Build and manage an integrated Master Transfer Plan spanning sending and receiving sites, running phase gates from readiness, validation, launch, and stabilization
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 compliance with local regulations, corporate standards, and industry best practices, including ISO 13485 and FDA 21 CFR 820 requirements.
Matching Summary
Build and manage an integrated Master Transfer Plan spanning sending and receiving sites, running phase gates from readiness, validation, launch, and stabilization.
Skills & Requirements
Must-have
integrated Master Transfer Plan
product transfer and ramp-up
process/equipment validation strategy
GMP, EHS, and regulatory compliance
medical device manufacturing experience
Nice-to-have
common set of values
customer success focus
collaboration and conflict resolution
coaching ability
international travel up to 60%
Key Requirements
Bachelor’s degree in engineering, Project Management, or related field
Minimum 8–10 years of project management experience
PMP/Prince2 or equivalent preferred
Lean/Six Sigma credentials preferred
Proven track record in managing product/process/equipment transfers