Manufacturing Planner - Scheduler III
Core
Manage engineering documentation, CAD drawings, and maintenance records for a GMP-regulated manufacturing facility.
Role type
Facilities Engineering Documentation Specialist
Builds
Engineering documentation, as-built drawings, and maintenance records for pharmaceutical/biotech facilities
Domain
Life Sciences / GMP Manufacturing
Required skills
Engineering documentation management, CAD (AutoCAD), Electronic Document Management Systems (EDMS), CMMS, cGMP compliance, regulatory inspection support, project coordination, facility walkdowns
Preferred skills
Adept Document Management System, Blue Mountain/BMRAM, deviation/CAPA/change control processes, contractor drawing review, process improvement
Technologies
AutoCAD, Adept, Blue Mountain/BMRAM, Microsoft Office
Responsibilities
Maintain GMP As-Built and Non-GMP Master Drawings, coordinate CAD activities and drawing revisions, perform field walkdowns to verify installed conditions, support CMMS activities and work orders, manage EDMS workflows for document routing and archival, support regulatory inspections by retrieving engineering documentation
Seniority
Mid-level, hands-on IC