Quality Engineer jobs

The Quality Engineer (Medical Device) will lead quality initiatives in a highly regulated, precision manufacturing environment, ensuring compliance with ISO 13485 and FDA 21 CFR Part 820 while driving continuous improvement across processes and systems. This position offers a clear path to advancement, and offers outstanding development opportunites.

The Senior Quality Engineer is responsible for leading quality assurance efforts across the product life cycle, from development to post-launch, ensuring high reliability and customer satisfaction. It involves cross-functional collaboration, testing oversight, and continuous improvement of quality systems and processes.

The Senior Quality Engineer will develop and implement quality assurance plans, conduct rigorous testing, and lead cross-functional teams to ensure the reliability, safety, and performance of connected fitness products.

Take on a pivotal role as a Quality Engineer in Hartford, CT, ensuring in-process and final quality compliance for precision-manufactured components in aerospace and medical industries. Utilize your expertise in AS9100, ISO9001, and lean manufacturing to lead quality improvements, collaborate with diverse teams, and implement advanced inspection technologies in a dynamic and impactful environment.

The Senior Quality Engineer will lead Quality Assurance processes, mentor Quality Engineers, and act as the voice of the customer to ensure that quality expectations are consistently met. They will analyze and standardize quality procedures while training employees in quality and continuous improvement methodologies at our Belmont, NH facility.

Our client is hiring a Senior Quality Engineer to join our experienced team, reporting directly to the Quality Manager. This position plays a key role in driving core quality tools, contributing to ongoing continuous improvement initiatives, and providing essential support to production operations at the facility.

The Quality Engineer (medical device manufacturing) plays a key role in ensuring product and process quality through all phases of development, validation, and production, in compliance with ISO 13485 and FDA regulations. This individual will lead root cause investigations, support design controls, and drive continuous improvement initiatives in a fast-paced, innovation-focused environment.

As the Quality Engineer you will gain hands on experience in medical device development, focusing on manual testing, design controls, sterilization, and transit testing. You will collaborate closely with mechanical engineers and cross functional teams to ensure compliance with FDA regulations and ISO 13485 standards.

Our client, a fast-growing and forward-thinking automotive parts manufacturer, is making significant investments in advanced technology and skilled professionals to fuel their growth. A key priority is enhancing their quality engineering department. They are currently looking to add two seasoned Quality Engineers to their premier facility.

My client, a global outdoor products manufacturer is seeking a Supplier Quality Engineer in the Oxford, CT area to lead supplier quality initiatives, ensure compliance with ISO/IATF standards, and drive performance improvement across development projects. This role focuses on supplier audits, PPAP ownership, and quality systems implementation to support high-performance product delivery.

The Sr. Quality Engineer will report to Quality Manager and assist with all needed actions to maintain the quality system at the site here in the Southwest Chicago Suburbs. This person should be a strong leader that can make decision quickly and has the foundational skills needed to succeed as a Quality Engineer.

Are you a Quality Engineer who has experience with Calypso CMM Programming and looking for your next opportunity? Do you want to join a company that is looking to double in size over the next 3 years? Do you have a strong understanding of CNC Machining & CMM Programming? If so, please read on and apply to the Quality Engineer opening in Chittenango, NY.

Our client is seeking a Senior Quality Engineer to manage their lab operations and lead key quality processes on a daily basis. This position offers the opportunity to enhance your quality engineering expertise while taking on a leadership role with junior engineers.

A leading global automotive manufacturer is seeking a Senior Quality Engineer to join their quality team in a leadership capacity. This role includes managing customer relations and complaints, overseeing PPAP documentation, and taking the lead on FMEA and Control Plan development.

The Quality Engineer Manufacturing will lead root cause investigations, support continuous improvement initiatives, and ensure compliance with internal and external quality standards. They will collaborate cross-functionally to improve processes, enhance product quality, and maintain robust documentation within the Quality Management System.

