- Fujifilm (Boston, MA)
- …I. + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... **Position Overview** The Senior Clinical Consultant , MI - II International has advanced technical/Clinical...and other Key Operators in the use of Fujifilm's Medical Informatics. The resource will assist with the development… more
- Norstella (Boston, MA)
- …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 (Boston, MA)
- …+ 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
- SHI (Boston, MA)
- …**Job Summary** The Information Technology Spend Optimization (ITSO) Procurement Consultant is responsible for helping customers achieve cost savings through ... teams to ensure that all procurement activities adhere to legal and regulatory requirements. + Prepare, review, and revise customer contract templates, ensuring… more
- Cognizant (Boston, MA)
- …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
- Chemours (Boston, MA)
- …Engineering, Biological Science, Toxicology or comparable technical field + 5+ years of medical device regulatory compliance experience with respect to raw ... outside lawyers, consultants, industry associations, and local agencies on specific medical regulatory topics. + Coordinate and review customer… more
- Abbott (Burlington, MA)
- …various types of product complaints. Independently assesses the complaint to determine if a medical device report needs to be filed with various global ... + 5 years related work experience **Preferred Qualifications** + 3+ years in MDR ( Medical Device Reporting) + Knowledge of the use, development, and … more
- Abbott (Boston, MA)
- …Experience** + Associate's degree required + 7 years of Cath Lab and/or Medical Device experience **Preferred Experience** + Bachelor's Degree highly preferred. ... and provides reporting information for reports submitted to the regulatory agencies. * Monitors adherence to protocols and determines...Development + Cath Lab Tech or Surgical Tech + Medical Device experience + OCT experience Please… more
- ConvaTec (Lexington, MA)
- …human-centered innovation to improve people's lives with deeply personal and challenging medical conditions. And this is where you come into the picture; We ... about bringing the user's perspective into the development of medical devices and is unafraid to make things happen...of the process from the very beginning, through the device development, to launch - and beyond. Main responsibilities… more
- Fujifilm (Boston, MA)
- …+ 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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