Director, QC Automation

Bristol Myers Squibb

Bristol Myers Squibb Director deploying automated quality-control systems across Cell Therapy manufacturing. Owning AQC technology lifecycle, network rollout, compliance, and team leadership.

Posted 8/14/2026full-timeSeattle • Massachusetts, New Jersey, Washington • 🇺🇸 United StatesLead💰 $184,550 - $245,995 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing the technology roadmap for Automated QC systems, ensuring compliance with cGMP requirements, and leading cross-functional teams in a regulated pharmaceutical environment. Proven ability to drive deployment strategies, mitigate risks, and establish performance metrics.

Highest-signal resume keywords

CGMP KnowledgeAutomated Laboratory TechnologiesCross-Functional Team LeadershipStakeholder ManagementTechnology Deployment Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Automated QC Systems ManagementRegulatory ComplianceRisk MitigationPerformance Metrics EstablishmentTechnology Transfer Projects

Soft Skills

Problem-SolvingInfluencing SkillsCoaching and Development

Industry Keywords

Pharmaceutical RegulationsBiotech ManufacturingQuality ReadinessOperational ReadinessDeployment Timeline Management

About the role

Key responsibilities & impact

Own the technology roadmap and lifecycle for Automated QC equipment and software, including upgrades, vendor management, and long-term platform planning
Lead deployment of Automated QC systems at new and existing nodes across the Cell Therapy manufacturing network
Sequence and coordinate priorities across concurrent programs
Partner with Assay and Data Automation and Analytical Sciences and Technology to define system requirements, validate performance, and resolve technical issues
Serve as primary point of contact for receiving sites and ensure operational and quality readiness before go-live
Represent Automated QC strategy and progress in network-level technical and governance forums
Identify deployment timeline and system performance risks and drive mitigation plans
Ensure Automated QC systems and processes meet cGMP requirements
Support regulatory filings as needed
Establish key performance metrics and report deployment progress to stakeholders and leadership
Lead, coach, and develop the team supporting deployment and sustaining operations

Requirements

What you’ll need

In-depth knowledge of cGMPs and pharmaceutical regulations
Experience with automated laboratory or analytical technologies
Proven ability to lead cross-functional teams and coordinate competing priorities across multiple programs
Strong stakeholder management and influencing skills within a matrix organization
Solid problem-solving and risk-mitigation skills
12+ years of relevant experience, preferably in a regulated pharmaceutical or biotech manufacturing environment
5+ years leading technology deployment, automation, or tech transfer projects
Occasional travel required, up to 25%

Benefits

Comp & perks

Competitive benefits, services and programs
Medical, pharmacy, dental, and vision care
BMS Well-Being Account
BMS Living Life Better
Employee Assistance Programs (EAP)
401(k) plan
Short- and long-term disability insurance
Life insurance
Accident insurance
Supplemental health insurance
Business travel protection
Personal liability protection
Identity theft benefit
Legal support
Survivor support
Flexible time off (unlimited, with manager approval) for US exempt employees
11 paid national holidays for US exempt employees
160 hours annual paid vacation for eligible new hires
3 optional holidays for eligible employees
Unlimited paid sick time, based on eligibility
Up to 2 paid volunteer days per year
Summer hours flexibility, based on eligibility
Leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs
Annual Global Shutdown between Christmas and New Years Day
Reasonable workplace accommodations/adjustments and ongoing support
Additional incentive cash and stock opportunities, based on eligibility