- Stryker (Fort Lauderdale, FL)
- …6 years demonstrated successful sales experience. + Minimum of 4 years related medical device experience. + Great communication skills. + Maintain all ... earn commission and/or bonuses + benefits. \#LI-REMOTE Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical… more
- J&J Family of Companies (Tampa, FL)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... studies and market releases. + Product knowledge including product vigilance and medical device reporting. + High attention to detail and accuracy. + Computer… more
- Kelly Services (Jacksonville, FL)
- …optimize control systems for advanced automated manufacturing equipment in a regulated medical device environment. You will be instrumental in improving ... comply with FDA regulations, ISO standards, and GMP requirements specific to medical device manufacturing. + **Documentation & Validation** Generate and maintain… more
- Medtronic (Jacksonville, FL)
- …ensure seamless integration and compliance. + Develop and review documentation according to medical device regulatory standards (eg, IEC 62304). + Conduct code ... with C and C++. + Developed and reviewed documentation according to medical device regulatory standards (eg, IEC 62304). + Proven track record of leading… more
- IQVIA (Jacksonville, FL)
- …with healthcare professionals and advocate for the well-being of patients through medical device technology. **You will be responsible for training and ... education and in-servicing to nurses, physicians, and hospital staff to support medical device implementations + Assess customer-specific education needs and… more
- Philips (Orlando, FL)
- …a minimum of 5+ years' experience in Quality Engineering within FDA regulated medical device environments, with proven expertise in Corrective and Preventive ... and data/trend. Analysis. + You have detailed knowledge of appropriate global medical device regulations, requirements and standards including 21 CFR Parts… more
- Dentsply Sirona (Sarasota, FL)
- …Experience: + 5(+) years of experience in regulatory affairs, preferably in the medical device industry. + Experience with leading regulatory submissions and ... regulations (eg, EN ISO 13485, EU MDR). + Experience with software as a medical device , AI and/or medical devices containing software is a plus Required… more
- IQVIA (Orlando, FL)
- _IQVIA has an opportunity with one of the largest medical device manufacturers in the US. We welcome you to apply if interested! You will be asked to create an ... experience by collaborating with healthcare professionals and leading technical initiatives in medical device technology. You will be responsible for leading a… more
- Oracle (Tallahassee, FL)
- …Oracle Health Data Intelligence is entering a high-impact phase of **MDR ( Medical Device Regulation)** readiness and **regulatory transformation** . Over the ... (Regulatory / Health Tech)** + Experience with one or more of: + MDR ( Medical Device Regulation) + ISO 14971 (risk management) + ISO 13485 + IEC 62304 +… more
- Oracle (Tallahassee, FL)
- …role will help ensure **operational alignment with international compliance frameworks and medical device regulatory requirements** as HDI scales its solutions ... Certification:** Collaborate with legal, regulatory, and product stakeholders to support ** medical device certification and compliance activities** as HDI… more