Full Job Description
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.
Division: Biologics – Molecular and Analytical Development (MAD).
Bristol-Myers Squibb is a global BioPharma company firmly focused on its Mission to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. BMS delivered 14 new medicines to patients in the past 10 years. Innovation is critical for successfully executing our BioPharma strategy. Bristol-Myers Squibb's pipeline is one of the most innovative in the industry. Our pipeline includes a number of biologics products such as YERVOY®, ORENCIA®, NULOJIX®, and a number of exciting clinical stage compounds including anti-PD1 mAb. We embrace a diverse workforce and inclusive culture. The health, safety, professional development, work-life balance and equitable, respectful treatment of our employees are among our highest priorities.
The Associate Scientist position within the Impurities group in the Analytical Method Development organization has the opportunity to drive the application and implementation of analytical methods for Host Cell Protein (HCP) preparation, identification, and quantitation during clinical product development of biologics in BMS pipeline. This position reports to the Impurities Method Development Group Leader, within the Biologics Development organization of BMS Global Manufacturing and Supply (GMS) division.
Responsible for performing development and validation work for qPCR and ELISA methods.
Write method development, qualification/validation protocol and reports, method procedures and technical transfer reports
Maintain laboratory notebook and record keeping under GxP compliance and guidelines
Participate in departmental initiatives.
BS in related discipline with a minimum of 2-4 years relevant experience
MS in related discipline with 0-2 years relevant experience
Proficient with variety of bioanalytical techniques, specifically qPCR and ELISA based assays.
Experienced in the use of SoftMax software.
Proficient with analytical instrument operation, maintenance troubleshooting and software programming
Excellent communication and interpersonal skills, both written and verbal required.
Job Function : Analytical Development
Primary Location : NA-US-NJ-New Brunswick
Organization : GMS – Biologics - New Brunswick
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.