- GE HealthCare (Waukesha, WI)
- …defining and executing innovative strategies for biocompatibility evaluation and risk analysis of medical devices in the GE HealthCare Imaging/ X-ray/ CT family ... **Job Description** **Roles and Responsibilities:** + Design and execute medical device biocompatibility strategies to assure user...+ Experience (10+ years) in design and development of medical devices that are categorized as FDA… more
- Terumo Medical Corporation (Elkton, MD)
- …(TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high-quality medical devices used in a broad range of applications for ... of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in...+ Knowledge of national and international regulations applicable to medical devices including Quality System Regulations, 21… more
- Terumo Medical Corporation (Elkton, MD)
- …(TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high-quality medical devices used in a broad range of applications for ... of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in...and compliance requirements in the design and manufacture of medical devices . The Systems Analyst, Manufacturing will… more
- Terumo Medical Corporation (Elkton, MD)
- …(TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high-quality medical devices used in a broad range of applications for ... TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide… more
- Terumo Neuro (Aliso Viejo, CA)
- …review, investigation, and assessment of adverse events. 5. Class III medical device safety experience. **External-Facing Title:** Specialist, Clinical Safety ... milestones and to provide regular progress updates. + Support clinical science and regulatory affairs functions by utilizing medical expertise to provide input… more
- WMCHealth (Suffern, NY)
- …annotates medical records in accordance with established procedures and regulatory requirements and provides information to clinical and support staff to ... updates specialized plans of treatment and preventive care regimens in accordance with medical orders and nursing standards, and also annotates medical records… more
- Merck (West Point, PA)
- …new product packaging development for vaccine and biologic dosage form products, including Medical Device and Combination Products (MDCPs) in the human health ... understanding and experience of unique requirements of packaging system development of Medical Device and Combination Products, including pre-filled syringes and… more
- Evolent (Helena, MT)
- …cases (eg, cardiac catheterizations, coronary interventions, endovascular procedures, implantable cardiac devices , etc) that do not initially meet medical ... calls) with requesting physicians or ordering providers, when available, within the regulatory timeframe of the request. + Utilizes medical /clinical review… more
- Medtronic (Northridge, CA)
- …management framework, ensuring compliance with ISO 10993 standards and global medical device regulations. This role involves conducting comprehensive ... related fields. MS or PhD preferred. + Strong understanding of ISO 10993 and global medical device regulations (eg, EU MDR, FDA, REACH, Prop 65). + Experience… more
- Cook Medical (Bloomington, IN)
- …across the organization by solving material problems to develop and improve medical devices and manufacturing processes while advancing the strategic goals ... departments on multiple large scale technical projects. Respond to regulatory material questions and adhere to the Quality Management...Polymer Science.2. Five (5) years of experience in the Medical Device Industry.3. One (1) year of… more