Quality Data Scientist

Location
Devens, MA, United States
Posted
Sep 25, 2020
Ref
R1527108
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.

Summary:

Coordinate and provide oversight for the planning of QC demand for Quality Control

Responsibilities:
  • Partner with all Quality functional areas for department capacity planning, electronic time capture (eTime), data gathering analysis for department.
  • Gather and analyze metrics for Quality department to support governance forums (quality council, investigation review board, Tier boards, etc.).
  • Leads key Quality forums and/or is a standing member in escalation/inform meetings.
  • Provides oversight to QC lab samples to ensure adherence to testing is completed on-time to meet customer needs.
  • Resolves Capacity issues (minor equipment and labor issues) in QC Operations scheduling based on the consolidated Stability, Supply and Production scheduling priorities & updates the schedule accordingly.
  • Develops priority lists based on demand requirements, taking in account products in re-analysis, analytical methods, QC labor and equipment constraints.
  • Provides customer updates on testing status, in accordance with the QC lab.
  • Evaluates impact of schedule changes, and communicates to stakeholders.
  • Coordinates and facilitates activities that lead to test completion and QA disposition completion, in partnership with QC lab.
  • Monitor the performance metrics for the assigned products (i.e. quality attainment).
  • Pro-actively suggests opportunities for improvement.


Qualifications:
  • Bachelor's Degree and 4+ years of experience in a biopharmaceutical GLP or GMP environment
  • Basic knowledge of Good Manufacturing Practices (GMP).
  • Must have strong organizational skills and the ability to work as part of a cross functional team.
  • Ability to prioritize objectives from multiple projects, adhere to scheduled timelines while maintaining flexibility and attention to detail.
  • 2+ years of work-related experience in production planning, and/or in quality control/quality assurance, and/or in project management is preferred.
  • Proficient in common computer software applications, experience with LIMS and ELN computer applications is preferred.
  • Professional (APICS) certification (CPIM, CPM or CIRM) is preferred.


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.