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, including equipment installation, validation, and workforce onboarding.
Ensure transfer deliverables satisfy ISO 13485 and FDA 21 CFR 820 requirements and drive process/equipment validation strategy.
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
process transfer activities
equipment de-install, crating/shipping
operational readiness
process/equipment validation strategy
GMP, EHS, and regulatory compliance
international travel up to 60%
Nice-to-have
culture that unifies
embraces uniqueness
customer success focus
collaboration and conflict resolution
coaching ability
Key Requirements
Bachelor’s degree in engineering, Project Management, or related field
Minimum 8–10 years of project management experience
Medical device manufacturing environment experience
Proficiency with PM tools (e.g., MS Project, Smartsheet)