This Quality Engineer will be responsible for ensuring unwavering compliance with stringent standards including AS9100, AS13100, and NADCAP. They will actively supporting product and process quality engineering initiatives and be a critical contributor to maintaining and enhancing our quality systems,They will focus in driving continuous improvement efforts, and guaranteeing regulatory compliance throughout our Nuclear/Aerospace manufacturing processes.

Our client, an innovative and rapidly growing automotive parts manufacturer, is heavily investing in new technology and top talent to support their expansion. A major focus of this investment is strengthening their quality engineering team. They are currently seeking two experienced Quality Engineers to join their flagship facility.

The Quality Engineer, medical device manufacturing, will work to improve the quality of products and processes while operating in a culture highly receptive to quality. You will have the opportunity to support and provide guidance to ensure adherence to processes and procedures that maintain safety, efficacy, and compliance with applicable standards and regulations onsite at out Hudson, NH facility.

This is a distinctive opportunity to step into a senior-level role focused on Quality and Process Improvement. The position is responsible for managing quality assurance and process control for large-scale industrial systems and metal-welded frame assemblies

The Senior Quality Engineer will lead the execution and continuous improvement of the company's quality system, ensuring compliance with ISO9001, ISO13485, and IATF16949 standards. They will oversee quality planning, audits, root cause analysis, and supplier/customer interactions while supporting engineering teams through validation, PPAP, and process capability initiatives at the West Hartford, CT site.

This Quality Engineer role focuses on driving product quality improvements through data analysis, root cause investigations, and compliance with ISO 9001 and ISO 13485 standards. The position involves interfacing with customers, leading internal audits, and implementing advanced metrology and statistical tools to enhance production processes.

The Quality Engineer will lead quality initiatives in a highly regulated, precision manufacturing environment, ensuring compliance with ISO 13485 and FDA 21 CFR Part 820 while driving continuous improvement across processes and systems. This position offers a clear path to advancement, and offers outstanding development opportunites.

The Senior Quality Engineer will lead quality initiatives across new product introduction and sustaining efforts, collaborating with engineering, manufacturing, and support teams to ensure product reliability and customer satisfaction. They will drive root cause investigations, implement quality controls, and support continuous improvement throughout the product lifecycle at their downtown Boston, MA facility.

The Quality Engineer will support product quality through hands-on inspection, failure analysis, and root cause investigation across new product introductions, customer returns, and in-process manufacturing. They will also play a key role in maintaining ISO 9001 compliance, driving continuous improvement, and collaborating with engineering, manufacturing, and suppliers.

A leading global automotive manufacturer is seeking a Senior Quality Engineer to join their quality team in a leadership capacity. This role will be responsible for managing customer communications and resolving complaints, overseeing PPAP documentation, and leading the development and execution of FMEA and Control Plans.

This Product Development Quality Engineer role involves ensuring adherence to strict quality and regulatory standards throughout product and process lifecycles, leading quality initiatives, and driving continuous improvement. Responsibilities also include technical leadership, mentorship, and collaboration with internal and external stakeholders to guarantee the development of high-quality, compliant medical devices

The Senior Quality Engineer will lead Quality Assurance processes, mentor Quality Engineers, and act as the voice of the customer to ensure that quality expectations are consistently met. They will analyze and standardize quality procedures while training employees in quality and continuous improvement methodologies at our Belmont, NH facility.

The Design Quality Engineer is responsible for ensuring that medical device components meet customer and regulatory requirements through root cause analysis, corrective actions, and continuous improvement initiatives. The role involves close collaboration with engineering, production, and quality teams to support new product introductions and maintain consistent product quality.

Our client, a global automotive manufacturer, is looking for a Senior Quality Engineer to take on a leadership role within the quality department. The Senior Quality Engineer will be responsible for engaging with customers and addressing customer complaints, overseeing PPAP documentation, and leading FMEAs and Control Plans

The Quality Engineer (medical device manufacturing) plays a key role in ensuring product and process quality through all phases of development, validation, and production, in compliance with ISO 13485 and FDA regulations. This individual will lead root cause investigations, support design controls, and drive continuous improvement initiatives in a fast-paced, innovation-focused environment.