- Abbott (Alameda, CA)
- …design experience preferred + Detailed experience with medical device development processes and FDA 510K and PMA regulatory requirement and process is desirable. ... Abbott is a global healthcare leader that helps people live more fully...design control procedures for software development in accordance with FDA guidelines. + Lead software development projects, providing mentoring… more
- Cedars-Sinai (Los Angeles, CA)
- …for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for ... study budget and patient research billing. Ensures compliance with all federal, local, FDA , IRB, and HIPAA guidelines and regulations pertaining to the study and… more
- Medtronic (Los Angeles, CA)
- …operating room, so healthcare /surgical setting experience + Familiarity with FDA product requirements and regulatory guidelines + Experience with robotics ... life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with...understand schematics and engineering drawings + Familiar with the FDA 21 CFR, CGMP for Medical devices + Demonstrable… more
- Medtronic (Irvine, CA)
- … healthcare industry. + Strong understanding of cybersecurity frameworks, regulatory requirements, risk management, and industry best practices (eg, HIPAA, NIST, ... can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down… more
- Abbott (Sylmar, CA)
- … requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures, ... Abbott is a global healthcare leader that helps people live more fully...systems are developed, validated and maintained in compliance with regulatory and business procedures. As a global leader in… more
- Abbott (Milpitas, CA)
- …highly desirable + Detailed experience with medical device development processes and FDA 510K and PMA regulatory requirement **Preferred Qualifications** + Good ... Abbott is a global healthcare leader that helps people live more fully...the development, verification, ensuring timely delivery and adherence to FDA -compliant design control procedures. They provide technical leadership, mentoring,… more
- Abbott (Alameda, CA)
- …is highly desirable + Detailed experience with medical device development processes and FDA 510K and PMA regulatory requirement + Preferred team leadership ... Abbott is a global healthcare leader that helps people live more fully...the development, verification, ensuring timely delivery and adherence to FDA -compliant design control procedures. They provide technical leadership, mentoring,… more
- Owens & Minor (Fairfield, CA)
- At Owens & Minor, we are a critical part of the healthcare process. As a Fortune 500 company with 350+ facilities across the US and 22,000 teammates in over 90 ... of what we do. Our mission is to empower our customers to advance healthcare , and our success starts with our teammates. Owens & Minor teammate benefits include:… more
- Stryker (San Jose, CA)
- …improvement across the software lifecycle by implementing software industry best practices and regulatory standards ( FDA , TGA, EUMDR, IT). + Engage in design and ... Google, Microsoft, or similar, demonstrating strong technical skills + Experience with regulatory agencies ( FDA , MoH, TUV) and medical device regulations (820,… more
- Cedars-Sinai (Los Angeles, CA)
- …US News & World Report. From working with a team of committed healthcare professionals to using state-of-the-art facilities, you'll have everything necessary to do ... all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board (IRB). **Primary Job Duties and… more