Director, QC Automation

Bristol Myers Squibb

. Own the technology roadmap and lifecycle for Automated QC equipment and software, including upgrades, vendor management, and long-term platform planning .

Posted 9/22/2026full-timeUnited StatesLead💰 $184,550 - $245,995 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in leading technology deployment and automation projects within regulated pharmaceutical environments, ensuring compliance with cGMP requirements and effective stakeholder management. Proven ability to coordinate cross-functional teams and drive performance metrics for successful project execution.

Highest-signal resume keywords

Technology Deployment LeadershipCGMP Compliance KnowledgeAutomated Lab Technologies ExperienceCross-Functional Team CoordinationStakeholder Management Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Technology Roadmap ManagementAutomated QC Systems DeploymentRisk Mitigation PlanningPerformance Metrics EstablishmentRegulatory Filing Support

Soft Skills

Problem-Solving SkillsInfluencing SkillsCoaching and Development Skills

Industry Keywords

Pharmaceutical ManufacturingBiotech ManufacturingRegulated EnvironmentAssay and Data AutomationAnalytical Sciences

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 or system-performance risks and drive mitigation plans
Ensure 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

12+ years of relevant experience, preferably in a regulated pharmaceutical or biotech manufacturing environment
5+ years leading technology deployment, automation, or tech transfer projects
In-depth knowledge of cGMPs and pharmaceutical regulations
Experience with automated lab 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
Occasional travel required, up to 25%
Willingness to work at one of the listed U.S. locations: Devens, Massachusetts; Madison, New Jersey; Seattle, Washington; or Princeton, New Jersey

Benefits

Comp & perks

Additional discretionary incentive cash and stock opportunities
Wellbeing support
Retirement and financial protection benefits
Medical, dental, vision, life and disability insurance offerings
Flexible Time Off (FTO) without a set accrual limit for U.S.-based exempt employees
11 paid company holidays each year
160 hours of paid vacation annually for eligible new hires
3 optional holidays for eligible non-exempt, RayzeBio, and Puerto Rico employees
Paid sick leave, depending on eligibility
Up to two paid volunteer days per year
Summer hours flexibility
Medical, personal, parental, caregiver, bereavement, and military leaves of absence
Annual Global Shutdown between Christmas Day and New Year's Day for eligible employees
Workplace accommodations/adjustments and ongoing support for people with disabilities