- GE HealthCare (Waukesha, WI)
- …including algorithm development, medical technology development, product development in the medical device industry. + Minimum of 5 years of experience ... **Job Description Summary** This Senior Director role reports to the CTO for Diagnostic...business development. + Proven experience with Software as a Medical Device (SaMD) development, including regulatory standards… more
- Edwards Lifesciences (Irvine, CA)
- …or related field with 15+ years of relevant Engineering experience with 10+ years in medical device -OR- + Master's degree in engineering or related field with ... R&D Engineering team, you will work closely with our Quality and Manufacturing teams to develop the latest tools...years of relevant Engineering experience with 10+ years in medical device + 5+ years of experience… more
- Guthrie (Sayre, PA)
- …of a physician-administrator leadership model. The dyad pairs the Executive Director of Research (physician leader-HPA) with a senior administrative executive to ... regulatory areas. + Supports research and scholarly activities related to Graduate Medical Education (GME), encompassing residents, fellows and medical students… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …complementary technology experience + Experience delivering technology solutions in a Medical Device or Pharmaceutical regulated environment + Solid knowledge ... Business Partner will report to the TGS Senior Director , Product Services and work with the Quality...of possible** BD is one of the largest global medical technology companies in the world. Advancing the world… more
- ThermoFisher Scientific (Carlsbad, CA)
- …organizational expertise, and **_deep industry knowledge across the pharmaceutical, biotech, or medical device sectors_** , along with a proven track record ... part of Thermo Fisher Scientific, as a **Sr Account Director /Executive Account Director , Business Development** **Biotech** and...key account management in a related Pharmaceutical, Biotech or Medical Device sales industry + Experience in… more
- IQVIA (Columbia, MD)
- …7+ years of regulatory affairs experience required. + 4+ years of cardiovascular medical device experience required. The ideal candidate will have direct ... MCRA an IQVIA business is seeking an Director , Cardiovascular Regulatory Affairs to be a critical...collaboratively with other MCRA departments, including clinical, reimbursement, and quality assurance. + Work with other regulatory leadership to… more
- Bausch + Lomb (Harrisburg, PA)
- …R&D/Project Management, Clinical/ Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, Pharmacovigilance/GPSS and Drug/ Device Safety, and ... areas to provide input on study-related documents and issues (DMP, SAP, drug/ device supplies, CSR, etc.). + Provides clinical operations input in the identification,… more
- Skyworks (Newbury Park, CA)
- …the way the world communicates. Requisition ID: 75609 Job Description The MSB Director DFT/DFM owns the end-to-end design quality strategy for MSB's highly ... Director , Engineering DFT/DFM Apply now " Date:Jul 10,...test coverage + Collaborate with the design and customer quality teams to ensure that lifetime testability is considered… more
- Edwards Lifesciences (Chicago, IL)
- …for (Preferred):** + Deep engineering experience, with a strong background in medical device development. Experience in implantable sensors for cardiac ... principles and practices + Knowledge and understanding of relevant medical device regulations (21 CFR Part 820),...matters of significance to the organization + Dedicated to quality client service and pro-active and responsive to client… more
- Olympus Corporation of the Americas (Westborough, MA)
- …of the typical functional roles and responsibilities in medical device organizations. + Practical understanding of global regulatory/ quality standards and ... 7 years of experience in a cross-functional project leadership role in the medical device industry, preferably leading due diligence and post-merger integration… more