- Teva Pharmaceuticals (West Chester, PA)
- …new people to make a difference with. **The opportunity** The Director, in Global Regulatory Medical Writing, may write and edit clinical regulatory ... that documents include the proper context and context (from a regulatory medical writing perspective) and clear and consistent medical /scientific messaging,… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …with us. **The Associate Director of Regulatory Affairs** will provide regulatory support for medical device systems within infusion technologies. The role ... of possible** BD is one of the largest global medical technology companies in the world. Advancing the world...Regulatory Affairs. Must have hands-on experience with complex medical device systems and software, specifically Class II or… more
- US Tech Solutions (San Bruno, CA)
- …Quality Concepts (eg, Statistical Analysis, NC/CAPA, Audits) and US and International Medical Device Regulations & Regulatory Agencies (eg, FDA, Notified Bodies, ... and mentoring to engineers to ensure audit readiness and regulatory submissions. + Support bringing novel medical ...and regulatory submissions. + Support bringing novel medical devices from concept to release, manage project schedules,… more
- Teva Pharmaceuticals (West Chester, PA)
- …a difference with. **The opportunity** The Medical Writing Manager in Global Regulatory Medical Writing is responsible for writing and editing clinical ... Manager, Medical Writing (REMOTE) Date: Nov 22, 2025 Location: West Chester,...regulatory documents, providing oversight and guidance, and managing resources for … more
- Actalent (Waukesha, WI)
- …in design and product development of medical devices. + Knowledge of medical device regulatory and safety standards, including ISO, FDA, and IEC60601. + ... within a cross-functional, global project team. + Familiarity with industry design, regulatory , and safety standards. Additional Skills & Qualifications + Master of… more
- Parexel (Jefferson City, MO)
- …full-service and stand-alone projects. **Training/Compliance** + Keep abreast of new advances in medical writing and regulatory issues. + Develop and train ... regulations. + Broad experience in preparation of all types of clinical regulatory documentation. Experience in management of complex medical writing projects.… more
- Lilly (Indianapolis, IN)
- …reimbursement, and access (PRA), grant submissions and contracts; contacts with regulatory and other governmental agencies; the outreach medical activities ... the "patient journey" and the strategic plan for the compound), medical support for regulatory affairs and interactions with government agencies ( medical … more
- American Red Cross (NC)
- …CAR-T support, and emerging therapies.** **Laboratory Compliance** **- Oversee medical and regulatory standards for Cell Therapy Laboratory ... TO KNOW_** You will make an impact as a ** Medical Director** in Transfusion Medicine. In this vital role,...across the organization and beyond. You'll be a key medical leader, shaping policies, guiding clinical services, and fostering… more
- Chiesi (Boston, MA)
- …skills, with the ability to understand and effectively communicate scientific, medical , and regulatory information to internal and external audiences. ... Lead role reports to the Senior Director of Global Medical Affairs HIDO and is part of the Global... Affairs HIDO and is part of the Global Medical Affairs team. This position supports the development and… more
- Trinity Health (Springfield, MA)
- … Medical Staff Coordinator, Credentialist, or similar preferred. Understanding of medical staff regulatory and accreditation standards required. + Experience ... **Employment Type:** Full time **Shift:** Day Shift **Description:** Mercy Medical Center, Springfield, MA Come and join our team of mission-driven healthcare… more