Scientist, Bioassay 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. Read more:

Scientist, Bioassay Development - Potency and Impurity Analytical Development

Our Biologics Development team is responsible for development and transfer of safe, efficient, and approvable biologics drug substance manufacturing processes and analytical methods for all of BMS' biologics portfolio. We work closely with other BMS units to support our clinical pipeline through to late stages of clinical development. Innovation is at the core of what we do, with an intense focus on efficiency, speed, robustness, and approvability of our processes and methods.

Here, you'll get the chance to grow and thrive through opportunities uncommon in scale and scope, pursue innovative ideas, and advance professionally alongside some of the brightest minds in Biopharma

Description:

Bristol Myers Squibb is the world leader in Biotherapeutics for Immuno-Oncology. The Potency and Impurity Analytical Development (PIAD) department is the global center for biological potency assay development, biological characterization and clinical lot release. To enable the continuous expansion of our biologics pipeline, we are looking for experienced professionals passionate about bringing recombinant therapeutics to patients to address significant unmet medical need.

The Scientist, Bioassay Development has the opportunity to drive state-of-the art potency assay development that supports the company's portfolio of preclinical and clinical- stage biologics. The role requires a strong understanding of cell biology/immunology/molecular biology and expertise with the design and development of cell-based assays to assess protein function. The role calls for close collaboration with early discovery groups, process sciences groups, internal analytical functions, as well as with Commercial Analytical Science & Strategy and the Quality Control organization.

Responsibilities:

* Directly accountable for bioassay development for early and late-stage development programs, development of fit-for-purpose biological characterization assays, assay qualification/validation, and strong collaboration with stakeholders in partner organizations.

* Responsible for experimental design, execution, data review and analysis, document writing, and contributing to sections of regulatory submissions.

* Participates in development of the analytical control strategy and anticipates and addresses technical, regulatory, and other business needs

* Generate and thoroughly document results and maintain instrumentation in a GMP-compliant environment.

* Inspires innovation and operational excellence and fosters a continuous learning environment.

Qualifications:

* Ph.D. in Immunology, Cell Biology, Molecular Biology, or a related field with 0-2 years of experience; or M.S. with 2-4 years of relevant experience; or B.S. with 5-7 years of relevant experience.

* Typically, 0-2+ years directly applicable experience in biopharmaceutical development.

* Strong technical knowledge of cell-based assay development.

* Experience with using cell-based assays to assess protein structure/function relationships.

* Experience in ELISAs

* BIACORE, FACS or automation experience would be advantageous.

* Methodical, and committed to high-quality results.

* Strong interpersonal and communication skills.

* Awareness of regulatory and compliance guidelines.

#LI-Onsite

#GPSProd Dev

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…