Quality Engineer: Technical Writing & Process Improvement

IntePros; North Haven (CT); Hybrid; USD 85,000 - 110,000; Full time

Job summary

IntePros seeks a Quality Engineer – Technical Writing to drive technical documentation and risk-based quality improvements. Hybrid work arrangement allows 4 days onsite and 1 day remote, located in Connecticut, United States.

The role emphasizes DFMEAs, design change QA, and cross-functional collaboration to resolve quality issues while ensuring compliance with medical device standards.

Qualifications

• Bachelor’s degree with 2+ years of relevant experience or Master’s degree with minimal experience required.
• Medical device industry experience is required.
• Experience with design controls and DFMEAs is preferred.

Responsibilities

• Support risk assessments and quality reviews for design changes and product quality issues.
• Conduct product quality assessments and root cause investigations.
• Review risk management files and engineering change documentation.
• Develop technical documentation, including DFMEAs and related records.
• Analyze data and support quality/process improvement projects.
• Collaborate with Engineering, Manufacturing, and other teams.
• Ensure compliance with medical device quality standards and requirements.

Skills

Technical Writing

Data Analysis

Project Management

Education

Bachelor’s degree + 2 years relevant experience

Master’s degree + 0 years relevant experience

Job description

IntePros seeks a Quality Engineer – Technical Writing to drive technical documentation and risk-based quality improvements. Hybrid work arrangement allows 4 days onsite and 1 day remote, located in Connecticut, United States.

The role emphasizes DFMEAs, design change QA, and cross-functional collaboration to resolve quality issues while ensuring compliance with medical device standards.