Senior Supplier Quality Engineer - ISO 13485/Audit Lead

Laborie Medical Technologies Corp; Maple Grove (MN); On-site; USD 95,000 - 125,000; Full time

Benefits offered by this job

Paid time off

Medical insurance

Dental insurance

Vision insurance

HSA contributions

401k match

Parental leave

Wellness programs

Job summary

Laborie Medical Technologies Corp in Minnesota is seeking a Senior Supplier Quality Engineer to manage product quality through supplier evaluation procedures, risk management, and vendor audits. You will identify and mitigate supplier risks, participate in supplier selection and monitoring, and ensure compliance with quality systems and material specifications.

The role requires a Bachelor's in engineering and 8+ years in QA, with expertise in ISO 13485 and 21 CFR, strong leadership, and

Qualifications

• Bachelors' degree in engineering or related field with 8+ years in QA.
• Expertise with ISO 13485 and 21 CFR compliant quality systems.
• Proven leadership and auditing experience across internal/external audits.

Responsibilities

• Maintain and implement supplier evaluation procedures.
• Use risk management tools to identify and mitigate supplier risks.
• Participate in supplier selection and monitoring.
• Audit suppliers for quality system and material specification compliance.

Skills

Leadership

Auditing

ISO 13485

21 CFR compliance

Statistical methods

Risk management

Vendor evaluation

Quality assurance

Education

Bachelor's degree in engineering or related scientific field

Tools

Quality Management System

Risk Assessment Tools

Workflow Automation

Vendor Auditing

Job description

Laborie Medical Technologies Corp in Minnesota is seeking a Senior Supplier Quality Engineer to manage product quality through supplier evaluation procedures, risk management, and vendor audits. You will identify and mitigate supplier risks, participate in supplier selection and monitoring, and ensure compliance with quality systems and material specifications.

The role requires a Bachelor's in engineering and 8+ years in QA, with expertise in ISO 13485 and 21 CFR, strong leadership, and