- J&J Family of Companies (Danvers, MA)
- …a related field. + 10+ years of experience in process validation within the medical device industry, with a focus on electro-mechanical systems. + Demonstrated ... manufacturing lines, and process changes. + Collaborate with Manufacturing and Quality Engineering to ensure validation requirements are integrated into design and… more
- Bristol Myers Squibb (Devens, MA)
- …System support strategy that integrates process knowledge, equipment design, and quality standards with information technology to reduce down-time, elevate the level ... of regulatory compliance, and introduce efficiency gains through effective use...of manufacturing equipment/devices to the Control System and troubleshooting device communication. + Understanding of engineering documentation such as… more
- Philips (Cambridge, MA)
- …a plus. + You have 4+ years in a role associated with healthcare and/or medical device and software development in a regulated environment. + You have experience ... teams to prioritize claims based on market trends and regulatory requirements. Continuously optimize strategy through analysis of competitor activity,… more
- Nanobiosym, Inc. (Cambridge, MA)
- …engineering grade resins a must More than 10 years experience Must have medical device experience, disposables preferred. familiar with ISO13485 and 14971 Must ... to be hands on and wear multiple "hats". -be ready to participate in quality systems, engineering, mfg, regulatory activities, etc. Individual would be a… more