Sr. Supervisor Training And Doc Control-orthopedics (grecia, Costa Rica)
Johnson & Johnson
Grecia, Costa Rica
Onsite
Document control system
Training program management
Qms compliance
Lead and manage day-to-day document control activities for the QMS, including creation, review, approval, distribution, archival, and obsolescence of controlled documents
Job Summary
Lead and manage day-to-day document control activities for the QMS, including creation, review, approval, distribution, archival, and obsolescence of controlled documents.
Design, implement, and maintain an effective training program tied to QMS documents, job roles, and regulatory requirements.
Partner with cross-functional stakeholders to ensure documentation and training needs are met and aligned with product and process changes.
Matching Summary
Lead and manage day-to-day document control activities for the QMS, including creation, review, approval, distribution, archival, and obsolescence of controlled documents.
Skills & Requirements
Must-have
document control system
training program management
QMS compliance
regulatory requirements
change control processes
Nice-to-have
continuous improvement culture
cross-functional collaboration
people leadership
systems thinking approach
Key Requirements
4 to 6 years' experience
Bachelor's degree in Engineering, Life Sciences, Quality Management, or related field
Demonstrated knowledge of QMS standards and regulations (ISO 13485, 21 CFR Part 820 / FDA QSR)
Experience managing electronic document management and training systems
Proven experience leading projects and/or small teams