Swords Labs - Ireland Posted November 12, 2026

Senior Specialist, QA Technical Operations

Cruiserath, Ireland Full time
Quality Senior
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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.

Position Summary

BMS Cruiserath Biologics is seeking to recruit a Senior specialist, QA Technical Operations, Drug Substance. This is a 12 month fixed term contract role.

Reporting to the Senior Manager, QA Technical Operations, Drug Substance, the Senior specialist will support investigations within the Multi Product Cell Culture (MPCC) and supporting areas. The Senior specialist, QA Technical Operations will also be responsible for supporting qualification and validation activities, as well as New Product Introductions (NPI) and technical transfers. The role will support Engineering, Warehouse, Facilities, Utilities and Automation activities while also providing support for SAP, Maximo and Manufacturing Execution System (MES).

The role will be both challenging & rewarding and will ensure that the successful candidate can seize a wide range of development opportunities within BMS.

Key Responsibilities

Support review and approval of investigations within MPCC and supporting areas.

Facilitate the investigation triage business process and the daily investigations meeting.

Author, review, and approval of QA related procedures.

Support implementation of site initiatives to prevent deviation recurrence.

Promote Right First Time (RFT) approach within investigations process and drive accountability in meeting site investigation KPI’s.

Provide QA support for change controls, Projects, NPI and Tech Transfer Projects.

QA support for Maximo, Service Now, ALM and SAP related activities.

Provide QA support for site validation and qualification activities.

QA review and approval of Annual Product Quality Review reports (APQRs)

Review and approval of GMP documentation, including validation plans, protocols, reports, SOPs, forms, directives, policies and other validation documentation as required.

Drive and support a culture of continuous improvement initiatives and safe working practices.

Qualifications & Experience

The successful candidate must possess:

BSc in Science or a related discipline, with a minimum of 3 years Quality or related experience in the biopharmaceutical industry.

A clear understanding of cGMP requirements for areas of responsibility.

Demonstrated knowledge of deviation and change management processes.

Required to work on his/her own initiative in addition to working as part of a team. Must be capable of working across a team matrix to meet accelerated timelines.

Capable of positively influencing others to bring resolution to complex issues.

Excellent communication and presentation skills are essential.

Excellent time management and organizational skills along with a proven ability to multi-task.

Demonstrated ability to recognise issues, highlight risks and prioritise workload based on site goals and objectives.

Employees are expected to display the BMS values and behaviours, which enable them to be successful and perform at their highest level.

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-Hybrid

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/

For roles based in Washington State only: If you live in or expect to work from Washington State if hired for this position, please visit this page for important information about the Washington Fair Chance Act.

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.

R1608411 : Senior Specialist, QA Technical Operations

Job details

Seniority
Senior
Function
Quality
Therapeutic area
Not listed
Location
Cruiserath, Ireland
Employment type
Full time

How this role compares

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

We currently track 265 comparable Senior Quality roles across 63 biopharma companies.

265Comparable roles tracked
247Currently active
63Companies hiring similar roles
34Countries represented

Salary context

65 of 265 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Quality Control Chemist, Senior (Data Review) · Merck KGaA $25/hr – $39/hr (≈ $52,000–$81,120/yr)
Highest disclosed · Assoc Director, Quality Assurance · Gilead Sciences, Inc. $182,070/yr – $235,620/yr
Peer group range $66,560 – $208,845 (median $123,250)

Where these roles are based

Top locations among the 265 comparable roles

United States130
Ireland20
United Kingdom13
China10
Germany9
Switzerland9

+ 28 more countries

Seniority mix

265 of 265 peers have a known seniority level

Senior188
Associate Director43
Principal34

Therapeutic area mix

0 of 265 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

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.

60%similar
Mylan Teoranta Inverin, Ireland Senior
Same function Same seniority Same country
60%similar
Regeneron Ireland Limerick, Ireland Senior
Same function Same seniority Same country
60%similar
Regeneron Ireland Limerick, Ireland Senior
Same function Same seniority Same country
60%similar
AbbVie Sligo, ie Senior
Same function Same seniority Same country
60%similar
Abbott Clonmel, Tipperary, Ireland Senior
Same function Same seniority Same country
60%similar
BioMarin Pharmaceutical Inc. Cork, Ireland Senior
Same function Same seniority 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 Quality 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.

60%
Senior Microbiology Team Lead
Mylan Teoranta · Inverin, Ireland · Senior
Function Therapeutic area Seniority Country
60%
Senior QA Validation Specialist
Regeneron Ireland · Limerick, Ireland · Senior
Function Therapeutic area Seniority Country
60%
Senior Engineer, Global Process Validation
BioMarin Pharmaceutical Inc. · Cork, Ireland · Senior
Function Therapeutic area Seniority Country
60%
QC Microbiology Sr. Associate
Amgen Technology (Ireland) UC · Dublin, 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.