Scientist

The Scientist role is a technical expert supporting the Cellular Therapy product portfolio. Successful candidates will have a strong foundation in designing and conducting experiments at the laboratory bench, analyzing data, and interpreting results in molecular biology methods. This role will perform hands‑on laboratory experiments in support of QC analytical methods. Responsibilities Provide molecular biology analytical expertise in support of QC lab investigations and method optimizations. This encompasses supporting technical investigations to identify root cause and provide corrective and preventive actions, including method remediations and experimental studies at the bench. In accordance with established protocols and research objectives, independently execute experimental work with a high degree of technical proficiency, contribute to data analysis and documentation, and collaborate within cross‑functional teams. Contribute to the development and optimization of new and existing laboratory methods and protocols. Present experimental findings and progress updates to immediate team. Support the preparation of internal technical reports and presentations as appropriate. Support transfer of commercial methods and method validation in compliance with global regulatory requirements. Responsible for the stewardship of molecular methods in the Cell Therapy Quality organization. Implement method lifecycle and method maintenance programs to support molecular biology methods in support of cell therapy drug products. Author, revise, and review technical documents such as test methods, SOPs, trend reports, and/or investigation reports as appropriate. May lead project, CAPA and deviation/ investigation related tasks and/or continuous improvement efforts. May provide support in the authoring of the analytical sections of regulatory submissions, responding to health authority questions and functioning as the method validation and method transfer expert during inspections as required. May partner with development organizations in the design of development and qualification studies, selection and characterization of reagents, and method optimization initiatives. Perform other tasks as assigned. Reporting Relationship This position will report to Cell Therapy Global Quality Analytical Sciences and Technology (ASAT) management. Qualifications Bachelor's degree in relevant scientific discipline or equivalent is required. Advanced degree preferred. 6 years of relevant analytical experience or equivalent combination of education and experience, preferably in a regulated environment (GMP), cellular therapy, or gene therapy. Strong scientific background and expertise, encompassing various cell‑therapy relevant methodologies. Molecular Biology: Molecular methodologies including those related to lentiviral, AAV vectors and other gene delivery platforms. Specifically expertise in DNA extraction and qPCR. Hands‑on laboratory experience and demonstrated proficiency with standard laboratory techniques relevant to the role. Experience in analytical method lifecycle including method transfer, validation, critical reagents and maintenance. Experience providing training in method execution as well as instrument operation and standardization. Experience in cGMP regulations and application within the Quality Control environment. Onsite/Hybrid 100% Onsite Work Schedule M-F; Standard Hours! Equal Opportunity Employer and does not discriminate against employees or applicants based on race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability, veteran status, or any other classification protected by federal, state, or local laws. #J-18808-Ljbffr Bristol Myers Squibb