- Abbott (Alameda, CA)
- …is located in Alameda, California.** **What you'll do:** + Conduct single or multi-center medical device clinical studies. + Perform study site visits (SQV, SIV, ... of relevant experience in site monitoring. + Experience in conducting medical device and/or _in-vitro_ diagnostics studies preferred. Pharmaceutical background… more
- Gilead Sciences, Inc. (Foster City, CA)
- …+ Collaborate with cross-functional teams, including manufacturing, quality control, and regulatory affairs , to design SAP BRH solutions that optimize ... deep expertise in SAP BRH & SAP QM module, regulatory compliance (such as GxP and FDA), and life...particularly in regulated environments such as pharmaceutical, biotech, or medical device manufacturing. + Experience with SAP… more
- Wolters Kluwer (Sacramento, CA)
- …Manager** will be calling primarily on Librarians, Information Scientists, Heads of Global Regulatory Affairs , Directors of Medical Affairs , and ... software tools to for-profit corporations including CROs, pharma and medical device companies. The **Senior Account &...+ Proven track record selling into the pharmaceutical and medical device companies, and CRO's (preferred) +… more
- Abbott (Alameda, CA)
- …monitor the performance of marketing programs, and adjust tactics as needed + Partner with Regulatory Affairs , Medical Affairs , Legal, and OEC colleagues ... of 4-6 years of experience in product marketing in healthcare, pharmaceutical, medical device , or a regulated industry. **Preferred Qualifications** + MBA… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …close partnership with R&D, Enterprise Security, Technology & Global Services, Quality, Regulatory Affairs , Legal, business leaders and functional authorities at ... help BUs deliver best-in-class secure products, consistent with global regulatory requirements over the lifecycle. This role works in...that will mitigate risk + Solid understanding of the medical device and healthcare IT space +… more
- J&J Family of Companies (Irvine, CA)
- …study team; + Cooperates with cross-functional teams (Research & Development, Complaint Handling, Quality/ Regulatory , Medical Affairs , Medical Safety) to ... of clinical safety data with the clinical study team, Medical Affairs or Medical Safety...+ Clinical/ medical background is a plus. + Medical device experience is highly preferred. +… more
- Edwards Lifesciences (Santa Ana, CA)
- …surgery or interventional cardiology are strongly preferred; candidates with other relevant medical device clinical sales support experience will be considered + ... Director and will collaborate with multiple departments including Sales, Clinical Affairs , Marketing, Quality, Regulatory , and Education. After extensive… more
- Abbott (Sylmar, CA)
- …functions such as compliance, legal, contracts & pricing, procurement, legal operations, regulatory affairs , governmental affairs , audit, and/or finance. + ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- AbbVie (South San Francisco, CA)
- …science or a related field with relevant experience in pharma, academia, healthcare and/or medical device industries; MBA or consulting experience a plus. + MS ... Stakeholders Digital Science Team, Therapeutic Areas, Clinical Development, HEOR, PMed, Medical Affairs , Patient Safety Additional Information Applicable only to… more
- Abbott (San Diego, CA)
- …+ Minimum 15 years of experience in software development, preferably in a medical device /diagnostics or other regulated environment. Direct experience with IVD ... + Minimum 20 years of experience in software development, preferably in a medical device /diagnostics or other regulated environment. Direct experience with IVD… more