Senior Analyst, Technical Product Management Lab Workflow Systems (signals)
Johnson & Johnson
Beerse, Belgium
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Revvity signals platform
Fair data principles
Laboratory operations
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Johnson & Johnson is seeking a Senior Analyst in Technical Product Management for its Lab Workflow Systems in Beerse, Belgium. The role focuses on enhancing laboratory operations through data-driven solutions and requires a strong background in pharmaceutical development, data analytics, and stakeholder collaboration.
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Job Summary
Harness the power of data, technology, predictive modeling, and informatics to inform decisions and enable a digital enabled organization that speeds up life-saving treatment development.
Focus on the Revvity Signals platform and play a pivotal role in the development, deployment and life cycle management of FAIR data solutions that enhance laboratory operations and life cycle management.
Collaborate with scientists, engineers, and IT teams to optimize manufacturing systems, ensuring seamless data integration and usability, while managing vendor relationships and supporting regulatory compliance.
Matching Summary
Match Score: 75
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Johnson & Johnson is seeking a Senior Analyst in Technical Product Management for its Lab Workflow Systems in Beerse, Belgium. The role focuses on enhancing laboratory operations through data-driven solutions and requires a strong background in pharmaceutical development, data analytics, and stakeholder collaboration.
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Skills & Requirements
Must-have
Revvity Signals platform
FAIR data principles
laboratory operations
drug development process
GMP regulations
Nice-to-have
digital transformation
creative problem-solving
cross-functional leadership
global end-to-end attitude
benchmarking industry best practices
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
Experience in Synthetics Pharmaceutical Development is preferred
Hands-on experience with Revvity Signals is preferred
Proven experience with the drug development process
Hands-on experience with advanced data analytics
Demonstrated knowledge of Good Manufacturing Practice (GMP) regulations