- Cognizant (Tallahassee, FL)
- …+ Architecture & Design: Define site-level reference architectures, standardize device selections, and communicate complex technical concepts clearly to ... systems and devices. + Connectivity & Data Handling: Strong knowledge of device communication protocols and reliable data flow. + Networking & Security: Network… more
- Oracle (Tallahassee, FL)
- …Minimum 7 years' experience in clinical leadership roles within medical device , digital health, or regulated healthcare software sectors. . Extensive ... process, especially for products newly classified under stricter EU medical device rules. . Knowledge of software development processes (including agile… more
- IQVIA (Orlando, FL)
- …without patient care responsibilities. You will be at the forefront of cutting-edge medical device technology and gain professional growth and exposure to ... medical device industry If you have a...and requires only a username and password. The entire application takes 5-7 minutes to complete. **Job Description:** Our… more
- Cardinal Health (Tallahassee, FL)
- …ability to develop high-quality clinical documents. Extensive knowledge of the European medical device guidelines/regulations such as MEDDEV and MDD/MDR is ... analysis & regulatory requirements. + Experience working within a medical device or pharmaceutical organization in a...+ Proficient in using EndNote or other reference manager software + Strong data extraction and analysis skills +… more
- Oracle (Tallahassee, FL)
- …self-healing, and scalable processes. + Serve as the escalation authority for device performance, software /firmware issues, and field incidents. + Author ... roadmaps, investment cases, automation strategies, and device standardization documents. **KEY RESPONSIBILITIES:** + Develop, communicate, and execute the global… more
- Fujifilm (Tallahassee, FL)
- …enterprise quotes. + Understand the specialized requirements for quoting regulated medical software , hardware, and consulting; ensuring accurate compliance, ... + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
- SHI (Tallahassee, FL)
- … + Responsible for the design and implementation of Microsoft Intune device management solutions and related technologies based on customer requirements including: ... + Microsoft Intune + Windows, macOS, mobile deployment + Apple Automatic Device Enrollment + Android Zero Touch + Autopilot + Manual enrollment scenarios +… more
- City of Jacksonville (Jacksonville, FL)
- …If you answered "yes" to any of these questions, you need to complete your application now. Work for the city you love The Parks, Recreation and Community Services ... personal computers using Microsoft, spreadsheet, database and other related software , peripheral and electronic devices, hand-held computer, computerized citation… more
- Fujifilm (Tallahassee, FL)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... is responsible for performing upgrades for Fujifilm Healthcare Americas Corporation (HCUS) Medical Informatics (MI) products to all eligible sites. In addition will… more
- Dentsply Sirona (Sarasota, FL)
- …of FDA 510(k) and international regulations (eg, EN ISO 13485, EU MDR). + Experience with software as a medical device , AI and/or medical devices ... years of experience in regulatory affairs, preferably in the medical device industry. + Experience with leading... software is a plus Required Computer / Software Skills: + Proficiency with Microsoft Office Suite +… more