- Sanofi Group (Cambridge, MA)
- …responsibilities. **About You** **Experience:** + 8+ years of experience within pharmaceutical or medical device Regulatory Affairs + Successful track record ... **Job Title:** Director, US Regulatory Affairs - Advertising and Promotion **Location:** Cambridge,...+ Dealt effectively with cross-functional groups, which may include Medical , Legal, Marketing, etc. + Experience managing others is… more
- Bayer (Indianola, PA)
- …ensure registration of products; + Support international registrations within the Radiology Medical Device Regulatory Affairs group; + Maintain registration ... minds to make a real difference, there's only one choice.** ** Regulatory Specialist Co-Op** **YOUR TASKS AND RESPONSIBILITIES** The primary responsibilities of… more
- Fujifilm (Jackson, MS)
- …to Division General Counsel and senior business management on general legal and regulatory risks affecting the Medical Device businesses, including with ... part of the legal team providing support to the Medical Device businesses of FUJIFILM Healthcare Americas...The Senior Counsel, reporting to the Division General Counsel, Medical Devices , will be an experienced commercial… more
- Jabil (West Chester, PA)
- …and foster vibrant and diverse communities around the globe. Are you experienced in Medical Device Regulatory Compliance? Jabil is seeking a qualified ... Quality Systems & Compliance Lead for Medical Device to work in our West..., you will manage, as an individual contributor, all Regulatory Compliance activities at the assigned sites. You will… more
- Lilly (Indianapolis, IN)
- …Unit Leadership + Regulatory (including Device and CMC regulatory ) + Affiliate Medical Leadership/Clinical Research Physicians + COE and Discovery ... for people around the world. **Clinical Research Physician, GPS Medical ** **Purpose:** The Clinical Research Physician (CRP) in GPS...+ Responsible for the oversight and actions related to regulatory queries on safety-related topics + Acts as the… more
- Sanofi Group (Morristown, NJ)
- …(early phase, late stage and marketed products). + Develop innovative and sustainable medical device regulatory strategies covering combination products and ... to internal regulatory processes and procedures for medical devices and combination products. + Engage...regulatory experience. At least 5 years of relevant medical device and/or combination product regulatory… more
- Fresenius Medical Center (Waltham, MA)
- …issues and broad design matters. + Understands and interprets US and international medical device regulatory requirements, provides guidance on requirements ... lines. Prepares regulatory submissions required to market new or modified medical devices in the domestic and international clinical markets. Develops and… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …of five (5) years of Regulatory Affairs experience in the medical device industry required + Strong prioritizing, interpersonal, communication, and ... crucial role in supporting Medication Management Solutions (MMS) dispensing products, including non- medical devices , medical devices , associated… more
- US Tech Solutions (San Bruno, CA)
- …of Quality Concepts (eg, Statistical Analysis, NC/CAPA, Audits) and US and International Medical Device Regulations & Regulatory Agencies (eg, FDA, Notified ... + Managing cross-functional or cross-team projects to bring regulated medical device products to market. + Ensuring...and regulatory submissions. + Support bringing novel medical devices from concept to release, manage… more
- Abbott (Plymouth, MN)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... to various international affiliates. + Maintains pertinent domestic and international medical device regulations to ensure submission requirements world-wide are… more