Global Labeling Project Manager – Onsite Sunnyvale

Maxonic Inc.

Sunnyvale (CA)

Vor Ort

USD 102.000 - 146.000

Vollzeit

vor 7 Stunden
Sei unter den ersten Bewerbenden

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Zusammenfassung

Maxonic is seeking a Project Manager 3 Global Labeling in Sunnyvale, CA to lead labeling programs for medical devices. You will plan, execute, and oversee cross-functional labeling projects across geographies, ensuring regulatory alignment and on-time delivery.

The role requires a four-year engineering degree, 5+ years in the medical device field, and strong collaboration with Regulatory, Manufacturing, Quality, and IT teams. Onsite work with travel about 10% is expected.

Qualifikationen

  • Bachelor's degree in engineering or equivalent.
  • 5+ years in the medical device field.
  • Experience in global multi-discipline environment (Regulatory, Manufacturing, Quality, IT, Logistics).
  • Strong written and verbal communication for internal/external stakeholders.
  • Proven ability to manage labeling projects and timelines.
  • Willingness to travel ~10% domestically and internationally.

Aufgaben

  • Manage labeling projects for product development and global rollout.
  • Develop, plan, and execute labeling programs ensuring regulatory alignment.
  • Coordinate with cross-functional teams and external vendors.
  • Lead process improvements using Six Sigma and/or Agile methodologies.
  • Prepare reports and communicate project status to stakeholders.

Kenntnisse

Project management
Global labeling
Regulatory compliance
Cross-functional teamwork
Communication
Problem solving
Leadership
Travel willingness

Ausbildung

Bachelor's degree in Engineering

Tools

Tableau
Smartsheet
Microsoft 365
SAP

Jobbeschreibung

Maxonic is seeking a Project Manager 3 Global Labeling in Sunnyvale, CA to lead labeling programs for medical devices. You will plan, execute, and oversee cross-functional labeling projects across geographies, ensuring regulatory alignment and on-time delivery.

The role requires a four-year engineering degree, 5+ years in the medical device field, and strong collaboration with Regulatory, Manufacturing, Quality, and IT teams. Onsite work with travel about 10% is expected.

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