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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 rich in diversity. 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.
Title: Assistant Scientist, Vector Volume Determination Testing
Location: Seattle, WA
The Assistant Scientist, Vector Volume Determination Testing position is a hands-on, laboratory-based role in the Vector Volume Determination Testing group. The candidate will execute critical vector performance testing procedures in support of engineered T-cell programs, commercial and clinical manufacturing. This role will require high quality work and timely output in a cell therapy GMP laboratory environment.
This role will transition to a team within the Cell Therapy Development (CTD) organization after the vector testing function has been sunset mid- to late-2025. In this function, the candidate will support the design and execution of experiments, analysis of results, and communication of conclusions across teams. The candidate must be able to work independently as well as with guidance from a manager and demonstrate good written and oral communication skills. The candidate will gain functional knowledge of laboratory equipment, closed system cell culture techniques and valuable exposure to the industry standards of clinical and developmental CAR-T manufacturing.
Key Responsibilities:
Perform routine cell culture experiments per written procedures in a GMP setting, where ability to recognize deviation from accepted practice is required
Assist with the revision and creation of process documents, such as SOPs and electronic work instructions
Collaborate with others to coordinate day-to-day lab activities to ensure smooth operation
Maintain laboratory space to comply with regulatory requirements and safe work environment
Work in teams through continual interaction with internal and external teams throughout the production process to exchange information regarding the run(s) in process
Design and execute experiments with supervision to assess new processing technologies and determine process parameter design space
Complete timely and thorough documentation of electronic laboratory notebooks
Critically analyze and interpret data using statistical methods
Organize, record, and maintain large experimental data sets
Communicate study findings across multiple departments
Qualifications & Experience:
B.S. in Chemical/Biological Engineering, Immunology, Biology, or relevant scientific discipline with 0-3 years of biotechnology or cell therapy industry experience
Demonstrated proficiency in aseptic processing of mammalian or primary cell culture in biological safety cabinet is required
Experience working in, or exposure to, GMP setting, especially using Good Documentation Practices, is required
Excellent documentation and data management skills
Detail oriented with excellent verbal and written communication skills
Demonstrated ability to thrive on a team in a fast-paced environment, and prioritize work across multiple projects
The starting compensation for this job is a range from $77,960 - 94,500, 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 where the job is performed. 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 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.
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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 an inclusive culture, promoting diversity 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 a diverse 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/
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