Swords Labs - Ireland Posted August 6, 2026

Specialist, Instrumentation Specialist (Standalone/Process Support Equipment)

Cruiserath, Ireland Full time
Manufacturing & CMC

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

Working with Us

Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .

Position summary:

BMS Cruiserath Biologics seeks to recruit permanent Senior Specialist Instrumentation who will be responsible for maintaining laboratory, standalone and process support equipment in the Manufacturing,  Laboratories and Warehouse/Cryogenics facilities.

The Senior Specialist, Instrumentation will report to the Manager, Standalone & Process Support Equipment Maintenance. A fundamental understanding of instrumentation and equipment qualification is desirable. Experience managing Vendors in a GMP environment extremely beneficial. Knowledge of Biopharmaceutical analytical platforms such as high and ultra performance liquid chromatography would be helpful, but not essential for the role.

Key responsibilities will include:

· Responsible for the calibration and maintenance program of laboratory/benchtop instruments, CTU’s, standalone assets and process support equipment in the following areas:

- MPCC (Multi-product Cell Culture) standalone test equipment/benchtop instruments and process support equipment.

- GMP and non-GMP Lab CTU’s (controlled temperature units)

- Non-GMP Upstream and Downstream Material Science and Technology Labs as well as Process Analytics lab equipment.

- Warehouse and Cryogenics standalone equipment.

· Working with Engineering Planners on scheduling and tracking of instrument maintenance and instrument lifecycle management.

· Management of Vendors working on site Including management of vendor RAMS (Risk Assessment/Method Statements).

· Review and approve documentation associated with analytical instrumentation qualification, calibration, and repairs.

· Responsible for work order management/compliance for all assets in scope.

· Participate, as part of a team, to deliver on the qualification of new instruments.

· Participate in and own internal Investigations and CAPA’s.

· Improvement and Optimization of Maximo PM’s/Job Plans and Data Sheets.

· Point of contact for projects and change controls associated with equipment in scope.

· Participate in troubleshooting of complex instrumentation/equipment issues.

· Leading Downtime (DT) and Failure Analysis exercises to ensure re-occurring failures are resolved,

with support from other functions.

· Ensuring compliance with all Safety and Environmental regulations, and compliance with corporate

policies, directives and current regulatory requirements for laboratory instrument qualification,

calibration and lifecycle management.

· Participate in internal and external regulatory audits, as required.

· Developing task specific Work Instructions (WI’s) and Risk Assessments (RA’s).

Requirements, Qualifications, Knowledge and Skills required include:

· The ideal candidate will hold a minimum of a Level 7 qualification in an engineering-related field or a BSc in a scientific discipline, complemented by at least three years of experience in a relevant role within a regulated manufacturing environment. Prior experience with instrument qualification in a GMP laboratory setting is highly desirable.

· A mechanical, electrical or calibration trade is desirable.

· Working knowledge of Maximo or equivalent CMMS system.

· High level of attention to detail and strong problem-solving abilities.

· Right First Time (RFT) and Reliability Excellence mindset.

· Excellent communication skills and the ability to work in a cross-functional collaborative environment.

#LI-Hybrid

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers

With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

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 for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

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 you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R1605055 : Specialist, Instrumentation Specialist (Standalone/Process Support Equipment)

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 1527 comparable Manufacturing & CMC roles across 125 biopharma companies.

1527Comparable roles tracked
1435Currently active
125Companies hiring similar roles
44Countries represented

Salary context

456 of 1527 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 · Senior Scientist II – CMC Developmental Sciences · AbbVie $0/hr – $0/hr (≈ $0–$0/yr)
Peer group range $0 – $540,400 (median $140,000)

Where these roles are based

Top locations among the 1527 comparable roles

United States782
India104
Germany74
Singapore67
France64
Ireland53

+ 38 more countries

Seniority mix

705 of 1527 peers have a known seniority level

Senior251
Manager165
Principal79
Associate68
Director64
Associate Director44
Senior Director21
Intern/Fellow/Postdoc8
Executive/VP5

Therapeutic area mix

7 of 1527 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease6
Oncology1

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
Lilly Cork, Cork, Ireland Manager
Same function Same country
40%similar
McDermott Laboratories Limited Northern Cross, Ireland Director
Same function Same country
40%similar
Gilead Sciences Ireland UC Dublin, Ireland Manager
Same function Same country
40%similar
Gilead Sciences Ireland UC Cork, Ireland Associate 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

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%
Sr. Associate/Manager - Global CMC Regulatory Associate
Lilly · Cork, Cork, Ireland · Manager
Function Therapeutic area Seniority Country
40%
Associate Director, Commercial Supply Chain Governance & Reporting
Gilead Sciences Ireland UC · Cork, Ireland · Associate Director
Function Therapeutic area Seniority Country
40%
Technical Services Lead (3 Year FTC)
Mylan Teoranta · Inverin, Ireland · Seniority not listed
Function Therapeutic area Seniority Country
40%
Senior Process Engineer
Mylan Teoranta · Inverin, 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.