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
process transfer activities
equipment de-install, crating/shipping
operational readiness
process/equipment validation strategy
component/tooling transfers
pilot, engineering, and pre-production builds
Nice-to-have
common set of values
culture that unifies
create better solutions
interact with others respectfully
open and honest with one another
do the right things and do things right
Key Requirements
Bachelor’s degree in engineering, Project Management, or related field
Minimum 8–10 years of experience in project management
Medical device manufacturing environment experience
Proficiency with PM tools (e.g., MS Project, Smartsheet, etc.)
PMP/Prince2 or equivalent preferred
Lean/Six Sigma credentials preferred
Proven track record in managing product/process/equipment transfers
Leadership in Quality, RA, Manufacturing, Facilities, and Supply Chain
Strong knowledge of GMP, EHS, and regulatory compliance