Sr Sci Data Sciencesenior Analyst, Technical Product Management Lab Workflow Systems (biovia Onelab)

Johnson & Johnson UK

Beerse, Belgium
On-site
Biovia onelab platform expertise
Fair data principles
Drug development process
Johnson & Johnson is seeking a Senior Analyst, OneLab Subject Matter Expert for their Digital Operations & Strategy team in Beerse, Belgium. The role emphasizes data lifecycle management, collaboration with scientific experts, and driving digital transformation within pharmaceutical development

Job Summary

  • The Senior Analyst, OneLab Subject Matter Expert plays a pivotal role in the development, deployment and life cycle management of FAIR data solutions that enhance our laboratory operations.
  • Your expertise will support our strategic digital transformation initiatives, ensuring data integrity, accessibility, and data usability across the organization.
  • The successful candidate will be a proactive and effective problem solver who is intellectually curious and has a strong interest in data and how it supports the development of innovative, life-saving treatments.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Senior Analyst, OneLab Subject Matter Expert for their Digital Operations & Strategy team in Beerse, Belgium. The role emphasizes data lifecycle management, collaboration with scientific experts, and driving digital transformation within pharmaceutical development.

Skills & Requirements

Must-have

  • Biovia OneLab platform expertise
  • FAIR data principles
  • drug development process
  • advanced data analytics
  • Good Manufacturing Practice (GMP) regulations

Nice-to-have

  • digital transformation and innovation
  • fast-paced, dynamic environment
  • interpersonal and communication skills
  • strategic thinker
  • cross-functional teamwork

Key Requirements

  • Bachelor’s degree or higher in Chemical Engineering, Chemistry, Pharma or related sciences/engineering disciplines
  • Minimum of 8 years of relevant industry experience
  • Hands-on experience with Biovia OneLab is preferred
  • Proven experience with the drug development process
  • Demonstrated knowledge of Good Manufacturing Practice (GMP) regulations

Work Rights

Not specified

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