Medical Devices jobs

Our client is a medical device manufacturer located in the Northern Suburbs of Milwaukee. With over 5 locations throughout the US and 5000 employees, they have continued to grow out new product lines. They seek a Quality Engineer to join their Quality team and oversee 3 production lines.

The Production Manager will manage and optimize the use of equipment, materials, and labor to achieve production goals. The Production Manager will also coordinate maintenance and repair activities to minimize downtime and ensure equipment reliability.

The Principal Engineer will play a pivotal role at my client's rapidly growing operation, serving as a technical lead and subject matter expert on plastic molding processes. You will drive the manufacturing process from product concept up to final production. Join a phenomenal company renowned for their culture and offerings for their employees, and take the next step in your career!

A medical device manufacturer based in the Western Suburbs of Chicago is looking to add a Quality Assurance Engineer to their growing team. The ideal candidate will have experience in a similar manufacturing environment. This fast-expanding company is making waves in the medical device industry with its highly innovative product line.

A medical device manufacturer based in the Western Suburbs of Chicago is looking to add a Quality Assurance Engineer to their growing team. The ideal candidate will have experience in a similar manufacturing environment. This fast-expanding company is making waves in the medical device industry with its highly innovative product line.

The Manufacturing Engineer will sit on a small team reporting into the Manufacturing Engineering Manager. In this role you will get to work autonomously, wearing many hats, supporting the manufacturing of surgical medical devices.

The Facilities Maintenance Manager will be responsible for managing all aspects of the company's facilities and maintenance department. This includes maintaining and repairing machinery, equipment, and other items to ensure proper functionality and cost-efficiency. Key duties involve repairs, preventive maintenance on molding machines and facilities, and troubleshooting electrical, hydraulic, and control systems.

The CNC Process Engineer is responsible for recommending process improvements to maximize machine capabilities and efficiency. The CNC Process Engineer will also support troubleshooting, provide technical expertise, and design, program, and optimize CNC machining processes for both new product development and existing projects.

An opportunity to report into to Director of Ops to generate manufacturing documentation for new products as well as develop process improvements. The job entails support manufacturing, documentation and quality personnel in ISO 13485, GMP controlled environment to a fast growing organization with great room to grow into new opportunities.

The Quality Manager will be responsible for overseeing the quality assurance and control processes with my client and report into the General Manager of the site. This role involves developing, implementing, and maintaining quality management systems to ensure compliance with industry standards and customer requirements.

In this Manufacturing Engineer role you will play a key role in the development, implementation, and optimization of manufacturing processes for medical device while positively affecting quality, delivery, cost and safety. This position requires a strong background in manufacturing engineering, problem-solving skills, and the ability to manage multiple projects simultaneously.

The Manufacturing Engineer will develop and implement efficient manufacturing processes and methods while coordinating the launch of new or revised products in a medical device environment. The role involves designing production processes, troubleshooting mechanical issues, and training production personnel to ensure quality and compliance with specifications.

As a Manufacturing Engineer, you'll create and implement efficient, cost-effective manufacturing processes that meet product specifications and quality standards. You'll also suggest improvements to our production methods and controls, and play a key role in launching new or updated products.

As the Manufacturing Engineer at the medical device company, you will discover new ways of implementing cost-effective processes. You will troubleshoot and make improvements to manufacturing processes and collaborate with teams on product launches.

Our client is a medical device manufacturer located in the Western Suburbs of Chicago. They seek a Quality Assurance Engineer to join their expanding team with a background in a similar manufacturing setting. This organizaiton is growing rapidly with an extremely innovative product line that's taking the Medical Device world by storm.

The NPI Engineer will be vital in designing and developing new medical devices. Key responsibilities include creating assembly and test fixtures, assisting with validation studies, and optimizing processes. The engineer will ensure compliance with industry standards, contribute to manufacturing instructions, and provide training on assembly processes. The role also involves collaborating with cross-functional teams, troubleshooting complex issues, and understanding materials science relevant to medical devices.

Our client is a medical device manufacturer located in the Western Suburbs of Chicago. They seek a Quality Assurance Engineer to join their expanding team with a background in a similar manufacturing setting. This organizaiton is growing rapidly with an extremely innovative product line that's taking the Medical Device world by storm.

A medical device manufacturer based in the Western Suburbs of Chicago is looking to add a Quality Assurance Engineer to their growing team. The ideal candidate will have experience in a similar manufacturing environment. This fast-expanding company is making waves in the medical device industry with its highly innovative product line.

The NPI Engineer will be a key player in the development of essential medical device products through design development into manufacturing through the entire product life cycle phase.

Our client is seeking a skilled New Product Introduction Engineer to join our team. The ideal candidate will have a strong background in NPI engineering within the medical device industry, particularly in the realm of injected molded components. This role involves prototyping, process development, and rigorous testing to deliver safe and effective products for the healthcare market.

Our client is seeking a skilled New Product Introduction Engineer to join our team. The ideal candidate will have a strong background in NPI engineering within the medical device industry, particularly in the realm of injected molded components. This role involves prototyping, process development, and rigorous testing to deliver safe and effective products for the healthcare market.

The Senior Software Quality Engineer is responsible for ensuring product quality during the software development life cycle, involving design, verification, and validation processes. Candidates should have at least eight years of experience in quality engineering within regulated industries, with knowledge of ISO standards and the ability to conduct risk management and internal audits.

The Design Quality Engineer in Medical Device Manufacturing will lead quality system and design assurance activities for New Product Development (NPI), ensuring compliance with FDA 21 CFR Part 820, ISO 13485, and EU Medical Device Regulations. They will play a key role in maintaining quality standards for Class III medical devices throughout the product lifecycle at our Westborough, MA facility.

The Design Quality Engineer is responsible for leading quality system and design assurance efforts during New Product Development (NPI) to ensure compliance with FDA 21 CFR Part 820, ISO 13485, and EU Medical Device Regulations for Class III medical devices. This role involves managing design controls, risk management, documentation, and regulatory compliance throughout the product lifecycle.

This role focuses on supporting product development and manufacturing processes to ensure compliance with medical device quality standards. Key responsibilities include working with cross-functional teams to maintain compliance with FDA and ISO regulations, overseeing design controls, risk management, and verification/validation activities, and ensuring that product designs meet stringent quality and safety standards.

This role involves implementing and maintaining quality systems aligned with regulatory requirements, ensuring compliance with ISO 9001 and GMP standards. Responsibilities include developing team capabilities, overseeing audits, driving process improvements, and maintaining regulatory compliance across the organization.

The Senior Quality Manager ensures compliance with regulatory requirements, ISO standards, and GMP for all products designed, manufactured, and distributed at the Norwood site. They lead strategic enhancements to the Quality Management System, oversee audits and inspections, and act as the site's Quality Management Representative.

The Senior Quality Manager, medical device manufacturing, will lead and manage the Quality Assurance and Control teams, overseeing the implementation and continuous improvement of the site's Quality Management System. They will work cross-functionally to ensure compliance with regulatory requirements, drive process improvements, and support new product development initiatives at our Westwood, MA location.

The Quality Manufacturing Engineer will oversee product quality assurance, including internal audits, customer complaint resolution, and process quality management, with a focus on precision injection molding. They will also lead quality training, support design reviews, and maintain quality documentation while ensuring compliance with ISO/QS standards at the Royalton, VT location.

The Senior Optical Engineer will be the lead engineer and manage a team of 3 on the optical manufacturing team.