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Associate Scientist
Quality Control Flow Cytometry
Posted on 8/3/2022
INACTIVE
Locations
Summit, NJ, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Management
R
Writing
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
  • Anticipate and troubleshoot problems
  • Recommend corrective actions and participate in development of best practices
  • 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
  • Work and communicate effectively within the team to ensure timelines are met
  • 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 review in accordance with required release timelines
  • Communicate effectively with peers, and demonstrate teamwork, with regards to results of review and corrections required
  • 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 related tasks
  • Perform assigned tasks within a CAPA, deviation, or project
  • 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
  • Bachelor's degree, in a Science preferred
  • 3-5 years of relevant work experience, preferable in a regulated environment
  • Cell Therapy Experience is highly preferred
  • Hands on experience with various bioanalytical techniques including ELISA, qPCR and FACS
  • Some prior Knowledge and Working experience with Flow Cytometry is a Plus
  • Ability to accurately and completely understand, follow, interpret and apply Global
  • Technical writing skills
  • 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
  • Ability to communicate effectively with peers, department management and cross- functional peers
Bristol-Myers Squibb

10,001+ employees

Biopharmaceutical development company
Company mission
Bristol-Myers Squibb engages in the discovery, development, licensing, manufacturing, marketing, distribution and sale of pharmaceuticals.