- Fujifilm (Sacramento, CA)
- …II + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and other Key Operators in the use of Fujifilm's Medical Informatics. The Senior Clinical Consultant , MI...business activities. + Adheres to the Company's quality and regulatory compliance requirements and ensures that all job duties… more
- LSI Solutions (Los Angeles, CA)
- …in 1986, located in beautiful Victor, New York, is a dynamic and growing medical device company with over 500 employees dedicated to advancing minimally invasive ... passionate people looking to make a difference in the medical device industry. By joining LSI SOLUTIONS(R)...is ultimately the patient. POSITION TITLE : Surgical Sales Consultant - Los Angeles BASE SALARY RANGE: $50,000.00 -… more
- Norstella (Sacramento, CA)
- …world's leading providers of data and intelligence on clinical trials, drug treatments, medical devices and what's new in the regulatory and commercial ... Senior Solution Consultant Company: Citeline Location: Remote, United States Date...top 10 global pharma and CROs. From drug and device discovery and development to regulatory approval,… more
- Fujifilm (Sacramento, CA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... **Position Overview** The Senior Technical Clinical Consultant , Cardiology shall be responsible for all aspects...+ Ability to work effectively with customers in the medical field. + Ability to prioritize and handle multiple… more
- Cognizant (Sacramento, CA)
- …cross-functional teams developing, and supporting information systems in the Medical Device and pharmaceutical manufacturing industries Understand the ... program Awareness of Electronic Lot History Records using Camstar Software for Medical Device / Pharma industries Implement and execute the shopfloor transaction… more
- Kelly Services (Irvine, CA)
- …* At least 5 years of experience in a Quality, Manufacturing or Engineering function in medical device industry * At least 5 years of experience in a Quality, ... ** REGULATORY COMPLIANCE - SENIOR ANALYST (Hybrid)** QUALIFICATIONS: a)...Manufacturing or Engineering function in medical device industry * Experience with MDSAP… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …with technology solutions that will mitigate risk + Solid understanding of the medical device and healthcare IT space + Advanced analytical and problem-solving ... of possible!** BD is one of the largest global medical technology companies in the world. _Advancing the world...help BUs deliver best-in-class secure products, consistent with global regulatory requirements over the lifecycle. This role works in… 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
- Edwards Lifesciences (Irvine, CA)
- …managing multiple RWE projects concurrently-both internally and with consultants-within the medical device , pharmaceutical, or healthcare industry. + Proficiency ... regulatory and payer landscapes, and evidence requirements for medical devices. + Experience engaging with external stakeholders to support evidence-based… more
- Fujifilm (Sacramento, CA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and competitive positioning to ensure success and become a true "Endoscopic Consultant " for the customer. Has overall responsibility in achieving a 10% annual… more
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