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Bristol-Myers Squibb

Scientist, Analytical Development

Bristol-Myers Squibb, New Brunswick, New Jersey, us, 08933


Scientist, Analytical Development Scientist, Analytical Development

Apply locations New Brunswick - NJ - US time type Full time posted on Posted 7 Days Ago job requisition id R1587910 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 rich in diversity. 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. Position:

Scientist

Location : New Brunswick, NJ

Drug Product Development (DPD) Our Drug Product Development team is committed to CMC design, development, and commercialization of innovative drug products to improve patient lives. We leverage the best people, collaboration, and cutting-edge innovation to achieve this commitment. BMS’s internal engine of innovation includes unrivaled industry leading expertise in CMC development of small molecules, protein biotherapeutics, protein degraders, and other therapeutic modalities. We collaborate closely with our colleagues in R&D and Commercial to design our drug products. Position Summary We are seeking an analytical scientist with a passion for designing and performing analytical studies across an increasingly complex portfolio of small molecules and biologics at all stages of development. As an individual contributor this role will be responsible for the execution and interpretation of analytical and bioanalytical measurements for drug development candidates and providing guidance to drug product development teams. This position entails collaborative interaction with multidisciplinary teams across Product Development to ensure awareness of current advanced technologies and instrumentation capabilities. Key Responsibilities The Scientist will collaborate as an individual contributor within a drug product project matrix team. The selected candidate will support drug product formulation and process development. Analyze drug candidates to determine chemical and biophysical properties utilizing advanced analytical chromatographic techniques. Develop fit-for-purpose analytical methods to support drug product development. Conduct characterization, investigation, and troubleshooting to provide key insights and understanding for drug product CQA assessment. Independently analyze, review and document analytical data in compliance with regulatory requirements and generate timely and concise documentation of scientific results. Work with multidisciplinary teams to resolve challenges encountered in drug development through experimental design and execution. Champion lab safety and lab organization. Qualifications & Experience Required: Strong fundamental knowledge of analytical separation science for synthetic, peptide, or nucleic acid molecules. Demonstrated laboratory experience in using analytical techniques (HPLC/UPLC, UV-Vis) for the analysis of synthetic, peptide or nucleic acid molecules. Experience using other analytical techniques such as LC/MS or electrophoretic techniques a plus. Demonstrated problem solving skills and strong desire to grow scientifically. The ability to collaborate and work effectively with individuals and as part of cross-functional teams. Ability to execute and document scientific experiments and effectively communicate study results. Ideal Candidates Would Also Have: Experience performing quantitative analysis or in-vitro release measurements of nanoparticle, liposome, long acting injectable, and other novel sterile product drug delivery technologies. Knowledge of dissolution or biorelevant dissolution testing and the biopharmaceutical classification system. Other Qualifications: PhD in Analytical Chemistry or a related field with 0–2 years of post-doctoral or industry experience, MS with 2–4 years, or BS with 5–7 years of relevant experience. Development Value: The Scientist will have interdepartmental responsibilities with regards to participating in workgroups, cross-functional teams, implementation/execution, and cultural initiatives. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

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