintenance/engineering experience in a regulated manufacturing environment.
• 2–4 years' experience in a maintenance or relevant engineering role within a regulated manufacturing environment.
• Strong troubleshooting and problem‑solving capability.
• Ability to work safely and effectively both independently and as part of a cross‑functional team.
• Strong attention to detail and commitment to procedural compliance and high‑quality maintenance documentation.

Desirable

• Trade qualification or additional relevant technical certification.
• Experience within biopharmaceutical, pharmaceutical, medical device or another regulated manufacturing environment.
• Experience using a CMMS such as Maximo.
• Experience with preventative or predictive maintenance, calibration or condition‑based maintenance techniques.
• Experience supporting equipment investigations, root cause analysis or reliability improvement activities.

What We're Looking For

The successful candidate will demonstrate

• A strong Safety and Quality First mindset.
• Strong practical troubleshooting and problem‑solving skills.
• Attention to detail and procedural compliance.
• Effective communication and teamwork.
• Personal accountability and ownership.
• Flexibility and willingness to learn and develop.
• The ability to prioritise work and manage competing demands within a dynamic manufacturing environment.

Working Arrangements

• Day‑based role supporting GMP manufacturing operations.
• Work may include manufacturing, cleanroom, laboratory, utility plant and external utility areas.
• Participation in planned shutdowns, outages and project activities may be required based on business needs.

Why you should apply

• You will help patients in their fight against serious diseases.
• You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees.
• You’ll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical allowance, 27 days of annual leave, life assurance and on‑site gym.

How We Work

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models site‑essential, site‑by‑design, field‑based and remote‑by‑design. The model assigned to this role is based on its core responsibilities. Learn more at https //careers.bms.com/ways-of-working.

Supporting People With Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [e-mail]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information https //careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https //careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If this posting is missing required information required by local law or incorrect, contact BMS at [e-mail] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1607254 Specialist, Reliability Technician – GMP Maintenance (Days)