Test Technician

Techlink Systems Inc.; Saint Paul (MN); On-site; USD 30,000 - 47,000; Full time

Job summary

Techlink Systems Inc. in Saint Paul, MN is seeking a Test Technician to support the production of high-quality medical device instruments onsite.

Under general supervision, you will assemble and test electronic components and finished devices in a controlled manufacturing environment. You will use automated test equipment, read engineering drawings, document findings, and help maintain Device History Records to ensure traceability and regulatory compliance.

Qualifications

• Experience with electronic assembly and testing in a medical device industry.
• High School Diploma or equivalency is required.
• 2+ years experience with electromechanical assemblies/electronic manufacturing preferred.

Responsibilities

• Performs testing of electronic components and assemblies using automated test equipment
• Documents findings in a readable timeless format
• May perform mechanical assembly of electromechanical subassemblies and devices
• Reads and interprets engineering drawings, schematics and complex test procedures.
• Maintains accurate records to ensure Device History Records and quality documentation.

Skills

Electronic assembly

Test equipment

Reading schematics

Documentation

Education

High School Diploma

Tools

Automated Test Equipment

Job description

Job Title: Test Technician
Location (On-site, Remote, or Hybrid?): St. Paul, MN (onsite)
Contract Duration: Contract until 05/14/2027
Working hours: 8a - 4:30p
Total hours: 40

Job Summary:

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

Job Responsibilities:

• Performs testing of electronic components and assemblies using automated test equipment
• Documents findings of investigation in a readable timeless format
• May perform mechanical assembly of electromechanical subassemblies and devices
• Ability to read, comprehend and follow written procedures; understand and follow verbal instructions. May instruct others in the use of all manuals, test procedures and documentation associated with specialized equipment.
• Reads and interprets engineering drawings, schematics and complex test procedures.
• Participates in continuous improvement/quality initiatives in order to enhance production processes to 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 the quality of all products.
• 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 SOP's, equipment, policies and procedures, including any department specific requirements.
• Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

Minimum Qualifications:

• Experience with electronic assembly and test in a medical device industry preferred.
• High School Diploma or equivalency is required
• 2 or more years experience with electromechanical assemblies/electronic manufacturing, technical certifications, etc. preferred"