Scientist, Analytical Development Full-time NEW

Scientist, Analytical Development

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.

Position Summary

This Scientist position is based in New Brunswick, NJ. The role supports analytical development for Bristol Myers Squibb's expanding biologics pipeline. The successful candidate supports biologics analytical development through the design, implementation, and operation of automation, modeling, and artificial intelligence (AI) approaches to enable more efficient, robust, and cost-effective workflows. These technologies and best practices will be transferred across functional areas, including clinical and commercial analytical and quality groups. The role also supports characterization and method development across early- and late-stage biologics programs via digitization capability, helping to modernize analytical workflows and improve throughput and data insights. This position offers the opportunity to work in a dynamic, highly collaborative environment, with potential to lead development activities and contribute to cross-functional, matrixed teams.

Key Responsibilities

• Design, develop and deploy assay and data automation solution, part of the team to design and deploy analytical data modeling, and AI-enabled technologies for clinical analytical development, and support technology transfer to commercial analytical organizations.
• Program, operate, and troubleshoot automated analytical/data platforms to improve efficiency and reproducibility.
• Collaborate with automation specialist and digital teams to enable automated data capture and data integrity.
• Evaluate and implement novel analytical platforms and automated technologies to enhance capability, robustness, and assay performance.
• Support the develop biochemical methods as needed for biologics drug substance and drug product clinical release testing, stability studies, and characterization.
• Build and maintain strong collaborative relationships with Research, Process technology development, and Quality Control (QC) groups.
• Maintain state-of-the-art scientific knowledge; present findings at internal and external forums; publish results; and author technical and regulatory documentation.
• Sustain a safe, compliant, and high-performance laboratory environment.
• Support planning and execution of internal and external events.

Qualifications

The successful candidate will have:

• A Ph.D. in Chemical/Biochemical Engineering, Bioengineering, Analytical Biochemistry, Analytical Chemistry, Biotechnology, or a related discipline with 0-2 years of relevant industry and/or academic experience. Alternatively, a Master's degree in one of these fields with a minimum of 2-4 years of relevant industry and/or academic experience. Bachelor's degree with 5-7 years' experience can be considered.
• Hand-on experience on laboratory automation and liquid handling platforms (e.g., Tecan, Hamilton); capable of coding assay automation scripts.
• Experience or demonstrated understanding on modeling, and/or AI-based technologies.
• Familiarity with biologics analytical techniques for antibodies, antibody–drug conjugates, and RNA lipid nanoparticles (LNPs), including HPLC, UPLC, capillary electrophoresis, isoelectric focusing, FFF, MALS, and DLS.
• A basic understanding of biologics process development.
• Proficiency with Empower, SYMYX ELN, Microsoft Office applications, and data analysis tools.
• Working knowledge of statistical experimental design and data analysis.
• Self-starter, strong communication, and organizational skills.
• Ability to work effectively and collaboratively in a team-oriented environment.

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:

New Brunswick – NJ – US: $100,330 – $121,571

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: The 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.