Associate, Quality Control, Cell Therapy

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.

Purpose and Scope:

The primary focus of the Associate I, Quality Control (QC) role will be to perform GMP testing to support product release and in-process testing. This role will also provide technical support and troubleshooting for analytical or microbiological tests.

This is for a Sun-Wed 6AM to 430PM Shift

Knowledge, Skills, and Abilities:

Education:

• Bachelor’s Degree or equivalent combination of education and experience

Experience

• 0-2+ years of regulated industry experience or equivalent combination of education and experience

Responsibility:

• Perform GMP lot release and in-process testing for analytical and/or microbiological test methods and perform data analysis using various electronic instruments and computer systems
• Support assay transfer and method validation by executing validation protocols and generating data/results to support the final report
• Assist in the implementation of new assay methodologies and the associated instruments
• Operate and maintain analytical and/or microbiological instruments according to standard operating procedures
• Participate in cross-functional assay training
• Author and revise standard operating procedures and test methods
• Identify and facilitate continuous improvement projects
• Lead small scope projects

The starting compensation for this job is a range from $65,000 – $82,000, plus incentive cash and stock opportunities (based on eligibility).

The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed. Final, individual compensation will be decided based on demonstrated experience. 

Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit our BMS Careers Site.

Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, 
pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). 
Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like 
tuition reimbursement and a recognition program.

WORKING CONDITIONS (US Only):

The role is set in a controlled environment where the analyst will don personnel p