Senior Analyst, Technical Product Management Lab Workflow Systems (signals)

J&J FAMILY OF COMPANIES

Beerse, Belgium
**
Revvity signals platform
Fair data principles
Laboratory operations
** Johnson & Johnson is seeking a Senior Analyst, Technical Product Management for their Lab Workflow Systems, focusing on the Revvity Signals platform. The role involves data lifecycle management, collaboration with scientific experts, and enhancing laboratory operations to support innovative therapeutic development. **

Job Summary

  • As a key member of the Business System Ownership team, the Senior Analyst, Signals Subject Matter Expert focuses on the Revvity Signals platform and plays a pivotal role in the development, deployment and life cycle management of FAIR data solutions that enhance our laboratory operations and life cycle management.
  • Your expertise will support our strategic digital transformation initiatives, ensuring data integrity, accessibility, and data usability across the organization.
  • We are seeking an enthusiastic and dedicated Senior Analyst, Signals Subject Matter Expert, to join our dynamic team in Beerse, Belgium.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking a Senior Analyst, Technical Product Management for their Lab Workflow Systems, focusing on the Revvity Signals platform. The role involves data lifecycle management, collaboration with scientific experts, and enhancing laboratory operations to support innovative therapeutic development. **

Skills & Requirements

Must-have

  • Revvity Signals platform
  • FAIR data principles
  • laboratory operations
  • data lifecycle management
  • GMP regulations

Nice-to-have

  • digital transformation initiatives
  • intellectually curious
  • creative problem-solving
  • global, end-to-end attitude

Key Requirements

  • Bachelor’s degree or higher
  • Minimum of 8 years of relevant industry experience
  • Experience in Synthetics Pharmaceutical Development is preferred
  • Hands-on experience with Revvity Signals is preferred
  • Proven experience with the drug development process
  • Demonstrated knowledge of Good Manufacturing Practice (GMP) regulations

Work Rights

Not specified

Tailored Resume

Cover Letter