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Specialist, Assistant Engineer
- Bristol Myers Squibb (Warren, NJ)
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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
We are looking for a driven and talented individual to join our team in advancing the development of cutting-edge cell therapy processes and products-from early-stage research through to commercial manufacturing. In this hands-on, laboratory-based role, you will play a key part in shaping the future of T cell therapy by:
+ Characterizing and optimizing multiple unit operations to ensure the production of safe, effective, and high-quality drug products.
+ Integrating innovative technologies into the manufacturing workflow to enhance efficiency, scalability, and robustness.
+ Solving complex platform challenges and aligning cross-functional strategies to support a unified and forward-looking development approach.
You will collaborate closely with multidisciplinary teams across the organization to design and refine robust, scalable manufacturing processes that meet the highest standards of quality and performance.
Responsibilities will include, but are not limited to, the following
Design and execute development and characterization studies for autologous and/or allogeneic cell therapy unit operations, driving innovation in cellular process development. Analyze and interpret experimental data using statistical tools and methodologies; clearly communicate insights through presentations and technical discussions. Manage and maintain comprehensive experimental datasets across multiple studies, ensuring accuracy, consistency, and accessibility. Document experimental work promptly and thoroughly in electronic laboratory notebooks, adhering to best practices and regulatory standards. Author detailed technical reports summarizing experimental design, execution, and outcomes to support internal decision-making. Draft and revise technical documentation to facilitate seamless technology transfer and support cross-functional collaboration. Support manufacturing investigations, including deviations and CAPAs, by providing technical expertise and process insights. Contribute to extended characterization efforts for clinical materials, ensuring timely and high-quality data generation to support product development.
Skills/Knowledge Required
+ Bachelor's degree in Biochemical, Chemical, or Biomedical Engineering, or a related biological science discipline.
+ Foundational knowledge of CAR-T cell therapy and its applications in clinical and commercial settings.
+ Hands-on experience with mammalian cell culture and aseptic techniques, demonstrating strong technical and experimental laboratory skills.
+ Ability to apply engineering principles and statistical tools-including Design of Experiments (DoE)-to guide study design and process optimization.
+ Highly driven with a strong desire to learn and grow; capable of working independently with minimal supervision.
+ Exceptional ability to manage time, prioritize tasks, and handle multiple projects simultaneously in a fast-paced environment.
+ Excellent verbal and written communication skills, with the ability to clearly convey complex technical information.
+ Proven track record of working effectively in cross-functional teams, meeting deadlines, and contributing to shared goals.
+ Willingness to support occasional weekend work as needed to maintain ongoing experiments
The starting compensation for this job is a range from $63,000 - $79,000,
plus incentive cash and stock opportunities (based on eligibility). The starting pay rate takes into account characteristics of the job, such as required skills and the geographic location where work is performed. Final, individual compensation is decided commensurate with demonstrated experience. For more on benefits, please visit our BMS Careers Site. Eligibility for specific benefits listed therein may vary based on job and location.
Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.
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.
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 Protocol
BMS 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 [email protected] . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) 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.
**Company:** Bristol-Myers Squibb
**Req Number:** R1592301
**Updated:** 2025-06-06 04:55:49.770 UTC
**Location:** Warren-NJ
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
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