Medical Device Quality Writer & Project Lead

Infotree Global Solutions; North Haven (CT); On-site; USD 70,000 - 90,000; Full time

Job summary

A medical technology company is seeking a Quality Engineer II to support risk assessments, design change quality reviews, and address quality issues throughout the medical device lifecycle. The ideal candidate will possess a Bachelor's or Master's degree and relevant experience, demonstrating skills in technical writing, data analysis, and project management. This position requires collaboration across engineering, manufacturing, and quality assurance functions to maintain high standards and improve processes.

Qualifications

• Minimum of 2 years of relevant experience or 0 years with advanced degree.
• Practical knowledge within the job area obtained through education and experience.

Responsibilities

• Develop, modify, and maintain quality standards and protocol for products.
• Collaborate with engineering to ensure quality standards.
• Conduct quality assurance tests and perform statistical analysis.

Skills

Technical writing

Data analysis

Project management

Education

Baccalaureate degree or Master's degree

Job description

A medical technology company is seeking a Quality Engineer II to support risk assessments, design change quality reviews, and address quality issues throughout the medical device lifecycle. The ideal candidate will possess a Bachelor's or Master's degree and relevant experience, demonstrating skills in technical writing, data analysis, and project management. This position requires collaboration across engineering, manufacturing, and quality assurance functions to maintain high standards and improve processes.