Assembler III 3rd shift

Essential Duties and Responsibilities: Support company goals and objectives, policies and procedures, Good Manufacturing Practices, and FDA regulations including compliance to EN ISO 13485, Medical Device Quality Standards. Comply with company Standard Operating Procedures (SOPs) and departmental policies and procedures (DOPs), objectives, the quality assurance program, as well as safety and environmental standards. Ability to establish, build and maintain professional working relationships with all levels of staff, clients, and suppliers. Excellent interpersonal, verbal, and written communication skills. Meticulous attention to detail and meeting deadlines. Ability to learn new equipment and processes, and quickly demonstrate proficiency in their and interpret manufacturing procedures, engineering drawings, and inspection procedures and comply with their requirements. All documents are written in English. Demonstrates accuracy, thoroughness and monitors own work to ensure quality. Practice and always advocate good safety skills.

Education and Experience: 5 years related industry experience in medical device production assembly.5 years of experience in a medical device environment Experience in FDA/GMP/ISO environment preferred Excellent interpersonal, verbal, and written communication skills. Meticulous attention to detail Wears personal protective equipment as required.