- Abbott (Alameda, CA)
- …data to drive better-informed decisions. We're revolutionizing the way people monitor their glucose levels with our new sensing technology. **The Opportunity** ... This **Regulatory Affairs Manager** will work on- site in Alameda, CA for our Diabetes Care Division....to drive better-informed decisions. We're revolutionizing the way people monitor their glucose levels with our new sensing technology.… more
- Edwards Lifesciences (Irvine, CA)
- …Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical ... submissions. May interact with regulatory agencies as part of submission review and on- site audit support. (eg, IDE's, PMA's, annual reports, 510(k)'s, STED's and CE… more
- Edwards Lifesciences (Irvine, CA)
- …boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. It's our driving force to help patients live longer and ... submissions. May interact with regulatory agencies as part of submission review and on- site audit support. (eg, IDE's, PMA's, annual reports, 510(k)'s, STED's and CE… more
- Charles River Laboratories (Hollister, CA)
- … site Leadership Team and conduct reviews at appropriate intervals with facility senior management. + Consult with site management and employees on Federal, ... service firms, evaluating proposals, conducting interviews and making recommendations to senior management, in partnership with site Procurement and Management… more
- Bristol Myers Squibb (San Diego, CA)
- …leadership role spans cross-functional teams-including Commercial, Medical Affairs, Clinical Operations, Early Development, and Manufacturing-with a sharp focus ... operational insights. + Define integration strategy across enterprise applications ( clinical , ERP, CRM, manufacturing, compliance) balancing traceability, integrity, and… more
- Abbott (Sylmar, CA)
- …manufactured or distributed to meet required legislation. The individual has department/group/ site level influence and is generally recognized as an expert resource ... + Provide regulatory input to product lifecycle planning + Monitor regulatory outcomes of initial product concepts and provide...outcomes of initial product concepts and provide input to senior regulatory management + Assist in the development of… more
- IQVIA (Valencia, CA)
- …with pathology findings. Release timely reports into LIMS for sponsor and/or clinical site action. Participate in or initiate internal and client-facing ... impacting pathology interpretations. Perform microscopic analyses of laboratory assays and monitor digitization of slides. Correlate clinical information… more
- Ventura County (Ventura, CA)
- …Provides medical direction and administration including, but not limited to, developing clinical practice guidelines. + Monitor the quality and appropriateness ... in one or more Federally Qualified Health Center (FQHC) site . WHAT WE OFFER The County of Ventura offers...is responsible for fostering a culture of collaboration, teamwork, clinical excellence, and superior operational performance, and they work… more
- Boehringer Ingelheim (Fremont, CA)
- …the status to the site 's appropriate review forums that may include site senior leadership personnel. + Performs additional duties as assigned within the ... of the Biopharma GxP relevant material/service suppliers, including services of clinical and commercial GMP contract manufacturing organizations (CMOs) and contract… more
- IQVIA (San Francisco, CA)
- _On behalf of our partner, Health Monitor , IQVIA is assisting with the recruiting process for a direct hire role with Health Monitor ._ Company Overview For over ... 450,000 healthcare professionals engaging with our omnichannel educational products. Health Monitor delivers premium point of care content that empowers patients and… more