Responsibilities

The Medical Device Manufacturing Talent Pool will use correct product specifications and assembly procedure/work instructions to assemble medical device components, following detailed work instructions and specifications. They will also conduct in-process inspections to ensure assembled devices meet quality standards and specifications, follow the master production schedule, and work with standards and regulations as outlined in the Quality Management System (QMS) documentation. Furthermore, they will adhere to all regulatory and company standards, including FDA regulations, ISO 13485, and Good Manufacturing Practices (GMP).