Cfdv
Scientist - Analytical Development
Cfdv, New Brunswick, New Jersey, us, 08933
Primary Location: New Brunswick, New Jersey or Summit, New JerseyThis Analytical Development role will be responsible for developing effective collaborations within Chemical Process Development (CPD) project teams consisting of organic chemists, chemical engineers, and analytical scientists to support an increasingly complex portfolio of small molecules and milla-molecular (ADCs, peptides, oligonucleotides) drug candidates.Responsibilities:Accountable for providing fit-for-purpose analytical methods and analyses which provide key insights and process knowledge for scale-up and process optimization studies for projects within the portfolio.Collaborate within project teams to provide innovative analytical approaches to help solve challenging problems encountered to support route selection and process optimization studies conducted by chemists and chemical engineers.Develop and transfer methods to other analytical release functions to support the timely release of clinical API batches.Partner with other Analytical Functions within CPD, and across Product Development to evolve, integrate and optimize analytical support to create a world-class analytical function.Grow and advance to become either analytical leaders or technical leads for projects within the CPD portfolio.Specific Accountabilities:Willingly and enthusiastically work at the bench to solve analytical challenges encountered within pharmaceutical development. Can be relied upon to work independently to develop and validate methods, as well as investigate and apply innovative separation techniques such as 2DLC or CE.Identify opportunities and/or implement solutions to improve monitoring of continuous manufacturing processes, and increasingly apply automation to improve efficiency, productivity, quality or reduce costs.Actively collaborate with other Key Scientists within the team. Display a can-do attitude and demonstrate the willingness and capability to adapt and grow within a complex and changing environment.Work with leadership to develop self, share best practices, work effectively to solve pharmaceutical development problems, and continuously learn and improve.Qualifications/Requirements:Ph.D. or Masters in analytical or organic chemistry is required. Practical experience directly relevant to the role is critical to success and minimum degree requirements change relative to experience.Experience with chromatographic and/or spectroscopic techniques preferred.Experience in working across matrixed teams highly desirable.Demonstrated commitment to safety.Excellent interpersonal, collaborative, team building, and communication skills to ensure effective collaborations within matrix 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.
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