Job Description
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: careers.bms.com/working-with-us . 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 Senior 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: Lead and manage bioassay development workstreams including planning, prioritization and delivery of key program milestones. Serve as a technical lead for bioassay development activities supporting early and late-stage development programs. Design, develop and implement fit-for-purpose potency and biological characterization assays including assay qualification/validation. Independently perform experimental design, execution, data analysis, and documentation. Author and review technical reports, protocols, and method documentation. Contribute to sections of regulatory submissions and responses as appropriate. Contributes to and drives development of the analytical control strategy and anticipates and addresses technical, regulatory, and other business needs Collaborate effectively with stakeholders across Discovery, Development, Quality, and Commercial organizations to ensure alignment and high-quality deliverables. Lead technical discussions and present data in cross-functional forums to influence project direction and decision-making. Generate and thoroughly document results and maintain instrumentation in a GMP-compliant environment. Mentor and provide technical guidance to junior scientists and contribute to a culture of scientific excellence, innovation and continuous improvement. Qualifications : PhD in immunology, cell biology, molecular biology or equivalent field with 2-4 years' experience, or MS with 4-6 years' experience, or BS with 7-9 years' relevant experience. Typically, 3+ years directly applicable experience in biopharmaceutical development. Demonstrated expertise in cell-based assay development for assessment of protein function and structure/function relationships. Experience in optimization of ELISAs; Experience in BIACORE, FACS or automation or advanced data analysis is highly desirable. Proven ability to work independently on complex technical problems and apply sound scientific judgment Excellent interpersonal, communication, and collaboration skills in a matrixed, cross-functional environment. Solid understanding of regulatory, compliance, and GMP guidelines applicable to analytical development. 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: $117,170 - $141,986 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.