Senior Design Assurance Engineer - Saint Paul

This role has a wide scope of responsibilities ranging from ensuring supplier design assurance, · supplier product development integration assurance, · and third-party manufacturing assurance.Apply strong engineering fundamentals to analyze supplied designs, · assess supplier pro ...

What You'll Do:    · The Design Assurance Engineer is part of the product design and development team and ensures quality and regulatory compliance throughout the medical device lifecycle for class I and II reusable surgical instruments and disposable medical devices and supports ...

The Design Assurance Engineer is part of the product design and development team and ensures quality and regulatory compliance throughout the medical device lifecycle for class I and II reusable surgical instruments and disposable medical devices. · ...

A Senior Quality Assurance Engineer ensures the quality, reliability and security of enterprise applications and services in a rapidly evolving digital landscape. · ...

· Additional Location(s):  N/A · Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance · At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackl ...

· Additional Location(s):  N/A · Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance · At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackl ...

Scanlan International, Inc., is a medical device company specializing in surgical instruments. · This Design Assurance Engineer will lead product quality assurance for new product development projects. · ...

The Design Assurance Engineer provides critical quality and regulatory oversight to ensure that all design and development activities for medical devices comply with internal quality requirements and external regulatory standards. · ...

A growing medical device company in the Twin Cities is hiring a Senior Design Assurance Engineer to lead quality and compliance efforts throughout product development. This individual will partner closely with engineering to ensure design activities align with FDA and ISO require ...

We are looking for an experienced QA Engineer with strong expertise in C#, Selenium automation, and deep exposure to healthcare standards and imaging systems.The ideal candidate will have hands-on experience in Medicare/Medicaid (Medicate) domain, along with solid knowledge of HL ...

An established Medical Device company is seeking an experienced Design Quality Engineer. · ...

The Quality Assurance Engineer assists efforts associated with ensuring products released to customers error-free and with expected or better performance. This includes providing input on the design, and direct engagement in the development and implementation of an automated test ...

Seeking a Quality Assurance professional to support quality systems and compliance activities in a regulated medical device environment. · Support QMS activities in compliance with FDA 21 CFR 820 and ISO 13485. · ...

As a Design Assurance Engineer you will play a pivotal role in supporting the development and assurance of new products. · ...

As a Design Assurance Engineer, · You will play a pivotal role in supporting the development and assurance of new products. · ...

Support the development and assurance of new products. · Participate in New Product Development Phase Reviews. · Collaborate with R&D to define and manage design inputs and outputs. · ...

As a Design Assurance Engineer, you will play a pivotal role in supporting the development and assurance of new products. · ...

As a Design Assurance Engineer at Actalent you will play a pivotal role in supporting the development and assurance of new products. You will engage in phase reviews and design reviews collaborating closely with R&D to manage design inputs and outputs ensuring adherence to design ...

We are seeking a Quality Assurance professional to support quality systems and compliance activities in a regulated medical device environment. · Support QMS activities in compliance with FDA 21 CFR 820 and ISO 13485. · Review and approve quality documents (SOPs, CAPA, deviations ...

+ Participate in New Product Development Phase Reviews and lead or participate in Design Reviews. · + Collaborate with R&D to define and manage design inputs and outputs.Essential Skills · Degree in Engineering, preferably Electrical or Software Engineering. · Minimum of 2 years ...