Quality Technician

Meet Life Sciences; Acton (MA); On-site; USD 65,000 - 90,000; Full time

Job summary

Meet Life Sciences in Acton, MA is seeking a Post Market Quality Technician to support product investigations, testing, and quality system activities for FDA-approved medical devices.

You will perform product testing and failure analysis, conduct post-market investigations, maintain quality records including CAPAs and NCRs, review quality documentation, analyze quality data, and assist during FDA and ISO audits.

Qualifications

• Associate's Degree in Engineering, Science, or a related field.
• Electrical and/or mechanical troubleshooting experience preferred.
• Experience in a regulated environment (medical device preferred).
• Knowledge of QSR and/or ISO 13485.
• Strong documentation and Microsoft Excel skills.

Responsibilities

• Perform product testing and failure analysis
• Conduct post-market investigations
• Maintain quality records including CAPAs and NCRs
• Review quality documentation and records
• Analyze and trend quality data
• Support FDA and ISO audits

Skills

Documentation

Microsoft Excel

Troubleshooting

Regulated environment experience

QSR/ISO13485 knowledge

Education

Associate's Degree in Engineering/Science or related field

Job description

I'm partnering with a leading medical device company seeking a Post Market Quality Technician to support product investigations, testing, and quality system activities for FDA-approved medical devices.

Requirements

• Associate's Degree in Engineering, Science, or a related field
• Electrical and/or mechanical troubleshooting experience preferred
• Experience in a regulated environment (medical device preferred)
• Knowledge of QSR and/or ISO 13485
• Strong documentation and Microsoft Excel skills

Responsibilities

• Perform product testing and failure analysis
• Conduct post-market investigations
• Maintain quality records including CAPAs and NCRs
• Review quality documentation and records
• Analyze and trend quality data
• Support FDA and ISO audits

Preferred

• 2+ years of Quality experience
• Medical device industry experience