Engineering Manufacturing jobs in Engineering & Manufacturing

Our client is ranked among the top medical device companies that provide outsourced design and manufacturing solutions for surgical devices and scientific applications. They are now looking to hire a Manufacturing Engineering Technician to join their team in RI.

The Medical Device Manufacturing Engineer will function as a liaison with project engineering, manufacturing and the customer regarding the implementation of programs. The Medical Device Manufacturing Engineer will provide technical support/solutions to new manufacturing processes, manages to establish yield and throughput, and drives continuous improvement through production ramp up.

The Senior Quality Engineer will be responsioble for assisting in leading the quality team. Must be systems focused and a team player.

The Product Development Engineer will be customer centric, able to work on various ongoing projects at once, and can implement manufacturing processes. This role will have aspects of project management and manufacturing process improvement.

This position will be responsible for leading quality engineering activities associated with new product development, manufacturing, quality systems and risk management on devices. This is an individual contributor role which reports up to the Director of Quality Engineering and allows opportunity to build out the team.

The Automation & Controls Engineer will be responsible for the development and design of machine control systems.

The Mechanical Engineer would be responsible for product development and improvement initiatives, from component and assembly redesign, through the manufacturing floor in the regulated field of medical devices.

The Quality Manager will improve quality of products to delight consumers, serve customers and satisfy regulators, establish systems to assure quality and sustain quality improvements to deliver target quality, and build required competencies in the Quality organization to deliver global quality goals.

Our client is seeking an Engineering Project Manager to join their team in Providence, RI. As part of a succession plan, this position will be an individual contributor to start and will later have the opportunity to grow into engineering management. The main responsibilities of this role will include project management and equipment validation.

Serving in a lead role, the Senior Manager, Regulatory Affairs -Medical Device will lead regulatory affairs submissions for product development globally. As the company sells products in new countries/regions and there are regulatory issues to navigate across the globe such as MDR requirements in Europe- which will be led by this person.

This position requires ongoing interface with engineering, manufacturing, suppliers and customers. Responsibilities include:

Support and implement quality systems requirements in design, supply chain management, manufacturing, assembly & test, and customer support for all product lines.

Design and implement product improvement, cost reduction, new product development and product issue resolution efforts for Mortise Lock Engineering. Part of a creative team in developing mechanical and electromechanical systems, fixing problems or creating solutions to customer needs. Maintain engineering documentation relative to a product and administer changes to the documentation. Develop detailed knowledge of the Mortise Lock product lines.

Immediate hire looking for Supplier Quality Engineer for a fast-paced, well-known Medical Devices Manufacturing company in the Greater Boston area. Competitive compensation for a candidate with experience with quality systems, external supplier audits, and medical device FDA regulations.

The Senior Process/Quality Engineer position is a key need for this client as this person will work directly with multiple departments at their North American Headquarters. The ideal candidate will come from a blended background within process & quality engineering and have experience with APQP, PPAP, etc.