Swords Labs - Ireland Posted October 7, 2026

Specialist, Reliability Technician – GMP Maintenance (Days)

Cruiserath, Ireland Full time
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Swords Labs - Ireland is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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 escalate 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.

Qualifications & Experience

Required

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

#LI-Onsite

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

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  adastaffingsupport@bms.com . 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  TAEnablement@bms.com 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)

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Cruiserath, Ireland
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 3753 comparable Manufacturing & CMC roles across 173 biopharma companies.

3753Comparable roles tracked
3372Currently active
173Companies hiring similar roles
64Countries represented

Salary context

921 of 3753 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Biologics Support Operator I (3rd Shift) · AbbVie $14/hr – $26/hr (≈ $29,099–$54,122/yr)
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $41,610 – $381,150 (median $125,550)

Where these roles are based

Top locations among the 3753 comparable roles

United States1739
Germany251
India166
France146
Ireland136
China123

+ 58 more countries

Seniority mix

1670 of 3753 peers have a known seniority level

Senior431
Manager381
Intern/Fellow/Postdoc259
Associate162
Principal138
Associate Director119
Director115
Senior Director57
Executive/VP8

Therapeutic area mix

24 of 3753 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease15
Rare Disease3
Oncology3
Respiratory1
Dermatology & Aesthetics1
Immunology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
McDermott Laboratories Limited Northern Cross, Ireland Director
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland Senior
Same function Same country
40%similar
McDermott Laboratories Limited Northern Cross, Ireland
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland Director
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Manufacturing & CMC job in Ireland, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Director, Combination Product Development
McDermott Laboratories Limited · Northern Cross, Ireland · Director
Function Therapeutic area Seniority Country
40%
Senior Process Engineer
Mylan Teoranta · Inverin, Ireland · Senior
Function Therapeutic area Seniority Country
40%
Associate Biotech Production Specialist
Regeneron Ireland · Limerick, Ireland · Associate
Function Therapeutic area Seniority Country
40%
Sr. Automation Engineer - Packaging
Amgen Technology (Ireland) UC · Dun Laoghaire, Ireland · Senior
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.