JuN - Seattle Dexter Posted November 4, 2026

Director, ASAT Systems and Technology Sciences

Devens, United States Full time
Notify me about similar jobs

JuN - Seattle Dexter 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

The Director of ASAT Systems and Technology Sciences provides strategic and technical leadership for Cell Therapy laboratory systems, digital technologies, and data platforms across the Cell Therapy global manufacturing network. This role is accountable for the long-term technology strategy, governance, innovation, and lifecycle management of GMP laboratory systems, driving network-wide digital transformation, operational excellence, compliance, and continuous improvement. As a recognized technical leader, the Director influences cross-functional strategy, leads highly complex and high-impact initiatives, and translates emerging technologies and industry trends into business value and organizational capability

Duties/Responsibilities

Define and execute the long-term strategy, governance model, and roadmap for laboratory systems, digital technologies, data platforms, and analytical capabilities supporting Cell Therapy laboratory operations.

Establish strategic priorities that align technology investments with business objectives, regulatory requirements, and operational needs.

Serve as the technology and business leader for laboratory systems and digital capabilities across the Cell Therapy laboratory network.

Drive network-level decisions regarding laboratory digitalization, automation, data management, and systems integration.

Provide oversight for lifecycle management, governance, enhancement, and expansion of GMP laboratory systems and technology platforms.

Ensure alignment, standardization, and harmonization of laboratory systems, processes, data standards, and business practices across sites and functions.

Partner with Quality, Manufacturing, Technical Operations, IT, Digital, Regulatory, and Supply Chain organizations to establish future-state capabilities and technology solutions.

Ensure laboratory systems remain inspection-ready, compliant, secure, and aligned with global regulatory expectations and data integrity requirements.

Sponsor strategic initiatives related to system modernization, automation, integration, analytics, and digital transformation.

Lead highly visible, complex, and high-impact initiatives that improve laboratory performance, compliance, efficiency, and business outcomes.

Drive innovation by identifying and implementing new technologies, advanced analytics, automation tools, and digital solutions.

Challenge existing processes and practices to deliver sustainable improvements and organizational transformation.

Establish metrics and governance processes to monitor system performance, user adoption, operational effectiveness, and business value realization.

Translate industry best practices and emerging technologies into strategic initiatives that strengthen Cell Therapy capabilities.

Lead cross-functional teams supporting large, complex, high-risk, or high-value initiatives across multiple sites and technology platforms.

Represent ASAT and Quality organizations in strategic governance forums, leadership reviews, inspections, and regulatory interactions.

Foster a culture of accountability, innovation, scientific excellence, inclusion, and continuous learning.

Serve as a mentor and role model, influencing culture, leadership behaviors, and technical excellence across teams and functions.

Reporting Relationship

This position will report to the Executive Director of Analytical Sciences and Technology (ASAT), Cell Therapy.

Qualifications

Bachelor's degree in a scientific, engineering, information systems, or related discipline required; advanced degree (MS or PhD) preferred.

12+ years of relevant experience (or equivalent combination of education and experience) within biotechnology, pharmaceuticals, cell therapy, gene therapy, or biologics manufacturing environments.

6+ years of leadership experience managing technical teams and complex cross-functional programs.

Demonstrated experience leading network-scale laboratory systems, digital transformation, automation, informatics, quality systems, or technology-enabled business initiatives.

Proven success developing and executing strategic roadmaps that drive operational excellence, compliance, scalability, and business value.

Demonstrated ability to influence senior leadership and successfully lead large, complex, high-risk, or high-visibility programs across multiple sites, functions, and technology platforms.

Extensive knowledge of GMP regulations, data integrity principles, quality systems, risk management, and commercial manufacturing operations.

Strong enterprise mindset and business acumen with the ability to make decisions that balance operational needs, regulatory requirements, and long-term business objectives.

Exceptional leadership, influencing, and stakeholder management skills with demonstrated success driving alignment across Quality, Manufacturing, Technical Operations, IT, and other cross-functional organizations.

Demonstrated ability to identify emerging technologies, industry trends, and innovative solutions and translate them into business value and organizational capability.

Proven ability to build, develop, and lead high-performing teams through coaching, mentoring, succession planning, and organizational development.

Excellent communication and executive presence with the ability to effectively engage in senior leadership, regulatory agencies, external partners, and industry forums.

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.

Compensation Overview:

Devens - MA - US: $201,430 - $244,089
Seattle - WA: $207,080 - $250,929
Summit West - NJ - US: $188,250 - $228,114


The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.

Benefits:

Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans – including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability).

U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year.

Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.

Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day.

U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits

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.

R1606392 : Director, ASAT Systems and Technology Sciences

Job details

Seniority
Director
Function
Quality
Therapeutic area
Not listed
Location
Devens, United States
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 103 comparable Director Quality roles across 30 biopharma companies.

103Comparable roles tracked
99Currently active
30Companies hiring similar roles
21Countries represented

Salary context

53 of 103 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 · Senior Principal Microbiologist · Lilly $65,250/yr – $169,400/yr
Peer group range $117,325 – $320,000 (median $219,375)

Where these roles are based

Top locations among the 103 comparable roles

United States77
Netherlands3
Japan3
Germany2
Ireland2
Singapore1

+ 15 more countries

Seniority mix

103 of 103 peers have a known seniority level

Director45
Principal33
Senior Director25

Therapeutic area mix

0 of 103 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
AbbVie North Chicago, IL Director
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Warren, United States Director
Same function Same seniority Same country
60%similar
Celgene - Summit (Corp) Summit West, United States Director
Same function Same seniority Same country
60%similar
Sarepta Therapeutics, Inc. Bedford, United States Director
Same function Same seniority Same country
60%similar
Kite Pharma, Inc. Santa Monica, United States Director
Same function Same seniority Same country
60%similar
Teva Pharmaceuticals Davie, Florida, United States Director
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 the United States, 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%
Director, Clinical Quality Assurance
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
60%
Director, Corporate Quality - GCP
Sarepta Therapeutics, Inc. · Bedford, United States · Director
Function Therapeutic area Seniority Country
60%
Director Quality Function
Teva Pharmaceuticals · Davie, Florida, United States · Director
Function Therapeutic area Seniority Country
60%
Director, Digital Quality GMP Computer Oversight
Gilead Sciences, Inc. · Frederick, United States · Director
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.