Director, QC Automation

Bristol-Myers Squibb; Harvard (MA); On-site; USD 184,000 - 239,000; Full time

Job summary

Bristol Myers Squibb is seeking a Director of QC Automation to own the deployment and lifecycle of Automated QC capabilities across the Cell Therapy manufacturing network. You will coordinate priorities with ADA, AS&T, and receiving sites to ensure reliable deployment and cGMP compliance.

Responsibilities include defining system requirements, leading cross-site deployments, and driving risk mitigation. This role requires 12+ years in regulated pharma, 5+ years in automation deployment, and up to

Qualifications

• 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.

Responsibilities

• 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.

Skills

cGMP knowledge

Automated lab tech

Cross-functional leadership

Stakeholder management

Problem solving

Job description

Working with UsChallenging. 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 .Position SummaryThe 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.Key ResponsibilitiesOwn 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.QualificationsKnowledge, Skills & AbilitiesIn 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.Education & Experience12+ 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.Compensation Overview:Devens - MA - US: $197,470 - $239,290Madison - Giralda - NJ - US: $184,550 - $223,634Princeton - NJ - US: $184,550 - $223,634 Seattle - WA: $203,010 - $245,995The 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 on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:Health Coverage: Medical, pharmacy, dental, and vision care.Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.Work-life benefits include:Paid Time OffUS Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidaysBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.*Eligibility Disclosure: T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.Uniquely Interesting Work, Life-changing CareersWith a single vision as inspiring as “Transforming patients’ lives through science ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.Supporting People with DisabilitiesBMS 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 [e-mail] . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.Candidate RightsBMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.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/Data ProtectionWe 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 you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at [e-mail] . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.R1605230 : Director, QC Automation