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 transfer and validation.
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
cross functional meetings
process transfer activities
equipment installation and validation
GMP, EHS, and regulatory compliance
manufacturing processes across multiple products
Nice-to-have
culture that unifies and embraces uniqueness
customer success focus
collaboration and conflict resolution
coaching ability
Key Requirements
Bachelor’s degree in engineering, Project Management, or related field
8–10 years of experience in project management
Proficiency with PM tools (e.g., MS Project, Smartsheet)
PMP/Prince2 or equivalent preferred
Lean/Six Sigma credentials preferred
Proven track record in managing product/process/equipment transfers in medical device manufacturing
Leadership in Quality, RA, Manufacturing, Facilities, and Supply Chain in Medical Devices is an advantage