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Senior Specialist,Quality Control Analytical Testing - Summit West, NJ

Job in Summit, Union County, New Jersey, 07901, USA
Listing for: National Guard Employment Network
Full Time position
Listed on 2026-07-17
Job specializations:
  • Healthcare
    Data Scientist
  • Science
    Data Scientist
Job Description & How to Apply Below

QC Senior Scientist

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.

PURPOSE AND SCOPE OF POSITION:

The QC Senior Scientist is responsible for supporting the analytical testing at QC Analytical Testing department at the CAR T manufacturing facility during clinical and commercial phases. 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.

REQUIRED COMPETENCIES (Knowledge, Skills, and Abilities):

  • 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.
Position Requirements
10+ Years work experience
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