- Hologic (Marlborough, MA)
- …teams in the execution of design changes, product enhancements, and quality projects for medical device products. This position plays a vital role in ensuring ... our innovative team at **Hologic** as a **Senior Design Engineer , R&D ** , where you will lead...experience, with a preference for 3 years in a medical device process and/or product development environment.… more
- Capgemini (Burlington, MA)
- …verification strategies, manage a team of engineers, and ensure compliance with medical device regulations. **Your Role** . Lead Verification Strategy: Develop ... systems. . Compliance & Standards: Ensure all verification activities align with relevant medical device regulations such as ISO 13485, IEC 62304, and FDA… more
- Capgemini (Waltham, MA)
- …and motivated Qt/C Software Engineer to lead the development of standalone medical device applications on Linux. In this role, you'll collaborate with a ... modern Qt and C (11' or newer) based standalone medical device applications in Linux OS +...Relief **About Capgemini Engineering** World leader in engineering and R&D services, Capgemini Engineering combines its broad industry knowledge… more
- Hologic (Marlborough, MA)
- …Are you passionate about driving innovation while ensuring compliance and quality in medical device development? At Hologic, we are seeking a **Lead Design ... Lead Design Assurance Engineer Newark, DE, United States Marlborough, MA, United...to hear from you! **Knowledge:** + In-depth understanding of medical device regulations and standards, including ISO… more
- Capgemini (Boston, MA)
- …impact patient care and clinical outcomes. **Your role** + Design and develop standalone medical device applications using modern C on Linux OS. + Lead the ... job** **you're** **considering** Join Capgemini as aC /MATLAB Software Engineer and help shape the future of healthcare technology....in application software development, with 2 years in the medical device or other regulated industries. +… more
- Jabil (Clinton, MA)
- …partner companies and suppliers. This entry-level Test Engineer position will support medical device R&D staff within the Infusion Management Solutions ... (EDUCATION, EXPERIENCE, KEY REQUIREMENTS) - Bachelor's degree in Mechanical Engineering - Medical device internship experience preferred - Familiar with polymers… more
- Hologic (Marlborough, MA)
- …knowledge of FDA Quality System Regulations (especially Design Control), ISO 13485, EU Medical Device Regulation, ISO 14971, Risk Management, GMP, and GDP. + ... Senior Post Market Quality Engineer Newark, DE, United States Marlborough, MA, United..., you will lead quality engineering efforts for on-market medical devices. This role is responsible for evaluating post-market… more
- Olympus Corporation of the Americas (Westborough, MA)
- …matter expertise, technical guidance, and leadership for the application of health and medical device SW regulatory standards to the Olympus SDLC, including IEC ... + Minimum of 6 years of experience in a medical device setting. + Experience in the...teams, Interacting with a diversity of disciplines such as R&D , Quality Engineering, Regulatory Affairs, etc. + Independent organizational… more
- RTX Corporation (Andover, MA)
- …assist in process sustainment, improve product yield, develop new processes and device capabilities, and assist in the creation of new technology discriminators in ... Expected to work well in small, cross-functional teams, assist in pursuing contract R&D , and assist in transitioning processes into production. + May manage small… more
- Hologic (Marlborough, MA)
- …+ In-depth understanding of FDA Quality System Regulations, ISO 13485, and Medical Device Directive. + Expertise in compliance issues and regulatory ... Principal Quality Assurance Engineer Marlborough, MA, United States Louisville, CO, United...and compliance. **Experience:** + Minimum 12+ years in the medical device industry. + Proven track record… more
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