- Edwards Lifesciences (Salt Lake City, UT)
- …engineering or related field, with experience in Quality Engineering, Quality Management, or Regulatory Compliance within the medical device industry; prior ... ensuring a culture of quality and compliance with global regulatory requirements. **How You'll Make an Impact:** + Manage...for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination… more
- Abbott (Lake Forest, IL)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... privacy laws and other laws and regulations pertaining to the diagnostics, pharmaceutical, or medical device industries. * Diagnostics, medical device ,… more
- Bausch + Lomb (Kirkwood, MO)
- …60601-1), medical device design control (ISO 13485), risk management for medical devices (ISO 14971), and regulatory requirements for Class II ... Key Responsibilities: + Review and analyze legacy Class II medical device system documentation for acquired ...electronic medical devices . + Successful experience with design documentation, DHF/DMR structure,… more
- University of Rochester (Rochester, NY)
- …quality and regulatory compliance with investigational products for biologics and medical devices preferred. **KNOWLEDGE, SKILLS & ABILITIES** + Proven track ... Ensures compliance with Good Clinical Practices (GCP) and national and international regulatory requirements specific to the biopharma and medical technology… more
- AbbVie (North Chicago, IL)
- …PhD and typically 4 years of experience. + Proven experience with medical devices , combination products, or the pharmaceutical industry, including hands-on ... R&D Device and Combination Product Development (DCPD) function provides device development expertise for Aesthetic Devices and Therapeutic Combination… more
- Immigration and Customs Enforcement (District Of Columbia, DC)
- …recommendations for system enhancements. Oversee acquisition, management, and training for medical devices integrated into the EHR, ensuring alignment with ... EHR configuration, including clinical workflows, CDSS, order sets, and integration of medical devices . Experience with clinical workflows in healthcare or… more
- Fujifilm (Wayne, NJ)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... but will consider applicants with repair experience in electronics, medical device , mechanical, or a similar field....handle or feel objects, use electronic or mechanical repair devices , fine motor skill dexterity, reach with hands and… more
- Bausch + Lomb (St. Louis, MO)
- …60601-1), medical device design control (ISO 13485), risk management for medical devices (ISO 14971), and regulatory requirements for Class II ... verification of electronic systems for Class II and III medical devices , responsible for the quality and...implementation of electronics hardware for complex electromechanical and embedded medical device in emerging designs + Provide… more
- Sanofi Group (Cambridge, MA)
- …delivery of Drug Device Combination Products and Medical Devices . Working within strict technical, scientific, and regulatory frameworks, you manage ... possible. Ready to get started? **Main Responsibilities** + Develops medical devices and drug device ...Develops medical devices and drug device combination products following regulatory requirements (FDA,… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …through immersive learning focused on the key role quality plays at BD and in the medical device industry to advance the world of health and ensure the safety of ... closely with Quality Engineers and cross functional teams including Manufacturing, R&D, Regulatory Affairs, and Medical Affairs. In every rotation, associates… more