Quality Technician IV

About the role

We are seeking a skilled individual to join our team as a Quality Engineer. This role is responsible for developing and maintaining automated inspection equipment programs, applying GD&T to inspection test methods, troubleshooting production issues, and ensuring data integrity.

Responsibilities

• Develops automated inspection equipment programs to meet drawing specifications.
• Applies GD&T to inspection test methods.
• Maintains qualification and calibrations on automated inspection equipment.
• Works with equipment manufacturers to schedule maintenance and service activities on equipment.
• Troubleshoots production problems and performs root cause analysis on equipment, fixtures, inspection methods and parts.
• Ensures data integrity of inspection methods from the inspection equipment into InfinityQS.
• Stays current on new technology and innovations on the leading edge of automated inspection.

Requirements

• Minimum of 8 years of relevant experience.
• High school diploma or equivalent (United States), vocational or technical education or certification (all other countries).
• Experience with CMM Programming, Zeiss Calypso, Hexagon PCDMIS, vision inspection equipment, and previous drafting and inspection experience.
• Advanced experience in medical device or other regulated manufacturing environments.
• Experience supporting investigations, root cause analysis, CAPA, and audit readiness.
• Strong understanding of FDA, ISO 13485, GMP, or similar quality/regulatory standards.
• Ability to analyze quality data and identify trends or improvement opportunities.
• Experience mentoring peers or serving as a technical resource across teams.

Qualifications

• To be considered for this role, please ensure the minimum requirements are evident in your applicant profile.

Skills

• Must have experience with CMM Programming, Zeiss Calypso, Hexagon PCDMIS, vision inspection equipment, and previous drafting and inspection experience.
• Advanced experience in medical device or other regulated manufacturing environments.
• Experience supporting investigations, root cause analysis, CAPA, and audit readiness.
• Strong understanding of FDA, ISO 13485, GMP, or similar quality/regulatory standards.
• Ability to analyze quality data and identify trends or improvement opportunities.
• Experience mentoring peers or serving as a technical resource across teams.

Benefits

At Medtronic, we offer a competitive salary and a comprehensive benefits package including:

• Health, Dental, and Vision Insurance
• Health Savings Account
• Healthcare Flexible Spending Account
• Life Insurance
• Long-term Disability Leave
• Dependent Child Care Spending Account
• Tuition Assistance/Reimbursement
• Employee Stock Purchase Plan
• Employee Assistance Program
• Non-qualified Retirement Plan Supplement (subject to IRS earning minimums)
• Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums)

The following benefits and additional compensation are available to all regular employees:

• Incentive plans
• 401(k) plan plus employer contribution and match
• Short-term disability
• Paid time off
• Paid holidays

Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan.