Senior Scientist, Quality Control Analytical Testing

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. Read more: careers.bms.com/working-with-us The QC Senior Scientist is responsible for supporting the analytical testing at QC Analytical Testing department at the Cell Therapy Operations (CTO) manufacturing facility during clinical and commercial phases for Sun-Wed AM shift. This department is responsible for flow-cytometry and molecular based testing for stability, validation, critical reagent qualification, training, and other critical support as needed. This includes the ability to interface with multiple groups, the ability to independently perform tasks, interpret results, and troubleshoot. Shift Available: Sunday to Wednesday 8 a.m. – 6 p.m. Responsibilities: Perform testing on critical reagent and stability samples. Utilize scientific principles to assist in analytical testing methods and the proper use of laboratory equipment. Perform cell based in-vitro flow experiment, ELISA, qPCR to assess critical reagent concentration. Capable of handling complex issues and solving problems with only general guidance. Prepare and present continuous improvement projects to management. Comprehensive understanding of regulatory guidelines and can independently develop, write, and execute methods, protocols, reports and other related documents. Complete all work in a timely manner. Perform peer review of testing data. Review all data in accordance with applicable procedures and cGMP requirements. Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner. Complete all reviews in accordance with required release timelines of reagents Communicate effectively with peers, and demonstrate teamwork, with regards to results of review and corrections required. Train new analysts to general job duties. Complete necessary training to become a qualified trainer. Perform training effectively. Document training per procedural and cGMP requirements. Support document revision, project, CAPA, and investigation/deviation tasks. Perform assigned tasks within a CAPA, deviation, or project. Participate in complex projects and continuous improvement efforts. Take a leadership role, as required, for projects. Draft and review technical documents, such as SOPs and protocols/reports. Communicate effectively with management regarding task completion, roadblocks, and needs. Demonstrate initiative, courage, and continuous improvement throughout investigation/corrective action lifecycles. Knowledge & Skills: Advanced hands-on experience with various analytical techniques including flow-cytometry, molecular techniques and scientific knowledge in the characterization and transfer of pharmaceutical products. Advanced ability to accurately understand, follow, interpret, and apply global regulatory and cGMP requirements. Advanced technical writing skills, problem-solving ability/mentality, technically adept and logical thinking. Ability to represent the interests of the group on cross-functional teams. Ability to work independently in a high-paced team environment, meet deadlines, and prioritize work from multiple projects. Ability to work with management locally and globally. Advanced ability to communicate effectively with peers, department management and cross-functional peers. Basic Requirements: Bachelor’s degree required, preferably in science. Advanced degree preferred. 3-5 years of hand-on flow cytometry analytical testing. Preferred Requirements: Master’s Degree in a science field preferred. 5 years of cGMP analytical testing. Demonstrated experience working with polychromatic flow-cytometry panels, flow-cytometry data analysis, ELISA and qPCR preferred. Working Conditions: The incumbent should be able to distinguish colors and possess correctable vision to 20/20, annual eye exam is required. The incumbent must analyze numerical values on a daily basis. The incumbent will be working a laboratory setting up to six (6) hours per day. The incumbent will be working around biohazardous materials, including chemical agents up to six (6) hours per day. BMSCART,
LI-Onsite 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. Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture. To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S. Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.