Quality Inspector - 1st Shift

Quality Inspector 1st Shift

EPTAM Precision Micro-Machining is looking for a Quality Inspector 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 in is a world-class manufacturer specializing in precision manufacturing of custom medical device components for original device manufacturers. We've established a strong reputation in providing custom implantable components across various medical sectors, including orthopedic, orthopedic spine, cardiovascular, vascular, endovascular, and pelvic health sectors. Our manufacturing operations support the Robot Assisted Surgery (RAS) and Minimally Invasive Surgery (MIS) industries, as OEM's 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 ingrained culture of quality, combined with seamless collaboration between Engineering, Quality, and Manufacturing Operations, allows us to deliver the very best to our employees, customers, and the world.

EPTAM Solutions, our parent company with locations nationwide, is at the Heart of Manufacturing. We recognize our parts touch lives, and our teams assume this responsibility with vigor. Our minds never sleep. Join our incredible team at any one of our locations and reap the benefits of an employee focused company. We excel at what we do for our customers, our employees, 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 w/ Company Match
• Employee Assistance Program (EAP)

SHIFT DETAILS:

1st Shift

Monday through Friday 6:00am to 2:30pm

POSITION SUMMARY: The Quality Inspector is primarily for the following:

Perform inspection of parts and perform calibrations to ensure conformance with customer specifications and regulatory requirements.

ESSENTIAL FUNCTIONS: Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

Report any potential product or process deviation or non conformance per QMS requirements to Leads and the Quality team.

Inspect parts and perform calibrations to ensure conformance with customer specifications and regulatory requirements.

Assist with and perform floor audits.

Operate, calibrate, and assist with maintenance of vision and inspection equipment

Document inspection results and maintain accurate, complete records.

Read and interpret blueprints, engineering drawings, and specifications to confirm operations meet production standards.

Ensure quality activities align with the production schedule.

Use precision measurement tools (micrometers, calipers, gauges) to verify product dimensions and tolerances.

Employees must be able to relate to other people beyond receiving instructions. Can get along with co-workers or peers and respond appropriately to feedback from a supervisor in a professional manner.

OTHER RESPONSIBILITIES:

Represent the company, as required, during customer audits, internal audits, ISO audits, and FDA inspections.

Cross train and assist other operational departments to support the production schedule as needed.

Maintain Good Manufacturing Practices (GMPs) with strong emphasis on safety.

Train and mentor other employees in quality procedures, inspection methods, and equipment use as assigned.

Identify and recommend improvements within the Quality System or production processes.

Perform accurate data entry and review documentation for completeness and correctness.

Execute high quality work while following all Quality Management System (QMS) requirements.

Understand the sensitivity of the data managed by systems under your control and take appropriate measures to protect it.

EDUCATION AND EXPERIENCE:

EDUCATION: High School diploma or general education degree (GED). Associate degree, vocational training, or equivalent training/experience preferred, but not required.

EXPERIENCE: 2+ year(s) relevant quality experience or training or demonstrated ability to execute the Essential Functions for this position. Internships and PT experience acceptable. Experience within a manufacturing, medical device company or other similarly regulated manufacturing environment preferred.

LICENSES, CERTIFICATIONS AND/ REGISTRATIONS: Industry recognized Quality certification(s) preferred, but not required.