Bristol Myers Squibb Company

Quality Control Molecular Scientist Cell Therapy

Summit West, NJ, United States
Sep 05, 2020
Required Education
Bachelors Degree
Position Type
Full time
At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.


The Scientist is responsible for supporting Quality Control bioanalytical testing for release of clinical and commercial products. This includes the ability to interface with multiple groups, the ability to independently perform tasks, interpret results, and troubleshoot. Additionally, when needed, this position will be able to assist with training and assay development, validation & transfer.

REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities:
  • Advanced hands on experience with various analytical techniques including ELISA, qPCR, FACS and scientific knowledge in the characterization and transfer of pharmaceutical products.
  • Advanced ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
  • Advanced technical writing skills.
  • Advanced problem-solving ability/mentality, technically adept and logical.
  • Ability to represent the interests of the group on cross-functional teams.
  • Ability to set priorities of the group and manage timelines.
  • Ability to work with management locally and globally.
  • Advanced ability to communicate effectively with team members, department management and cross- functional peers.

Education and Experience:
  • Bachelor's degree required, preferably in Science.
  • Advanced Degree preferred.
  • 5-8 years of relevant Quality Control work experience, in the pharmaceutical industry required.
  • Knowledge of GMP Regulations required.
  • Experience working in an Aseptic Manufacturing environment is highly preferred.
  • An equivalent combination of education and experience may substitute.
  • Ability to work extended hours, occasional weekends and holidays.

Duties and Responsibilities:

Perform testing of in-process, final product, and stability samples.
• Utilize scientific principles to assist in analytical testing methods and the proper use of laboratory equipment.
• Capable of handling complex issues and solving problems with only general guidance.
• Prepare and present continuous improvement projects to management.
• Comprehensive understanding of regulatory guidelines and can independently develop, write and execute methods, protocols, reports and other related documents.
• Complete all work in a timely manner and focus on Right First Time (RFT).

Perform peer review of testing data.
• Review all data in accordance with applicable procedures and cGMP requirements.
• Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner.
• Complete all reviews in accordance with required release timelines.
• Communicate effectively with peers, and demonstrate collaborative teamwork, with regards to review of results.

Train new analysts to general job duties.
• Complete necessary training to become a qualified trainer.
• Perform training effectively.
• Document training per procedural and cGMP requirements.

Support document revision, project, CAPA, and investigation/deviation tasks.
• Complete assigned tasks within a CAPA, deviation, or project on time
• Participate in complex projects and continuous improvement efforts.
• Take a leadership role, as required, for projects.
• Draft and review technical documents, such as SOPs and protocols/reports.
• Communicate effectively with management regarding task completion, roadblocks, and needs.
• Demonstrate initiative, courage, and continuous improvement throughout investigation/corrective action lifecycles.

Performs other tasks as assigned.

  • The incumbent should be able to distinguish colors and possess correctable vision to 20/20, annual eye exam is required.
  • The incumbent must analyze numerical values on a daily basis.
  • The incumbent will be required to work in a laboratory setting for extensive periods of time ranging from 4 to 10 hours per day.
  • The incumbent must be flexible to work in a rotating weekend holiday/schedule.
  • The incumbent will be working with and around biohazardous materials, including chemical agents.


Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.