Quality Technician- 1st Shift

Quality Technician – 1st Shift

Location:

MN Facility 0HR, Lakeville, MN, US

Salary Range: $30.00 To $35.00 Hourly

EPTAM Precision Micro‑Machining is looking for a Quality Technician – 1st Shift to join our team in Lakeville, MN. Join us as we create medical devices that support our OEM partners in creating life‑saving parts and positive outcomes for their patients.

EPTAM Precision Micro‑Machining is a world‑class manufacturer specializing in precision manufacturing of custom medical device components for original device manufacturers. We have established a strong reputation in providing custom implantable components across orthopedic, spine, cardiovascular, vascular, endovascular, and pelvic health sectors. Our operations support the Robot Assisted Surgery (RAS) and Minimally Invasive Surgery (MIS) industries, as OEMs look for partners for the future of advanced interventions.

Our facility, compliant with FDA and ISO 13485 standards, is celebrated for its high‑quality system and standards. Our culture of quality, combined with seamless collaboration between Engineering, Quality, and Manufacturing Operations, allows us to deliver the very best to employees, customers, and the world.

Benefits Include:

• Professional Development/On the Job Training
• Health and Wellness Benefits
• Clean, Friendly, Safe work Environment
• Recognition and Rewards Program
• Tuition Re‑imbursement
• Competitive Pay/Merit Increases
• 401k with Company Match
• Employee Assistance Program (EAP)

1st Shift: Monday through Friday 6:00am to 2:30pm

The Quality Technician is primarily responsible for performing inspections in accordance with documented procedures to ensure compliance with customer requirements and the Quality Management System (QMS). The role supports a controlled and efficient inspection flow and contributes to continuous improvement efforts related to inspection processes, systems, and procedures.

• Adhere to all QMS requirements, documented procedures, and company policies
• Identify, document, and communicate deviations, non‑conformances, and quality issues; support containment and segregation of non‑conforming products
• Assist with root cause investigations, corrective actions, and continuous improvement initiatives
• Perform inspections including First Article, startup, in‑process, receiving, and final inspections in accordance with applicable procedures and standards
• Verify product conformance, including dimensions, visual characteristics, labeling, traceability, and purchased material requirements
• Execute sampling inspections and collect accurate inspection data to support SPC, trend analysis, and quality reporting
• Operate, set up, and program advanced inspection equipment (e.g., CMM, vision systems)
• Maintain calibration status awareness and support calibration activities, including verification of tool readiness before use
• Ensure proper handling, storage, and maintenance of inspection equipment, fixtures, and accessories
• Complete assigned tasks, special projects, and other duties as directed by management
• Measure components using advanced measuring equipment and hand gages such as calipers and micrometers
• Communicate professionally with coworkers and respond appropriately to feedback from supervisors

• Represent the company during customer, internal, and ISO audits, as well as FDA inspections
• Support communication that ensures management and employee understanding of current good manufacturing practices (cGMP)
• Leverage industry practices and apply them to internal systems and processes
• Support training of personnel on inspection methods; ensure training is documented per procedures
• Coordinate inspection priorities with the Quality Manager in alignment with production schedules
• Assist in development, revision, and implementation of inspection procedures and related quality documentation
• Provide feedback to improve inspection processes, methods, and overall quality system effectiveness
• Understand the sensitivity of the data handled by systems under your control and take appropriate measures to protect it

• Education: High School diploma or GED. Associate degree, vocational training, or equivalent combination of education is preferred, but not required.
• Experience: 3+ years relevant quality assurance experience or training, or equivalent combinations of education and experience. Internships and part‑time experience acceptable. Experience with in a manufacturing, medical device company or other similarly regulated manufacturing environment preferred.
• Licenses, Certifications and/or Registrations: Industry recognized Quality certification(s) preferred but not required.

ADP
1507