Job Summary

• Build and manage an integrated Master Transfer Plan spanning sending and receiving sites, running phase gates from readiness, validation, launch, and stabilization.
• Lead process transfer activities from sending sites to the receiving site, ensuring minimal disruption and excellent quality assurance.
• Ensure transfer deliverables satisfy ISO 13485 and FDA 21 CFR 820 requirements.

Matching Summary

Skills & Requirements

Key Requirements

• 8-10 years project management experience
• Bachelor's degree in engineering or related field
• PMP/Prince2 or equivalent preferred
• Lean/Six Sigma credentials preferred
• Experience in medical device manufacturing

Work Rights