Test Technician

Working under general supervision, this position is responsible for the production of high-quality medical device instruments, including detailed assembly and testing of various electronic components and finished devices in a controlled manufacturing environment. Supports all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.

Title: Operator I
Location: St. Paul, MN 55117
Duration: 6 Month Contract with possible extension
Shift: 8:00 AM to 4:30 PM
Payrate: $21.42/hr

Job Summary
Working under general supervision, this position is responsible for the production of high-quality medical device instruments, including detailed assembly and testing of various electronic components and finished devices in a controlled manufacturing environment.

Key Responsibilities

• Performs testing of electronic components and assemblies using automated test equipment.
• Documents findings of investigation in a readable, timely format. (source said "timeless" flagging in case it should be "timely")
• May perform mechanical assembly of electromechanical subassemblies and devices.
• Reads, comprehends, and follows written procedures; understands and follows verbal instructions. May instruct others in the use of manuals, test procedures, and documentation associated with specialized equipment.
• Reads and interprets engineering drawings, schematics, and complex test procedures.
• Participates in continuous improvement and quality initiatives to enhance production processes and achieve quality and profitability metrics.
• Maintains accurate records to ensure Device History Records and quality documents are accurate, all parts are traceable, and quality issues can be addressed to assure product quality.
• Prioritizes work by determining the sequencing and timing of different jobs based on precedence and importance.
• Positively represents the company during tours by demonstrating techniques and sharing appropriate information.
• Supports all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
• Complies with U.S. Food and Drug Administration (FDA) regulations, ISO or other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
• Adheres to all environmental, health and safety SOPs, equipment, policies and procedures, including any department-specific requirements.
• Maintains positive, cooperative communication and collaboration with all levels of employees, customers, contractors, and vendors.

Minimum Qualifications

• High School Diploma or equivalency (required).
• 2+ years of experience with electromechanical assemblies / electronic manufacturing; technical certifications preferred.
• Experience with electronic assembly and test in the medical device industry preferred.