- Abbott (Pleasanton, CA)
- …will work closely with cross-functional peers in quality, operation, marketing, clinical and regulatory , medical affairs , commercials to define an aligned ... levels in the organization. + Minimum of ten (10) years' experience in medical device development and/or other highly regulated industry + Previous experience… more
- CTG (Woodland, CA)
- …Biology preferred) **Qualifications** * Minimum 3 years' experience in Quality or Regulatory , preferably in medical device , pharmaceutical, or biotechnology ... II will develop and support all Quality Management System (QMS) and Regulatory Affairs (RA) activities in alignment with site quality goals and metrics. This… more
- Imperative Care (Campbell, CA)
- …directly with customer representatives, marketing, physicians, pre-clinical engineering, and regulatory affairs to understand user interactions, identify product ... discipline and a minimum of 8 years of related experience developing flexible medical device instruments; or equivalent combination of education and work… more
- Edwards Lifesciences (Irvine, CA)
- …multiple functions, including key stakeholders (eg, product management, convention management, clinical affairs , legal and regulatory affairs ), to ensure ... related experience working in digital marketing + Experience in the medical device , pharmaceutical or biotech industries **What else we look for (preferred):**… more
- Cardinal Health (Sacramento, CA)
- …will also help to support inorganic product opportunities and better define our medical device connectivity strategy. **_Responsibilities_** + Support and be a ... evolution + Collaborate with partners across enterprise, including R&D, Regulatory , Clinical Affairs , Sourcing, Manufacturing, Strategy Functions,...+ 4+ years experience in related field, preferred. + Medical device or global medical … 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. ... related field. 2. Minimum six (6) years of relevant work experience in medical device industry. 3. Minimum one (1) year of management experience. 4. Experience… 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 ... field 2. Minimum five (5) years of relevant work experience in medical device industry 3. Knowledge of and ability to use design/engineering and management… more
- Abbott (Alameda, CA)
- …and manage the digital health analytics + Work cross functionally with market access, regulatory affairs , medical and clinical resources to deliver on ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Danaher Corporation (Brea, CA)
- …risks. + Collaborate with cross-functional teams across R&D, Procurement, Operations, Quality, and Regulatory Affairs to embed quality into all phases of the ... would be a plus if you also possess : + Experience in FDA-regulated or medical device manufacturing environments. + Certifications such as CQE, CQA, Six Sigma,… more
- Envista Holdings Corporation (Pomona, CA)
- …whether to accept the product and future purchases from the vendor. + Supports Regulatory Affairs with their activities related to submissions and notified body ... related field; Master's degree preferred + 5+ years of experience in Engineering; medical device or similar regulated industry highly preferred + Strong… more