
• Performed in-process inspection of components and assemblies to verify quality conformance.
• Assembled medical devices according to Federal QSR, ISO 13485, lot history records, manufacturing instructions, standard operating procedures, and safety policies.
• Recorded information on lot history records and perform component accountabilities.
• Set-up and operate manufacturing equipment.
• Maintained clean room standards, practices, and housekeeping according to standard operating procedures and the illness and injury prevention program.
• Cleaned supplies and manufacturing equipment and work areas.
• Reported causes of process and/or documentation issues and assist in resolution.
• Responsible for completing personal training records.
• Adhered to the Company's Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures.
• Ensured other members of the department follow the QMS, regulations, standards, and procedures.
• Performed other work-related duties as assigned.