Data Analyst

Company:
Location: Boudry, NE

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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.

PREREQUISITES

Degree in Engineering, Chemistry, Pharmacy or Natural Science.; experience in pharmaceutical industry and in GMP validation activities are considered an asset.

Introduction:

pMS&T is a science-driven organization dedicated to building in-depth and comprehensive knowledge of our OSD products and their processes. We work across the entire lifecycle of our Pharmaceutical Products and across both internal and external manufacturing and API Manufacturing.

The Product Robustness Analyst is supporting the development and implementation of strategies that ensure Global Commercial Supply is maintained in a constant state of compliance for the good of our patients. More specifically, the Product Robustness Analyst partners with other pMS&T functions to design and execute procedures that guarantee the manufacturing robustness at internal and external sites.

Responsibilities will include, but are not limited to the following:

  • Support the implementation of structures, tools, and processes to actively manage process performance/robustness across the BMS Pharma portfolio.
  • Contribute to ensure that new pharma products are launched with an appropriate level of robustness, in collaboration pMS&T functions and Manufacturing site.
  • Design and execute procedures that enable an efficient collection of data (possibly in real time) from the different unit operations in line with the defined control strategy.
  • Support analysis of data and draw up robustness boards.
  • Contribute to the issuing of Continued Process Verification protocols and reports.
  • Prepare protocols and reports that enable execution of experiments or Technical Batches.
  • Support the completion of investigations led by Swiss pMS&T by issuing documents or reports.
  • Interface with multiple sites and departments (i.e., Engineering, Facilities, Manufacturing, Regulatory Affairs, Quality Control and Quality Assurance) to accomplish predefined goals.
  • Support pMS&T groups to develop project plans for validation activities and ensure results are delivered in a timely manner.

Skills/Knowledge Required:

  • Degree in Engineering, Chemistry, Pharmacy or Natural Science.
  • Experience in pharmaceutical industry and in GMP validation activities are considered an asset but not mandatory.
  • Ability to work well as an integral part of a large Project Team.
  • Ability to work across organizational boundaries.
  • Good written and verbal communication and interpersonal skills.
  • Good command of English and preferably another European language.

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.

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