- Fujifilm (Harrisburg, PA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... responsibilities** + Performs the installation of hardware and software of medical imaging systems, components, and accessories to ensure conformance with… more
- Merck (West Point, PA)
- …and project management in the scale-up, development, commercialization, and transfer of medical devices and combination products, with a focus on autoinjectors, ... the development, commercialization, and transfer and sustained launch of medical devices and combination products globally. +...preferred. + Minimum of 10 years of experience in medical device or combination product engineering, with… more
- Fujifilm (Harrisburg, PA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... of up to 3 Tesla, which could dangerously affect any implanted medical devices made of ferrous material, potentially causing serious injury and/or death.… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …to meet regulatory / procedural deadlines. + Demonstrated working knowledge of Medical Device Quality Systems regulations including ISO 13485, 21CFR820, and ... (https://www.olympusamerica.com/careers) . **Job Description** Responsible for the review of medical device global complaints and coordinate the resolution… more
- ZOLL Medical Corporation (Pittsburgh, PA)
- …development of complex electronic and software systems required. + Experience with medical device development including regulatory requirements required. ... provide innovative technologies that make a meaningful difference in people's lives. Our medical devices , software and related services are used worldwide to… more
- Penn Medicine (Philadelphia, PA)
- …(CE) team, providing Clinical Engineering guidance around the implementation of medical devices and managing our Medical Device Cyber Security program. ... of healthcare. That involves interacting with clinicians, educators, networking, MDS (interfacing medical devices with other systems), regulatory , safety,… more
- Fujifilm (Harrisburg, PA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... with Key Accounts and Opinion Leaders within the Liver/Hepatology Medical Oncology community. Manage specific assigned geographic areas and successfully… more
- Wolters Kluwer (Harrisburg, PA)
- …and other software tools to for-profit corporations including CROs, pharma and medical device companies. The **Senior Account & Relationship Manager** will ... calling primarily on Librarians, Information Scientists, Heads of Global Regulatory Affairs, Directors of Medical Affairs, and...+ Proven track record selling into the pharmaceutical and medical device companies, and CRO's (preferred) +… 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
- University of Pennsylvania (Philadelphia, PA)
- …follow-up activities, performing phlebotomy to collect samples from patients, abstracting medical and demographics data from medical records, completing source ... managing the adverse event reporting process and assisting with the regulatory and financial management of multiple studies. Coordinate several investigational … more