Sr. Associate Scientist, Gene Editing Process Development

  • Bristol Myers Squibb
  • Seattle, Washington
  • Full Time

Working with Us
Challenging. Meaningful. Life-changing. Those arent 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. Youll 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 .

Key Responsibilities

  • Plan and execute PD studies for optimizing the production of nucleic acids
  • Characterize the functional properties of nucleic acids in genomic editing applications
  • Maintain and process primary human T cells, including thawing, passaging, and cryopreservation.
  • Plan and execute experiments to optimize GERM formulations for non-viral delivery to T cells
  • Organize and maintain GERM inventories, and related quality data, for distribution across the Seattle site
  • Analyze data and effectively communicate experimental results to research scientists and maintain proper documentation of experimental results, including ELN entries and development reports.
  • Assist in identifying GERM pCQAs from literature and in-house biophysical characterization

Basic Qualifications

  • M.S or B.S. in Biochemistry, Molecular Biology, Bioengineering, Chemical Engineering, or related disciplines
  • 5-8 years of industry experience in process development and/or gene editing-related development
  • Independently motivated with the ability to multitask and work in teams.
  • Desire and drive to learn the biological mechanism of cell and gene therapy products
  • Ability to communicate clearly and concisely through oral presentation and technical writing

Preferred Qualifications

  • Demonstrated ability to use scientific literature and other resources to generate and test hypotheses
  • Previous experience with in vitro mammalian cell culture and proper aseptic technique
  • Background in CRISPR-based technology and/or chemically synthesized RNA oligonucleotides
  • Familiarity with purification processes for in vitro produced nucleic acids (chromatography, TFF, dialysis, etc.)
  • Familiarity with basic analytical assays used for assessing gene editing (e.g., ddPCR, ELISA, CGE, NGS etc.)
  • Experience with statistical analysis and experimental design using JMP

The starting compensation for this job is a range from $91 ,830 - $111,300, 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.

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 Years 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 doesnt 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 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:

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Job ID: 488709886
Originally Posted on: 8/8/2025

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