Scientist

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.

The Scientist is a member of a core team of experts that provide technical expertise and project leadership on location with one of the company’s external manufacturers of BMS biological products. The Scientist is knowledgeable in drug substance manufacturing processes.

Responsibilities

• Responsible for process fit, technical transfers, process validation, maintenance and continuous improvement of process performance at third party manufacturing and other internal manufacturing facilities.
• Monitoring daily activities at contract manufacturing partner and interfacing with technical and quality representatives at the contract manufacturing site.
• Maintain strong working relationship with external partners.
• Develop and maintain keen technical familiarity with process and process equipment and technical problem solving.
• Prepare, produce, and/or review GMP document, regulatory documents and other technical reports.
• Initiate, conduct or lead investigation into any process excursion and quality events.
• Align and maintain collaborative partnership with internal BMS functions such as Process Sciences, Manufacturing Science and Technology, Analytical Development and Testing, QA, QC, and facilities engineering.·

Required competencies

• B.S in biochemistry, chemistry, biochemical engineering, or a related discipline with 6-8 years of related experience is required.
• An M.S. degree with 2-4 years will also be considered.
• Commercial experience in biologics manufacturing of drug substance is a major plus.
• Direct experience with cGMP protein therapeutic manufacturing.
• High skill level in process development, process scale-up, technical transfers, process troubleshooting, and continuous improvement.
• Working knowledge of regulatory and compliance requirements for biologics.
• Technical writing, computer, and written and verbal communication skills.
• Ability to work effectively as a member of larger cross functional team.
• Experiences in mammalian cell culture recommended.
• Travel up to 20% of the time.
• Fluency in English is required.

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.