Quality Technician - Medical Device Quality & Compliance

Nextern

Maple Grove (MN)

On-site

USD 55,000 - 75,000

Full time

14 days+

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Benefits offered by this job

Health Care Plan (Medical, Dental &amp
Retirement Plan with Company Match
Paid Time Off, Personal Days, AND
Birthday Holiday!
Lifetime Membership Subsidy and Welll
Life Insurance (Basic, Voluntary &
MN Paid Leave
Short-Term & Long-Term Disability
Taco Thursdays!!!

Job summary

Nextern Maple Grove is seeking a QA/Manufacturing Technician to ensure production and process control compliance during the development and manufacturing of medical devices at our Maple Grove facility. This role emphasizes hands-on monitoring of production staff and adherence to documented quality standards.

Responsibilities include performing comprehensive DHR reviews at close of manufacturing and product release, determining disposition with operators, writing technical reports, and providing

Qualifications

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

Responsibilities

  • Monitor and train production staff for process control.
  • Perform comprehensive Manufacturing Device History Record (DHR) review at close of manufacturing and product release.
  • Make decisions on handling product issues with operators and release determinations.
  • Provide technical support to the Quality group and write technical reports and quality documentation.
  • Maintain safe, clean, and organized work area; participate in continual improvement.

Skills

Quality control
Communication skills
Reading engineering drawings
Excel/Office tools

Tools

Excel
Word
Outlook
ERP/PLM

Job description

Nextern Maple Grove is seeking a QA/Manufacturing Technician to ensure production and process control compliance during the development and manufacturing of medical devices at our Maple Grove facility. This role emphasizes hands-on monitoring of production staff and adherence to documented quality standards.

Responsibilities include performing comprehensive DHR reviews at close of manufacturing and product release, determining disposition with operators, writing technical reports, and providing

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