Bristol-Myers Squibb
Associate, QC Analytical, Cell Therapy
Bristol-Myers Squibb, Summit, New Jersey, us, 07902
Associate, QC Analytical, Cell Therapy
Working with UsChallenging. 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.The Associate position is responsible for performing testing of in-process, final product, and stability samples in accordance with BMS policies, standards, procedures, and Global Regulatory and cGMP requirements to support the Quality Control Analytical department in the Bristol Myers Squibb (BMS) CAR T Manufacturing facility located in Summit, NJ. The candidate may also support data verification and GMP documentation review as needed.Shift Available:Wednesday - Saturday, Onsite Afternoon Shift, 4 p.m. - 2 a.m.Responsibilities:Perform routine testing of in-process, final product, and stability samples.May review GMP documentation and perform data verification.Support document revision, project, CAPA and deviation/ investigation related tasks and/or continuous improvement efforts.May train analysts on general job duties.Perform other tasks as assigned.Knowledge & Skills:Ability to accurately and completely understand and follow procedures.Apply scientific principles to analytical testing and the proper use of laboratory equipment.Ability to communicate effectively with peers and management regarding task completion, roadblocks, and needs.Attention to detail and demonstrated organizational skills.Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.Basic Requirements:Bachelor's degree preferred in science. Associates degree with equivalent combination of education and work experience may be considered.0-2+ years of relevant analytical testing or QC experience.Prior pipetting skills (1 mL).Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.Prior experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, aseptic technique).If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles.
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Working with UsChallenging. 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.The Associate position is responsible for performing testing of in-process, final product, and stability samples in accordance with BMS policies, standards, procedures, and Global Regulatory and cGMP requirements to support the Quality Control Analytical department in the Bristol Myers Squibb (BMS) CAR T Manufacturing facility located in Summit, NJ. The candidate may also support data verification and GMP documentation review as needed.Shift Available:Wednesday - Saturday, Onsite Afternoon Shift, 4 p.m. - 2 a.m.Responsibilities:Perform routine testing of in-process, final product, and stability samples.May review GMP documentation and perform data verification.Support document revision, project, CAPA and deviation/ investigation related tasks and/or continuous improvement efforts.May train analysts on general job duties.Perform other tasks as assigned.Knowledge & Skills:Ability to accurately and completely understand and follow procedures.Apply scientific principles to analytical testing and the proper use of laboratory equipment.Ability to communicate effectively with peers and management regarding task completion, roadblocks, and needs.Attention to detail and demonstrated organizational skills.Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.Basic Requirements:Bachelor's degree preferred in science. Associates degree with equivalent combination of education and work experience may be considered.0-2+ years of relevant analytical testing or QC experience.Prior pipetting skills (1 mL).Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.Prior experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, aseptic technique).If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles.
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