QA Technician II: Medical Devices & Growth

Hamilton Medical, Inc.; Reno (NV); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Paid vacation

Disability insurance

401(k)

Tuition reimbursement

Job summary

Hamilton Medical, Inc. is seeking a Quality Assurance Technician II to support the production of medical equipment on the day shift: 7:00am – 3:30pm. You will collaborate with quality and manufacturing teams to perform inspections of precision parts and clearly document results.

The ideal candidate has at least 2 years of QA experience and knowledge of GMP, FDA QSR 820, and ISO standards, plus an electronics background. Benefits and growth opportunities accompany this role.

Qualifications

• High school diploma or GED required; electronics degree preferred.
• At least 2 years of QA experience in medical devices or regulated industry QA/QC.
• Knowledge of GMP and FDA QSR 21 CFR Part 820; ISO 13485:2016 or ISO 9001.
• Strong technical, documentation, and communication skills.
• Ability to follow written instructions and take initiative.
• Experience with inspection techniques and measurement tools is a plus.

Responsibilities

• Perform dimensional and visual inspections of precision parts.
• Use appropriate measurement tools and document inspection results.
• Generate and maintain inspection documents, noting discrepancies.
• Assist engineers in identifying and troubleshooting discrepant materials.
• Assist QA team in creating policies and procedures.
• Other duties as assigned.

Skills

GMP knowledge

Quality assurance methods

Documentation skills

Communication skills

Initiative

Teamwork

Education

High School Diploma or GED

Associate degree in Electronics or Biomedical Electronics Technology

Job description

Hamilton Medical, Inc. is seeking a Quality Assurance Technician II to support the production of medical equipment on the day shift: 7:00am – 3:30pm. You will collaborate with quality and manufacturing teams to perform inspections of precision parts and clearly document results.

The ideal candidate has at least 2 years of QA experience and knowledge of GMP, FDA QSR 820, and ISO standards, plus an electronics background. Benefits and growth opportunities accompany this role.