- Oracle (Boston, MA)
- …self-healing, and scalable processes. + Serve as the escalation authority for device performance, software/firmware issues, and field incidents. + Author ... roadmaps, investment cases, automation strategies, and device standardization documents. **KEY RESPONSIBILITIES:** + Develop, communicate, and execute the global… more
- Fresenius Medical Center (Lawrence, MA)
- **PURPOSE AND SCOPE** Act as a Quality Business Partner for Software as a Medical Device and Non- medical software device engineering teams to ensure ... judgment in selecting methods and techniques for obtaining solutions. . Networks with senior internal and external personnel in own area of expertise. . May escalate… 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 ... related to the SDLC. + Communicates significant issues to senior management, including appropriate containment and correction activities, as...+ Minimum of 6 years of experience in a medical device setting. + Experience in the… more
- Philips (Cambridge, MA)
- … Program Manager, you will lead high-impact programs that advance our medical device portfolio, elevate product performance, strengthen product quality & ... that drive product development, lifecycle management, and global execution across multiple medical device portfolios. + Develop and implement program and… more
- Hologic (Marlborough, MA)
- …and maintaining robust CI/CD infrastructure and development tools to support high-quality medical device software delivery. This role requires you to bridge ... - Marlborough, MA Marlborough, MA, United States As a Senior Software DevOps Engineer, you will be responsible for...SVN and Git, including migration strategies. + Familiarity with medical device software development standards and regulatory… more
- J&J Family of Companies (Danvers, MA)
- …or a related engineering discipline. + Minimum of 5 years of experience in medical device development ( senior -level candidates often have more). + ... | Winning Culture | Heart Recovery** Overview As a Senior Systems Engineer, you will own the design input...design controls and traceability practices. + Solid understanding of medical device regulatory environment and standards (for… more
- Candela Corporation (Marlborough, MA)
- …in engineering or related field , plus 15 years of related experience in the medical device industry with at least 12 years in a management/leadership role in ... quality / regulatory / compliance. . Working understanding of relevant global/regional medical device regulations and standards with particular emphasis on… more
- Dentsply Sirona (Waltham, MA)
- …Experience: + 5(+) years of experience in regulatory affairs, preferably in the medical device industry. + Experience with leading regulatory submissions and ... relationships. + Manages day to day activities for less senior Regulatory Affairs professionals, including but not limited to...13485, EU MDR). + Experience with software as a medical device , AI and/or medical … more
- Fujifilm (Boston, MA)
- … senior product manager, product/technical director). + Minimum 8 years of medical device experience with strong clinical background. + Prior experience in ... of product commercialization, including both upstream and downstream marketing. The Senior Product Manager, Interventional GI & Accessories contributes to the… more
- Cognizant (Boston, MA)
- …in Sales and Business development within Life Sciences, HealthTech, Medical Device industry + Bachelor's/Master's degrees in related field is preferred ... environment. This role will have a visible presence within the Life Sciences/ Medical Device industry representing Cognizant and our service offerings **Role**… more