Quality Engineering Technician

LS Solutions; Point Pleasant (NJ); On-site; USD 75,000 - 110,000; Full time

Job summary

LS Solutions in New Jersey is seeking a quality-focused professional to support engineers in a medical device manufacturing setting. You will participate in investigations, calibration, documentation, corrective actions, and continuous improvement activities.

Responsibilities include executing validation protocols (Gage R&R), aiding CMM programming, applying GMP/GDP requirements, interpreting drawings with GD&T, and maintaining accurate quality records to drive root-cause analysis and

Qualifications

• Strong understanding of quality systems and medical device compliance (GMP/GDP).
• Proficiency in validation, measurement systems analysis (Gage R&R), and statistical data analysis.
• Working knowledge of CMM programming and SPC documentation.
• Ability to interpret engineering drawings and apply GD&T.
• Attention to detail, documentation accuracy, and continuous improvement mindset.

Responsibilities

• Execute validation protocols, including Gage R&R testing and data analysis.
• Assist with CMM programming and development of SPC templates.
• Apply GMP and GDP requirements to ensure compliant quality processes.
• Interpret blueprints and apply GD&T knowledge to support measurement and verification activities.
• Maintain accurate quality documentation and support root-cause problem solving.

Skills

Quality systems

GMP/GDP

Validation & Gage R&R

GD&T interpretation

Attention to detail

Tools

CMM programming

SPC documentation

Job description

Provide support to quality engineers in a medical device manufacturing setting by performing investigations, calibration, documentation, corrective actions, and continuous improvement activities.

Key duties

• Execute validation protocols, including Gage R&R testing and data analysis.
• Assist with CMM programming and development of SPC templates.
• Apply GMP and GDP requirements to ensure compliant quality processes.
• Interpret blueprints and apply GD&T knowledge to support measurement and verification activities.
• Maintain accurate quality documentation and support root-cause problem solving.

Qualifications / Skills

• Strong understanding of quality systems and medical device compliance (GMP/GDP).
• Proficiency in validation, measurement systems analysis (Gage R&R), and statistical data analysis.
• Working knowledge of CMM programming and SPC documentation.
• Ability to interpret engineering drawings and apply GD&T.
• Attention to detail, documentation accuracy, and continuous improvement mindset.