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.

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
  Job Type: Contract
  Pay: $28.00 - $30.00 per hour

Benefits:

• Flexible schedule
• Health insurance
• Life insurance
• Paid time off

Experience:

• Performs testing of electronic components and assemblies: 3 years (Preferred)
• electronic assembly and test in a medical device industry: 3 years (Preferred)
• electromechanical assemblies/electronic manufacturing: 3 years (Preferred)
• biomedical Technician/Medical Device technician: 3 years (Preferred)

Ability to Commute:

• Minneapolis, MN 55442 (Preferred)

Work Location: In perso

• Performs testing of electronic components and assemblies using automated test equipment
• 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.