MedTech Quality Technician — DHR & Process Compliance

Nextern; Maple Grove (MN); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Health Care Plan

Retirement Plan

Paid Time Off

Birthday Holiday

Life Insurance

Family Leave

Disability - Short/Long Term

Taco Thursdays

Job summary

Nextern in Maple Grove, MN, is seeking a compliance-focused professional to ensure production and process control during development and manufacturing of medical devices. You will monitor and train staff, review DHRs, and determine product acceptability with the operator.

The role emphasizes quality documentation, procedures improvement, and collaborative support to the Quality group, with a strong commitment to safety and continuous input.

Qualifications

• Five-year relevant experience desired.
• Working knowledge of quality control standards and testing techniques.
• Excellent verbal and written communication skills.

Responsibilities

• Ensure production and process control compliance during development and manufacturing of medical devices.
• Perform comprehensive Device History Record (DHR) review at close of manufacturing process.
• Decide on handling product issues with operators and determine product acceptability.
• Identify and evaluate procedures to ensure production of quality product.
• Provide technical support to the Quality group as required.
• May write technical reports and other required quality documentation.
• Maintain safe work habits and a clean, safe work area.
• Willing to give/receive constructive input and feedback.

Skills

Quality control standards

Testing techniques

Verbal and written communication

Data interpretation and reporting

Tools

Excel

Word

Outlook

ERP and PLM

Job description

Nextern in Maple Grove, MN, is seeking a compliance-focused professional to ensure production and process control during development and manufacturing of medical devices. You will monitor and train staff, review DHRs, and determine product acceptability with the operator.

The role emphasizes quality documentation, procedures improvement, and collaborative support to the Quality group, with a strong commitment to safety and continuous input.