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T&O Cytometry QC Research Associate

Bristol Myers Squibb
Seattle 400 Dexter - WA, United States, United Statesfull_timeVerifiedPosted 25 Sept 2025
💰 $92,422/yr($76,270/yr$92,422/yr)

About the role

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. 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 Cell Therapy Thematic Research Center Cancer is one of BMS’s differentiated research platforms delivering innovative therapies to patients. Our mission is to drive leadership in the use of cellular therapies to harness the power of the immune system in treating hematologic malignancies, solid cancers, and autoimmune disease. More specifically, our discovery and translational scientists are focused on developing next-generation, engineered cell-based therapies. The team is committed to discovering and developing transformative therapies that harness the power of the immune system to improve patient outcomes.

In the role as a T&O Cytometry QC Research Associate within Translational Research: Technology & Operations, the ideal candidate:

Primary Responsibilities: Data Quality Control

  • Work primarily on reviewing and performing quality control (QC) of clinical flow cytometry data generated by external partner laboratories, under minimal supervision

  • Utilize data review tools to ensure the quality of flow cytometry data in preparation for downstream analysis

  • Regularly review incoming clinical data to identify and report discrepancies and QC issues

  • Draft and revise standard operating procedures (SOPs) of the data QC process

  • Maintain effective communications with external laboratory partners to facilitate data remediation

  • Collaborate with internal stakeholders to contribute to the development and improvement of data review tools

Additional Laboratory Responsibilities

  • Work in the laboratory under moderate supervision to perform routine sample testing using flow cytometry assay and analyze resulting data

  • Conduct routine maintenance on flow cytometry instruments, troubleshoot issues, and communicate with field application scientists as needed

  • Support critical reagent management, including assay controls, custom antibodies, and frozen samples, ensuring proper handling, storage, and tracking

Other Responsibilities

  • Set and understand priorities in both local and matrixed environments

  • Demonstrate strong teamwork and a collaborative spirit, maintaining networks within and outside the organization

  • Perform other tasks as needed to support team and program objectives

Experience =

Basic Qualifications:

  • Bachelor’s Degree

    • No experience necessary

Preferred Qualifications:  

  • Bachelor’s degree in a relevant scientific field (Immunology, Oncology, Biology) with 0-2+ years of relevant experience

  • Experience with routine clinical sample testing using multi-parameter (8+ colors) flow cytometry assay

  • Strong technical background in flow cytometry and hands-on experience with a broad array of flow cytometry platforms. Experience with Cytek Aurora is a plus.

  • Experience with a variety of flow cytometry analysis software such as BD FACSDiva, FlowJo, FCS Express. Experience with OMIQ is a plus.

  • Experience with LIMS, ELN, and laboratory data analysis system.

  • Strong attention to details and organizational skills.

  • Ability to clearly communicate and operate in a local, and highly matrixed environment.

  • Ability to multitask high priority tasks in parallel with internal and external collaborators.

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

  • Ability to communicate effectively with peers, department management and cross-functional peers about task status, roadblocks and needs.

  • CRO experi

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Company

Bristol Myers Squibb

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