Associate Scientist / Senior Associate Scientist Full-time NEW

Associate Scientist / Senior Associate Scientist

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.

Job Summary

The Genomics Analytical Development (GAD) group is seeking an enthusiastic, self-driven Associate Scientist or Senior Associate Scientist to pioneer the development of analytical methods in support of engineered T-cell programs. The ideal candidate will possess robust technical skills, complemented by a strong foundation in molecular biology, viral vectors, and gene editing.

If you are excited to take on new challenges in a fast-paced and dynamic environment, this role offers the opportunity to drive impact. The successful candidate will be responsible for analytical method development, sample and critical reagent management, and testing to enable the process development and characterization of viral vectors and engineered T-cell products.

Primary Responsibilities

• Method Development: Design and develop analytical methods to characterize lentiviral/AAV vectors, vector-related processes, and on-/off-target genome modifications in engineered T cells.
• Method Life Cycle: Perform phase-appropriate validation, transfer, and bridging of analytical methods, including the training of additional laboratory operators.
• Laboratory Execution: Design and execute complex experiments to support process development.
• Sample & Reagent Management: Oversee sample management, execute routine testing, and manage critical reagents to support ongoing programs.
• Compliance & Documentation: Maintain accurate, meticulous electronic laboratory notebooks (ELN) and author technical, developmental, and regulatory documents (e.g., study reports, SOPs).
• Collaboration: Partner with team members to support day-to-day laboratory operations, ensuring a smooth, safe, and efficient working environment.
• Communication: Present experimental designs, data, and findings at internal and external meetings.

Basic Qualifications

• B.S. in Molecular Biology or a related biological science discipline with 2+ years of post-graduate research experience, OR an M.S. in Molecular Biology or a related field.
• Proficiency in molecular biology techniques (e.g., construct design and cloning, primer/probe design, qPCR, RT-PCR, ddPCR).
• Strong hands-on experience with mammalian cell culture and cell manipulation (transfection and transduction).
• Proven ability to strictly adhere to existing methods/SOPs while also possessing the critical thinking skills to design and troubleshoot complex experiments.
• Exceptional documentation skills with the ability to generate meticulous experimental records, study reports, and SOPs.
• Excellent time management skills with the capacity to prioritize tasks across multiple projects in a deadline-driven environment.
• Strong sense of responsibility, accountability, integrity, and the ability to mentor or train additional operators.

Preferred Qualifications

• 2+ years of biotechnology or pharmaceutical industry experience in assay development or related fields.
• Hands-on experience with lentiviral infectious titer assay.
• Hands-on experience with qPCR and droplet digital PCR (ddPCR).
• Working knowledge of Electronic Laboratory Notebook (ELN) systems and DNA sequence analysis software.

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:

Seattle – WA: $82,750 – $100,271

The 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 Off
• US 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 holidays
• Based 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 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.

Supporting People with Disabilities

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