- Fujifilm (Olympia, WA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... **Duties and responsibilities** + Performs hardware and software evaluation of medical imaging systems, components, and accessories to ensure conformance with… more
- Fujifilm (Des Moines, IA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... Knowledge Base articles. + Maintains an expert working knowledge of current medical imaging products and related technologies. + Engineers must have the ability… more
- 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 ... closely and partners with internal departments to efficiently deliver safe and effective medical device designs for manufacturing, which are in line with… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …+ Strong command of Quality Management Systems (QMS), ISO standards, GMP, USP-EP, and regulatory requirements applicable to medical devices + At least 5 ... of possible** BD is one of the largest global medical technology companies in the world. Advancing the world...Change Requests (BD- or Customer-Initiated)** + Stays informed of regulatory developments and advises BD and customers on their… more
- Integra LifeSciences (Braintree, MA)
- …with building management systems (BMS) and automated environmental controls. + Knowledge of regulatory requirements in the medical device or pharmaceutical ... 5-10 years of experience in experience in refrigeration maintenance, preferably in a medical device or regulated manufacturing environment. + Strong knowledge of… more
- Penn Medicine (Philadelphia, PA)
- …Responsibilities: + Under close supervision, maintains, repairs, and calibrates patient care medical devices , using general knowledge of lowrisk equipment. + ... sources of replacement materials required to service and maintain medical devices within the facilities. + Maintains...medical hardware, software and equipment products + Understand medical device usage within a health system… more
- US Tech Solutions (Thousand Oaks, CA)
- …yet practical solutions to meet those needs + Experience with combination products and device regulatory requirements and medical device development and ... engineering **Preferred Traits:** + Passion for proactively identifying opportunities through creative modeling and data analysis + Transform ambiguous business and technical questions into measurable and impactful projects + Partner with multi-discipline… more
- Bayer (Indianola, PA)
- …Agile methodology; + Prior internship experience in technical writing ability; + Knowledge of medical device regulatory processes. Employees can expect to be ... and develop written computer-based requirements (system, software, etc.) for medical device software development programs/products, including: + Application… more
- Fujifilm (Bothell, WA)
- …positive relationships + Experience with medical device development & medical device regulatory requirements is desirable but not required ... 6-8 years' experience as an electrical design engineer in the medical device or consumer electronic industry + Experience performing complex product development,… more
- Astrix Technology (Boston, MA)
- …field-based medical affairs role within the pharmaceutical, biotechnology, or medical device industry. + Scientific Expertise: Deep understanding of ... Collaboration: Work closely with internal teams such as Clinical Development, Regulatory Affairs, and Commercial to provide medical insights that… more