- GRAIL (Menlo Park, CA)
- …experience in managing clinical trials at a sponsor company (pharma, biotech, or medical device ) with a strong track record of successful trial initiation ... executed within compliance of regulations and of the highest quality , and to be able to identify areas of...in vitro diagnostics (IVD) highly preferred; pharmaceutical, biologics or medical device experience also acceptable + Thorough… 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 ... Purpose AbbVie's Digital Science Team is an innovative group that combines medical knowledge, digital technologies, regulatory , and data science expertise to… more
- Actalent (Sunnyvale, CA)
- …Design Engineer - DFX & Product Development Our client, a leading innovator in the medical device space, is seeking a Mechanical Design Engineer with a strong ... regulatory , and engineering Required Skills & Experience + Proven experience in medical device design and development + Strong knowledge of DFX, DFM,… 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 + ... will collaborate with multiple departments including Sales, Clinical Affairs, Marketing, Quality , Regulatory , and Education. After extensive training, a Field… more
- Terumo Neuro (Aliso Viejo, CA)
- …2. Minimum six (6) years of direct clinical research experience, preferably in the medical device industry, including at least two (2) years of monitoring ... various therapeutic areas (preferred areas: Neurovascular and/or Cardiovascular). 3. Experience in the medical device industry. 4. At least two (2) years of… more
- Veterans Affairs, Veterans Health Administration (Palo Alto, CA)
- …Veterans Integrated Services Network Advisory Board, Clinical Product Review, Reusable Medical Device , Environment of Care Rounds, and Enterprise Equipment ... outcomes. Provides health system-wide leadership for critical and semi-critical Reusable Medical Device (RDM), including sterile storage, reprocessing, standard… more
- Charles River Laboratories (Northridge, CA)
- …and abilities to perform the job (comparable to 2 years of biotech, medical device , pharmaceutical development, or project management) or equivalent combination ... across internal workflows. + Collaborate with departments such as R&D, Quality , Regulatory , and Manufacturing to meet project goals. + Ensure projects adhere… more
- Medtronic (Santa Ana, CA)
- …and all phases of the Product Development Process (PDP). Responsible for Medical Device Design specifically in Bioprosthetic heart valves, including prototyping ... regulatory requirements. Document design within applicable Design Control, Quality and Regulatory requirements. Conduct design verification and validation… more
- California Energy Commission (Sacramento, CA)
- …In addition to evaluating each candidate's relative ability, as demonstrated by quality and breadth of experience, the following factors will provide the basis ... State and federal environmental and energy law, including the California Environmental Quality Act;? 2. The rules governing the conduct of administrative hearings… more
- Terumo Neuro (Aliso Viejo, CA)
- …of ten (10) years of relevant manufacturing process development experience in the medical device industry. 3. Strong written and verbal communication skills. 4. ... of twelve (12) years of relevant manufacturing process development experience in the medical device industry. 3. Ability to design, develop, and validate… more