Documentation Analyst I (Aesthetics Med Device) (Bothell WA)

Documentation Analyst I supports GMP/regulatory documentation for an aesthetics medical device, administers Agile Change Order, Manufacturing Change Order, and Deviation processes, coordinates with other disciplines to ensure documentation is complete and compliant, leads change review meetings, maintains physical document control records (e.g., DHRs), performs administrative Agile tasks (user management, monthly metrics, quality audits), ensures documentation complies with GMP and regulatory requirements, assists in development and revision of Agile processes, and collaborates in a regulated, team-based office environment.