• The Quality Engineer helps oversee all Quality functions at the plant level.
• This Engineer will work cross-functionally to collaborate with internal and external customers

• Conduct Supplier Quality Engineering functions and provide utilization of Six Sigma Green Belt
• Communicate and understand fuel cell stack and electromechanical needs to management and staff

Our client is seeking a Manufacturing Quality Engineer to grow their relaxed, team-based work environment. They are seeking an individual with strong experience in a manufacturing environment preferably in a regulated industry.

Identify and implement quality improvements throughout product development to ensure all customer standards are met.

Work directly with internal and external customers to identify any nonconformances and implement appropriate corrective and preventative actions.

Manage plant's compliance of ISO and EHS standards.

Train facility employees on EHS programs and make suggestions for any improvements.

Our rapidly growing medical device client (OEM), is looking to hire a Senior Manufacturing Engineer to join their team in assisting sustaining engineering activities associated with the production of their innovative & transformative/life changing organ transplant devices.

As the Quality Manager, you will be responsible for performing tasks designed to uphold and improve product quality, while also simultaneously meeting regulatory standards to stay in compliance. You would be working with complex cardiovascular medical devices in a high visbility role.

Develop, implement, and maintain manufacturing processes of medical devices.

Lead initiatives to reduce manufacturing costs and improve product yields.

• The Quality Manager oversees all Quality functions at the plant level.
• This Manager will work cross-functionally to collaborate with internal and external customers

Our rapidly growing medical device client (OEM), is looking to hire a Senior Manufacturing Engineer to join their team in assisting sustaining engineering activities associated with the production of their innovative & transformative/life changing organ transplant devices.

The Senior Manufacturing Engineer in this role will be responsible for improving productivity and yield, leading in root cause analyses, updating SOPs and writing and participating in engineering trials.

Join our client which has 28+ products in their portfolio and are commercialized in 90+ countries.

Reporting to the Director of Quality, the Quality Manager, will perform tasks that will uphold and improve the product quality of the medical devices manufactured and meet regulatory requirements to stay in compliance for the Burlington Manufacturing site.

Producing a patented, nonstick coating for surgical devices across the nation, our client has been a trusted supplier to top medical device manufacturers in the United States for generations. The Quality Engineer will be the focal point of the Quality team as the Director moves into an overseeing role.

The Senior Manufacturing Engineer in this role will be responsible for improving productivity and yield, leading in root cause analyses, updating SOPs and writing and participating in engineering trials.

Implement product design control activities for product development initiatives, both new and existing.

Review and maintain all documentation with regards to technical design.

Provide Quality Engineering support for NPD, Manufacturing, and other Supply Chain functions throughout all phases of Design Controls. This is a collaborative position working closely with R&D, Manufacturing, Sales & Marketing, and others to ensure a constant state of control and compliance with QMS, and FDA QSR requirements.

he NPI Engineering II is primarily responsible for utilizing state of the art equipment for the development of life changing medical devices. The ideal candidate will be comfortable operating a variety of equipment including, but not limited to; spin developers, sputtering machines, lasers, injection molders, reflow machines as well as an array of test equipment while adhering to the quality requirements of the company.

Our rapidly growing medical device client (OEM), is looking to hire a Senior Manufacturing Engineer to join their team in assisting sustaining engineering activities associated with the production of their innovative & transformative/life changing organ transplant devices.

In this role you will have the opportunity to work with a company dedicated to eliminating CO2 emissions from industrial engineering processes. My client is seeking someone with engineering know how, PLC experience, and a desire to contribute to solving the climate change problem.

Internationally recognized organization, focusing on the design and manufacture of high-reliability Connectivity, Power & Control solutions for the Aerospace, Defense and Space industries, is seeking a Sr. Electrical Engineer to lead fundamental electrical architectures and designs that define both new products and product improvements.

You will be responsible for systems engineering support of technical projects. You will be conducting analysis, investigations, and testing in product development and production issues.

Maintain and develop a lively Environmental, Health and Safety training program which ensure all safety procedures and processes are followed. Conduct frequent audits, make sure all personnel are trained and dedicate yourself to fostering a culture that places safety as the top priority.

• The Supply Chain Quality Manager will manage product and process quality across the supply chain.
• This manager will support implementing data collection means and reporting methods related to chemistry related processes and environments

The Product Life Cycle Engineer in this role will serve as the hands on Engineer responsible for development or revision of testing protocols and reports aimed at continued regulatory compliance with existing and revised industry standards related to Class I, II and III medical devices.

The Sr. Supplier Engineer will work closely with peers in Quality, Sourcing, and Life-cycle Engineering to lead and implement new capital equipment and tooling at suppliers, carry out new product introductions, execute improvement projects, resolve business-critical technical issues, and investigate and lead corrective actions in response to quality issues across the supply base.

The Senior Applications Engineer in this role will be responsible for leading project teams in the development of new processes and commercialize programs as necessary. The engineer in this role will also be responsible for meeting with internal employees and customers to help them understand product requirements, features and benefits.

Run daily Quality activities focusing on eQMS and new product development as they release a new line of applicators' for easy application. This combination device manufacturer focuses on wound-healing devices from a tissue front.

Provide Quality Engineering support for NPD, Manufacturing, and other Supply Chain functions throughout all phases of Design Controls. This is a collaborative position working closely with R&D, Manufacturing, Sales & Marketing, and others to ensure a constant state of control and compliance with QMS, and FDA QSR requirements.

The Senior Regulatory Affairs Specialist will facilitate EU/MDR and FDA regulations for a class III complex OEM as they alter and release life saving products throughout various markets.

The Mechanical Engineer will work in a small team to develop, design, and test large and complex secondary packaging machines. The incumbent will visit customers remotely and traveling to customer facilities to diagnose issues in the field.