Director, QC Automation

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 .

Summary The Director, QC Automation owns the deployment and lifecycle of Automated QC (AQC) capabilities across the Cell Therapy manufacturing network. Acting as the technology owner for AQC equipment and software, this role coordinates priorities across multiple programs and partners closely with Assay and Data Automation (ADA), Analytical Sciences and Technology (AS&T), and receiving sites to ensure AQC systems are deployed reliably, on schedule, and in a state of control.

Own the technology roadmap and lifecycle for AQC equipment and software, including upgrades, vendor management, and long-term platform planning. Lead deployment of AQC systems at new and existing nodes across the network, sequencing and coordinating priorities across concurrent programs. Partner with ADA and AS&T to define system requirements, validate performance, and resolve technical issues. Serve as the primary point of contact for receiving sites, ensuring operational and quality readiness ahead of go-live. Represent AQC strategy and progress in network-level technical and governance forums. Identify risks to deployment timelines or system performance and drive mitigation plans. Ensure AQC 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 AQC deployment and sustaining operations.

Knowledge, Skills & Abilities 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.

12+ years of relevant experience, preferably in a regulated pharmaceutical or biotech manufacturing environment. 5+ years leading technology deployment, automation, or tech transfer projects. Travel: occasional travel required (up to 25%). 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.

Overview: Devens - MA - US: $197,470 - $239,290
Madison - Giralda - NJ - US: $184,550 - $223,634
Princeton - NJ - US: $184,550 - $223,634 
Seattle - WA: $203,010 - $245,995
 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.  Eligibility for specific benefits listed