Scientist Custom Process Analytics

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At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

Bristol Myers-Squibb is developing clinical-stage, novel cellular immunotherapies based on two distinct and complementary platforms - Chimeric Antigen Receptors (CARs) and T Cell Receptors (TCRs) technologies. Our goal is to revolutionize medicine by re-engaging the body's immune system to treat cancer.

We are recruiting a scientist to join the Custom Process Analytics (CPA) team of our Cell Therapy Analytical Development (CTAD) organization in Warren, NJ. The ideal candidate will work with a talented and experienced team to enable the rapid advancement of cellular therapy products from pre-clinical development through commercialization. The successful candidate should have experience in the development and implementation of analytical methods for cell therapy product characterization, including flow cytometry, molecular biology, and implementation of method automation and new technologies. The incumbent will provide custom method development and routine sample testing in support of cell therapy process development and method characterization activities. In addition, demonstrated leadership of teams of lab scientists would be a plus. This position will report into the head of CPA.

Responsibilities will include, but are not limited to, the following:


Direct technical and laboratory activities focused on custom analytical method development.
Lead and coordinate routine sample testing activities in support of process development studies. This includes; sample management, test scheduling, method support and related laboratory activities.
Provide scientific and technical guidance, and serve as SME for flow cytometry, cell quantification, molecular (qPCR) and/or ELISA analytical capabilities.
Ensure robust data acquisition, analysis, integrity and reporting in an efficient and timely manner.
Balance resource allocation based on project priorities.
Communicate effectively to staff, key partners, and stakeholders in a rapid and efficient manner.
Collaborate with other departments within the larger Process & Analytical Development (P&AD) organization.
Provide scientific guidance to development operations, clinical, and commercial QC teams. Maintain current awareness of GMP/GTP and other regulations, guidance documents, advisory committees, industry standards and trends that are applicable to current and future Cell Therapy Development operations and products.


Skills/Knowledge Required :


PhD in cell biology, immunology, molecular biology, or related discipline with 3 year R&D / analytical development experience, or MS with 10 years R&D / analytical development experience in a relevant field.
Extensive technical experience in flow cytometry and molecular biology methodologies
Experience with high-volume, rapid, routine sample testing, is preferred
Management experience preferred, with demonstrated ability to develop and lead scientific staff.
Familiarity with and constant attention to the evolving landscape through literature review/publication, conference attendance, industry working group leadership, etc.
Strategic thinker with excellent problem solving and conflict resolution skills.
Ability to foster a strong team-first environment with the ability to lead multiple projects.
Demonstrated success in leading high performing analytical development teams.


Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.

Company: Bristol-Myers Squibb

Req Number: R1527145_EN

Updated: 2020-07-08 00:00:00.000 UTC

Location: Warren,New Jersey

Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.

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