Medical Devices jobs

The Business Development Manager will be responsible for driving growth and expanding the company's market share in the medical connectors sector. This role requires a strategic thinker with a strong background in medical devices and connectors, as well as exceptional sales and relationship-building skills.

The NPI Engineer is responsible for transitioning new medical device projects from early development into controlled manufacturing, focusing on process development, assembly design, and documentation. This role involves collaborating with cross-functional teams, optimizing processes, and mentoring junior engineers while ensuring compliance with industry standards.

The Field Application Engineer is based remotely in Silicon Valley and will develop motion control applications across the laboratory automation and medical device industries. This person will work alongside customer and internal engineering teams to create new product specifications including centrifuge control, microscope control, and robotic controls.

This Manufacturing Engineer will have the opportunity to join a medical device manufacturer supplier based out of an 200,000 sq. ft. facility North West of Chicago. This individual should have a background in Plastic Injection Molding ,R&D, and New Product Integration

Are you an EHS Manager or Director with 10+ years of experience in the Life Sciences, Medical Device, Food Manufacturing, or Aerospace & Defense industry? Do you have thorough knowledge of OSHA 29 CFR Part 1910 and 1926? If so, please read on and apply to the EHS Director - Pharmaceutical Manufacturing opening based near Providence, RI. Relocation is available.

Our client is a precision machining company serving the Aerospace, Medical Device, and Hydraulic Industries, with over 70 years of experience and a strong reputation in the aerospace sector. They operate a state-of-the-art facility equipped with advanced technology, focusing on high-quality components that meet strict industry standards. Committed to sustainability and innovation, the company aims to enhance performance and reliability in aviation.

This company is seeking a Software Quality Design Engineer to oversee quality engineering tasks for pharmaceutical manufacturing, including risk management, documentation, and CAPA management. The ideal candidate will have 2-5 years of experience in medical device software quality, expertise in risk management (ISO 14971, FMEA), and a background in Agile methodologies. This is a fully onsite position in Middlesex County, MA.