- Stryker (Sacramento, CA)
- …clinical data. + Form and justify conclusions regarding the overall benefit-risk profile of medical devices , in collaboration with a medical expert and other ... + years of industry experience in clinical, quality, or regulatory affairs (risk management, design quality, post-market...3 years of experience in writing clinical evaluations for medical devices required. + Demonstrated ability to… more
- Terumo Neuro (Aliso Viejo, CA)
- …functionally with Associates across all departments in R&D, Operations, Quality, and Regulatory Affairs to achieve company objectives and resolve project issues. ... Minimum six (6) years of relevant work experience in medical device industry. 3. Minimum one (1)...product development and project management of embedded software/firmware for medical devices . 6. Knowledge of and ability… more
- Abbott (Alameda, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... combination of appropriate education and experience. + Experience working on medical device studies and/or in-vitro diagnostics studies preferred. Pharmaceutical… more
- Abbott (Sylmar, CA)
- … Regulatory Compliance/ Affairs experience in In Vitro Diagnostics and medical device manufacturing or other similarly regulated environment. + Knowledge ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Abbott (Pleasanton, CA)
- …+ Two (2) years of Quality Systems, Quality Assurance and/or Regulatory Compliance/ Affairs experience in medical device manufacturing or other similarly ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Stryker (Fremont, CA)
- …do:** **Technical Responsibilities:** + Works with Divisional Leadership, KOLs, Marketing, Clinical Affairs and Regulatory Affairs and regional organizations ... internal stakeholders. + Works with Divisional Leadership, Marketing, Clinical Affairs and Regulatory Affairs and...desired):** **Preferred Skills** **/ Tools:** + Deep experience in medical device clinical research + 10+ years… more
- Abbott (San Diego, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... * Minimum 15 years of experience in software development, preferably in a medical device /diagnostics or other regulated environment. Direct experience with IVD… more
- Actalent (Irvine, CA)
- …will play a crucial role in ensuring the quality and compliance of new medical device products throughout their development lifecycle. You will be responsible ... plans and conducting risk reviews. Essential Skills + Experience with the medical device product development lifecycle, including risk management and… more
- Edwards Lifesciences (San Francisco, 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
- Edwards Lifesciences (Sacramento, CA)
- …Knowledge and understanding of Edwards policies, procedures, and international and domestic medical device regulatory guidelines relevant to clinical ... patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you… more