Sr. Research Associate

Profile

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

This Sr. Research Associate position will work in Biologics Downstream Process Development group in Summit, New Jersey and will focus on biologics downstream process development and be responsible for the development of scalable purification process, process characterization, Tox material production, and tech transfer to GMP facilities for clinical/commercial manufacturing. The successful applicant should be a highly-motivated and collaborative individual with strong technical and organizational skills. The position represents an excellent growth and learning opportunity, will work closely with experienced scientists in a fast-paced and

highly collaborative environment.

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


Execute harvest and downstream processing of biologics produced in mammalian cell culture or microbial cell culture.

Routinely perform protein purification and sample analysis in support of process development of biologics.

Work collaboratively with other functional groups such as cell line, upstream and analytical development to accomplish project goals and milestones.

Perform routine lab activities including buffer preparation, column packing and sample submission.

Use creative problem-solving skills to troubleshoot experimental challenges.

Detail-oriented tracking and documenting of experimental results in laboratory notebooks and databases.

Analyze, summarize, and present experimental results to manager and other team members.


Skills/Knowledge Required:


Knowledge and/or experience with downstream process development including chromatography, filtration, AKTA FPLC systems (particularly unicorn software).

Familiar with HPLC/UPLC, spectrophotometry, SDS-PAGE and Western-blot assays.

Outstanding critical thinking and organizational skills, lab notebook practices, and attention to details.

Good verbal and written communication skills.

Demonstrated ability to function in a collaborative/team-oriented R&D environment.

Able to communicate and connect with all levels of the organization.


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 the resources to pursue their goals, both at work and in their personal lives.

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, disability or protected veteran status.

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