- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... ultrasound research or a PhD (preferred). + Ultrasound based medical device product development is highly preferred....of data (eg Minitab or R). + Experience in medical devices using shock waves or lithotripsy… more
- Abbott (Alameda, CA)
- …and preventative action of medical devices , including software as a medical device (SaMD), in-vitro, diagnostic devices , consumer devices , and ... Device Master Record (DMR) are in compliance with regulatory standards and quality management policies and procedures. +... devices or pharmaceutical products. + Knowledge of medical device standards including FDA QSR, ISO… more
- Merck (West Point, PA)
- …complex technical projects and/or equipment technology assessments within the packaging and Medical Devices & Combination Products (MDCP) space as part of ... and Qualifications:** + Minimum of 10 years' experience in the pharmaceutical, biotechnology, or medical device industry, with at least 3-5 years in a leadership… more
- Medtronic (Mounds View, MN)
- …plays a critical role in ensuring the security of Medtronic Surgical Operating Unit medical device solutions. Reporting to the Director of Product Security, this ... and digital solutions. This role focuses on cybersecurity for medical devices and embedded systems. It is...impact by exploring a career with the world's leading Medical Device company, striving "to alleviate pain,… more
- Zimmer Biomet (Englewood, CO)
- … device from ideation to commercialization required. * Understanding of medical device industry regulatory requirements preferred. * Experience with ... meaningful projects that focus on design and development of medical devices and development life cycle with...engineering discipline with 3-7 years of development experience in medical device . * Prior experience in taking… more
- Cook Medical (Bloomington, IN)
- …agencies related to material information* Track material compliance requirements with appropriate medical device standards and regulations* Serve as a technical ... of ISO 10993 and chemical characterization* In-depth knowledge of common medical device materials (polymers) and additives* Experience with analytical… more
- Candela Corporation (Marlborough, MA)
- …that meets internal quality requirements and regulatory standards for Class I/II medical devices (FDA 21 DFR 820.30, ISO 14791, IEC 62304, IEC 62366) ... **Company Overview:** Candela Corporation is a leading global aesthetic device company with a comprehensive product portfolio and a..., EU, IEC, AAMI, and ANSI standards relating to medical devices (eg ISO 13485, IEC 60601,… more
- Stryker (Portage, MI)
- …Science. + Experience with regulatory agencies (FDA, MoH, TUV) and medical device regulations (820, IEC 62304/82304, 60601), with experience in Software ... 's Digital Health division and portfolio Software as a Medical Device (SiMD) or Software in a...+ Partner with cross-functional teams, including marketing, R&D, clinical, regulatory , and operations, to deliver quality, compliant products. +… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …experience, including a minimum of 5-7 years in the pharmaceutical/biotechnology or medical device industry. + In-depth knowledge of (US) healthcare systems, ... track record of working in Health Economics & Market Access, Reimbursement for medical devices . + Track record of working effectively with other cultures… more
- Fujifilm (Frankfort, KY)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... + Ability to work effectively with customers in the medical field. + Ability to prioritize and handle multiple...a discipline is a plus. + Exposure to the medical field, particularly cardiology, is a plus. + Some… more