- Olympus Corporation of the Americas (Westborough, MA)
- …21 CFR 820 and ISO 13485 required. + Working knowledge of international medical device quality system requirements required. + Complete understanding and ... and early morning teleconferences. **Preferred:** + MBA Preferred. + Medical Device Experience preferred + Black Belt...Posting Notes: || United States (US) || Massachusetts (US-MA) || Westborough || Quality & Regulatory Affairs … more
- Teleflex (San Francisco, CA)
- …an optimal customer experience. Collaborating with Marketing, Sales, Engineering and Clinical & Medical Affairs on key projects and initiatives, the CSS utilizes ... innovation, our Arrow brand of technically advanced vascular access devices are renowned throughout the world. Many of our...**Specialized Skills / Other Requirements** + 2+ years of Medical Device Industry experience. + 3+ years… more
- Teleflex (Albany, NY)
- …an optimal customer experience. Collaborating with Marketing, Sales, Engineering and Clinical & Medical Affairs on key projects and initiatives, the CSS utilizes ... innovation, our Arrow brand of technically advanced vascular access devices are renowned throughout the world. Many of our...**Specialized Skills / Other Requirements** - 2+ years of Medical Device Industry experience. - 3+ years… more
- Terumo Neuro (Aliso Viejo, CA)
- …operation process/documentation. Ensure seamless coordination across functions, particularly with R&D, Regulatory Affairs , Compliance, and TIS marketing teams to ... operations, or commercial support. 3. Experience in healthcare, biotech, or medical device industry. 4. Strong project coordination and written and verbal… 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. Knowledge of… more
- Teleflex (Morrisville, NC)
- …representative during acquisitions, collaborating with teams in Quality Assurance, Regulatory Affairs , Supply Chain, Design, and Manufacturing. Additionally, ... preferred - 5-10 years of experience working within an FDA regulated industry, Medical Device preferred - Advanced problem solving and root cause analysis… more
- Meta (New York, NY)
- …a scientific discipline or equivalent work experience 6. 3+ years of industry experience in medical device regulatory affairs or related industry 7. ... regulatory affairs specialist to join our medical devices compliance team. You will get...get to work on wearables and Software as a Medical Device (SaMD) applications for the US… more
- Stryker (Redmond, WA)
- … Regulatory Affairs ). + Previous experience with US Class II/III medical devices . + Experience authoring regulatory submissions for product approval. ... based **Hybrid** in **Redmond, Washington.** As part of the Medical Regulatory Affairs team, you...team, you will work with the team to maintain medical devices on the market and ensure… more
- Terumo Aortic (Sunrise, FL)
- …(or related field) from an accredited college or university and 3 years direct experience in medical device regulatory affairs + Minimum 5 years direct ... experience in medical device regulatory affairs if no...and Design Dossiers/Technical files) for Class II and III medical devices and a successful track record… more
- Medtronic (Irvine, CA)
- …from an accredited college or university required. + Minimum of 4 years of experience in medical device regulatory affairs + Or advanced degree with a ... minimum of 2 years of experience in medical device regulatory affairs **Nice To Have** + Excellent technical knowledge of medical products and… more
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