Scientist II Cellular Analytics

Profile

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 II for Cellular Analytics in Cell Therapy Analytical Development organization. S/he will work with a talented and experienced team to enable the rapid advancement of cellular therapy candidates from pre-clinical development through commercialization. (Legacy Celgene equivalency to title of Bioengineer II.)

In addition to proven leadership capabilities, the successful candidate should have experience in the development and implementation of analytical methods for cell analysis, including flow cytometry, as well as assessment and implementation of new technologies. The incumbent will provide strategic direction for the department to establish platform cell analysis strategies, analytical method life-cycle management, and development and implementation of novel technologies. This candidate will report into the lead of Cellular Analytics group which is part of Analytical Development Department.

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


Provide scientific and technical guidance to analytical development programs in support of the development, characterization, qualification, GMP implementation and scale-up of cell analytics methods.
Responsible for carrying out laboratory experiments and analysis for cancer immunotherapy drug product.
Conduct experiments/analysis independently and draw conclusions from data, results with minimal guidance.
Communicate effectively within and across groups. Perform instrument/method troubleshooting within analytical method parameter.
Oversee the design, development, and qualification of analytical methods to assess cellular product identity, purity, quality and potency. Collaborate with other Analytical Development (AD) departments/scientists to ensure the overall analytical strategy is complete and phase appropriate as a member of the AD team.
Coordinate, lead and participate in various aspects of method development, transfer, characterization, investigation and assay validation while collaborating with Cell Therapy Technology, QC, Process Development, Clinical and Commercial Manufacturing, and Quality Operations teams.
Provide scientific guidance to development operations, and clinical and commercial QC teams. Main t ain 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.
Provide key strategic compliance and analytical development input to projects and cross-functional teams, including process development, manufacturing implementation, IMPD and IND preparation, and discussions with regulators.


Skills/Knowledge Required :


PhD/MS in Immunology, Biological Science, Biochemical Engineering, or related discipline with 8-10 yrs. R&D / analytical development experience, or BS with 15 yrs. R&D / analytical development experience in a relevant field.
Established track record of success, sound technical qualifications and depth knowledge in flow cytometry, ELISA, Cell culture. Cell therapy product characterization, method bridging, and other analytical technology experience a plus.
Solid understanding of the fundamentals of assay development, characterization, qualification, and transfer.
Understands cGMP documentation requirements. Skilled in writing and reviewing technical reports.
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 assay 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: R1528104_EN

Updated: 2020-07-24 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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