Specialist, QC Analytical

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.

At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.

The Specialist, QC Analytical is responsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. May assist with method transfer, documentation, deviations, investigations, and continuous improvement efforts.

Shift Available:

• Wednesday - Saturday, Onsite Day Shift, Flexible 7 a.m. - 5 p.m.

Responsibilities:

• Perform routine testing of in-process, final product, and stability samples.

• Perform testing for method transfer/validation/verification.

• Perform data verification, data review and review of GMP documentation for general methods.

• May perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.

• Train analysts on general job duties.

Knowledge & Skills:

• Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.

• Knowledge of LIMS, ELN and laboratory data analysis systems preferred.

• Problem-solving ability/mentality, technically adept and logical.

• Ability to communicate effectively with peers, department management and cross-functional peers.

• Experience with writing technical documents preferred.

• Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.

Basic Requirements:

• Bachelor's degree or equivalent required, preferably in science. An equivalent combination of work experience may be considered.

• 2+ years of relevant analytical testing.

• 1 year of QC experience in a manufacturing regulated environment (cGMP).

• Strong pipetting skills.

• 1 year of any of the following techniques: Flow Cytometry, qPCR, or ELISA.

Preferred Requirements:

• Prior experience with using a Quality Management System (QMS).

• Prior experience with authoring or revising documents.

• Prior experience working on quality records (ex. CAPAs and Deviations).

• Prior experience with data review on peers.

BMSCART, #LI-Onsite

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.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has a diverse occupancy structure that determines where an employee is required to conduct their wo