Senior Manager, Principal Engineer, MSAT in Summit, NJ

Company: Bristol-Myers Squibb
Location: Summit
Posted on: May 24, 2025

Job Description:

Senior Manager, Principal Engineer, MSAT in Summit, NJ page is loadedSenior Manager, Principal Engineer, MSAT in Summit, NJApply locations Summit West - NJ - US time type Full time posted on Posted 11 Days Ago job requisition id R1589814Working 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 .At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there's no better place than here at BMS with our Cell Therapy team.This Senior Manager, Principal Engineer, MSAT Process Engineering is responsible for supporting the production of personalized cell therapy products for both global clinical trials and commercial supply for multiple products.Areas of responsibility include (a) providing day-to-day manufacturing support, (b) leading manufacturing investigations pertaining to the process control strategy and associated elements, (c) managing multidisciplinary projects aimed at improving the process and/or drug product life cycle sustainability, (d) managing CPV and process monitoring program, and (e) support development and lifecycle management of MBR, MES, and/or eBR.These areas include creation/revision of documentation (i.e. SOP, change control, validation documentation, technical reports, etc.) and management of internal / external team of resources (e.g. engineers and/or scientists) required to support the production of personalized cell therapy products. Cross-functional collaboration with SMEs from the Development Group, Manufacturing Group, Supply Chain Group, and Quality Group is essential to ensuring technical support is delivered to a rapidly growing CAR-T manufacturing organization.Shifts Available:Monday - Friday, Standard Working Hours, OnsiteResponsibilities:

• Managing up to 6 direct reports.
• Support all MS&T activities to ensure uninterrupted clinical/commercial supply.
• Knowledge of cGMPs and multi-national biopharmaceutical regulations. Cell therapy experience is a major plus.
• Ensure Safe and Compliant cGMP operations through technical process support for routine clinical/commercial batches and assist QA with on time closure of all quality system records such as deviations, CAPAs and change controls.
• Knowledge of the relationship between manufacturing processes, ERP, and MES a major plus
• Must have excellent organization skills and ability to handle multiple tasks.
• Hands-on experience with single-use technologies, closed systems, and cold chain/cryogenic technologies.
• Lead team of engineering and/or scientists for front-line support of the manufacturing process for cell therapies.
• Support product quality evaluations and investigations ensuring compliance with internal standards and regulatory requirements.
• Possess strong verbal/written communication skills.
• Ability to think strategically and to translate strategy into actions.
• Support Continued Process Validation (CPV) and lead team in support of Statistical Process Control monitoring program and Statistical Alert Event evaluations/investigations.
• Develop, understand, and manage tools/templates to monitor manufacturing process performance and enable understanding of process capability.
• Collaborate within the plant and across the Network
• Promote mindset of continuous improvement, problem solving, and prevention.Knowledge and Skills:
  • Exhibit exceptional team leadership skills.
  • Demonstrated experience and implementation success with various Agile methodologies.
  • Excellent oral and written communication and presentation skills. Ability to influence at all levels.
  • Advanced critical reasoning and decision-making skills.
  • Ability to think strategically and translate strategy into actions.
  • Ability to work independently and in cross-functional teams.
  • Advanced technical document writing.
  • Advanced time management skills, including prioritizing and managing expectations in a fast-paced working environment.
  • Must have excellent organization skills and ability to manage multiple tasks.
  • Operate effectively and with moderate supervision within a team or independently, performing projects and related duties.
  • Intermediate knowledge of MS Office Applications.
  • Working knowledge of Electronic Batch Records (EBR), Review by Exception (RBE), and MES Recipe object lifecycle management preferred.
  • Experience with HP ALM, Electronic Document Management Systems, and Change Management Systems preferred.
  • Knowledge of cGMPs and multi-national biopharmaceutical regulations. Cell therapy experience is preferred.
  • Knowledge of the relationship between manufacturing processes, ERP, and MES preferred.
  • Experience with single-use technologies, closed systems, and cold chain/cryogenic technologies is preferred.
  • Proficiency utilizing MS Office products and working knowledge of statistical software (R, JMP, Minitab) required.
  • Possess strong verbal and written communication skills.
  • Ability to communicate honestly, transparently, and effectively with peers, department management, and cross-functionally.
  • Hands-on experience preferred with CAR T or biopharmaceutical manufacturing and Quality Control
  • Proven delivery of complex investigation reports preferred.
  • Ability to coach, develop, delegate, and motivate others.
  • Ability to develop, delegate, and motivate others.Basic Requirements:
    • Biochemical, Chemical, Biomedical Engineering or Cell Biology/Immunology discipline with
      • B.S. with 8-10 years of relevant experience
      • M.S with 7-10 years of relevant experience
      • Ph.D. with 5-7 years of relevant experience
      • Experience level will determine position title and enterprise grade level.
      • Four 4+ years of leadership, technical transfer, strategy lead, and management experience.
      • Understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique, packaging, shop floor quality, batch review, or disposition preferred
      • Experience with MES, ERP, LIMS, or other manufacturing boundary systems
      • Flexibility to work within manufacturing schedules.
      • Ability to work in a self-driven, performance/results oriented, fast paced matrix environment Excellent communication, writing, sense of urgency, teamwork, and presentation skills.
      • Strong interpersonal skills required to work with teams in different functions and organizations.
      • Demonstrated ability to effectively work in cross functional teams, meet deadlines, and prioritize multiple projects.
      • Detail oriented with excellent verbal and written communication skills.Working Conditions:
        • This position requires up to 20% of travel (as required).BMSCART#LI-ONSITEGPS_2025If 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.Uniquely Interesting Work, Life-changing Careers
          With 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.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.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS 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/Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.W e're creatinginnovative medicines for patients fighting serious diseases. We're also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.
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