- US Tech Solutions (San Bruno, CA)
- …for medical devices , specifically focusing on Software as a Medical Device (SClient) or low-risk enforcement discretion products. 2. At least 3-5 ... Quality System Regulations, ISO 13485, and integration of best practices from the medical device industry. **Documentation and Support:** 1. Support the creation… 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 ... Device Master Record (DMR) are in compliance with regulatory standards and quality management policies and procedures. +...5+ experience in Software Quality Assurance. + Knowledge of medical device standards including FDA QSR, ISO… more
- Cook Medical (West Lafayette, IN)
- …of medical writing tasks). Qualifications MD or DO with medical device experience preferred; however, nurse practitioners and physician assistants ... 9-to-5 Eastern Standard Time schedule (Monday through Friday). Responsibilities Provide medical review of clinical and certain regulatory documents (including… more
- Hologic (San Diego, CA)
- …The ideal candidate plays a key role in ensuring the safety, effectiveness, and regulatory compliance of medical devices after release. The ideal candidate ... product complaints in compliance with Hologic SOPs and applicable regulatory requirements (FDA, ISO, EU MDR). + Conduct initial...in post-market quality assurance within the medical device industry such as medical devices… more
- Edwards Lifesciences (Austin, TX)
- …pathology and physiology or Business Unit area of expertise + Moderate understanding of medical device regulatory requirements and documents, device ... + Knowledge of cardiovascular physiology and structural heart anatomy + Previous medical device Clinical Research experience in cardiology + Clinical research… more
- Merck (Wilson, NC)
- …risk, generate gap analysis and mitigation strategies + In-depth knowledge of global regulatory requirements for medical devices and combination products and ... Leading International Teams, Management Process, Manufacturing Scale-Up, Medical Device Regulations, Medical Devices , Packaging Engineering, Packaging… more
- Providence (Spokane, WA)
- …team. The Clinic RN maintains compliance with professional nursing standards and regulatory requirements and supports clinicians in delivering quality health care to ... retirement 401(k) Savings Plan with employer matching, health care benefits ( medical , dental, vision), life insurance, disability insurance, time off benefits (paid… more
- Zimmer Biomet (Warsaw, IN)
- …science for application in new product development + FDA QSR and EU MDR medical device regulatory requirements, and industry/ regulatory body recognized ... technical product standards knowledge required; global medical device regulatory requirements knowledge preferred + Demonstrated working knowledge of… more
- Philips (San Diego, CA)
- **Senior/Staff Digital Electrical Engineer** **- FPGA for Medical Devices (San Diego, CA)** As a member of an international cross-functional team, you work ... Biomedical Engineering, or a related field. Experience applying IEC 60601-1 and related medical device electronics standards is desirable. + You must be able… more
- Astrix Technology (Rahway, NJ)
- **Quality Engineer ( Medical Devices )** Engineering Rahway, NJ, NONE Pay Rate Low: 90000 | Pay Rate High: 100000 + Added - 27/08/2025 Apply for Job + **Schedule** ... bonus eligibility Our client, a global leader in the medical device industry, is looking for a...technology solutions for some of the worlds most complex medical devices . **ESSENTIAL DUTIES AND RESPONSIBILITIES:** +… more