- Olympus Corporation of the Americas (Westborough, MA)
- …+ Excellent understanding of the typical functional roles and responsibilities in medical device organizations + Demonstrated ability to work cross-functionally, ... Every day, we live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care so people everywhere can fulfill… more
- Olympus Corporation of the Americas (Westborough, MA)
- …+ Excellent understanding of the typical functional roles and responsibilities in medical device organizations + Demonstrated ability to work cross-functionally, ... live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care...the inorganic strategy goals. They are accountable for a high- quality due diligence report and integration strategy/plan, and to… more
- Fujifilm (Boston, MA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... policies, and procedures. + Effective communication within FUJIFILM IVD organization of sales, quality and compliance issues. + Utilization of the IVD reporting… more
- TE Connectivity (Boston, MA)
- …of high-performing technical and/or complex organizational leadership experience preferred + Medical device sales and/or product management experience preferred ... for all accounts within their territory. Responsible for promoting the technology of TE Medical Business Unit and position TE Medical for a long-term growth.… more
- Medtronic (Newton, MA)
- …+ Background in electrophysiology, cardiac ablation, or adjacent fields within the medical device industry. + Demonstrated experience leading highly technical ... and quality assurance of software systems, applications, and tools, ensuring compliance with regulatory and quality standards. + Drive continuous improvement… more
- Integra LifeSciences (Braintree, MA)
- …discipline. + A minimum of 2-4 years' experience in a medical device , pharmaceuticals, Quality /Regulatory Compliance , or other cGMP regulated product ... Technician II** will be responsible for performing environmental monitoring, quality control microbiological laboratory testing of in-process, finished goods,… more
- Boston Engineering Corporation (Waltham, MA)
- …embedded or desktop applications + Mobile app development + Strong familiarity with medical device software development standards (eg, IEC 62304) and the product ... systems. + Comfortable working under ISO 9001 and ISO 13485 quality systems; familiarity with documentation, traceability, and compliance requirements.… more
- J&J Family of Companies (Danvers, MA)
- …of 5 years of experience in equipment engineering, preferably in the medical device manufacturing industry. + Extensive experience with production manufacturing ... OQ, PQ validation processes and Good Manufacturing Practices (GMP) for building medical devices. This position requires an individual who can work independently and… more
- Medtronic (Boston, MA)
- …technical information to both technical and non-technical audience. * Experience in medical device or regulated industry software development is preferred. * ... In the Surgical Robotics (SR) business, part of Medtronic's Medical Surgical Portfolio, we believe patients around the world...we believe patients around the world deserve access to quality care and improved outcomes. We strive to expand… more
- AbbVie (Worcester, MA)
- …21 CFR Part 11 requirements for automated systems in the pharmaceutical or medical device industries. + Demonstrated problem solving skills and innovative ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...platform like POMS. + Conversant with industry standards on quality and regulatory compliance requirements such as… more