What are the responsibilities and job description for the Quality Engineering Technician position at JMD Technologies Inc.?
Title: Senior Quality Engineering Technician
Location: Hartford, NY (100% Onsite)
Employment Type: Contract (6 Months)
Status: Accepting Candidates
About the Role
Join a medical device manufacturing organization supporting advanced Nitinol manufacturing operations. This role provides customer-facing and factory-facing quality support while driving quality systems execution, validation activities, inspection support, and continuous improvement initiatives.
The ideal candidate will have experience working within regulated manufacturing environments supporting quality systems, investigations, validations, and inspection activities.
Key Responsibilities
- Quality Systems Support
- Own and drive timely processing of:
- Nonconformances
- Process Deviations
- Quality Records
- Support compliance with:
- ISO 9001
- ISO 13485
- FDA 21 CFR Part 820
- Support CAPA execution and effectiveness activities
- Validation & Quality Engineering Support
- Support process validation activities
- Execute validation protocols and data collection activities
- Perform validation data analysis
- Support:
- Gage R&R studies
- Test Method Validations
- Assist with preventive action execution activities
- Inspection & Testing Support
- Perform and oversee:
- Sample preparation
- Product testing
- Material inspections
- Support testing activities including:
- Tensile Testing
- BFR Testing
- DSC Testing
- Chemical Testing
- Lead disposition recommendations for:
- Bar
- Coil
- Wire
- Thick Sheet materials
- Continuous Improvement
- Maintain calibration programs
- Maintain:
- Control Plans
- Process FMEAs (pFMEAs)
- Support continuous improvement initiatives
- Support customer and manufacturing quality activities
Qualifications
- High School Diploma or equivalent required
- Minimum 3 years of quality experience
- Examples:
- Quality Technician
- Quality Inspector
- Quality Analyst
- Quality Engineering Technician
- Experience supporting quality systems within regulated manufacturing environments
- Experience with:
- Nonconformances
- Deviations
- CAPAs
- Quality Documentation
- Strong technical writing skills
- Strong communication skills
- Ability to independently manage technical assignments
Preferred Qualifications
- Medical Device manufacturing experience
- ISO 13485 experience
- FDA regulated manufacturing experience
- Calibration program experience
- Process Validation experience
- Gage R&R experience
- Test Method Validation experience
- Experience with Nitinol manufacturing processes
- pFMEA and Control Plan experience
Compensation
- $36/hr W2
- Contract Duration: 6 Months
- Location: Hartford, NY
Salary : $36