- Abbott (San Diego, CA)
- …team, reporting to the Director of Global NPI and US Regulatory Affairs . We're empowering smarter medical and economic decision-making to help transform the ... in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs , operations, or related area. + Note: Higher… more
- Chiesi (Boston, MA)
- …goals. Experience Required + Required Skills: + * 10+ years of experience in medical affairs , scientific communications, medical information, or ... Who we are looking for Purpose As the Senior Director , Global Scientific Engagement and Innovation, you...data security) to ensure Chiesi becomes a trailblazer in medical affairs through 2030. + Lead a… more
- J&J Family of Companies (Titusville, NJ)
- …and maintenance of customer-facing materials + Collaborate regularly across Scientific Affairs , Strategic Customer Group (SCG), Medical Affairs , Research ... , Strategic Communications & Learning (SC&L), part of the Scientific Affairs (SA) Value & Evidence ... field is preferred **Professional Experience:** + 3-5 years medical communications, writing, medical information, scientific… more
- Abbott (Alameda, CA)
- …diversity, working mothers, female executives, and scientists. **The Opportunity** This **Associate Director Regulatory Affairs - APAC** will work on-site at our ... Division. As a manager, the function of an Associate Director Regulatory Affairs , APAC (Asia Pacific) is...or MBA + Minimum 5+ years' experience in regulatory affairs . + Experience working with Medical Devices,… more
- Takeda Pharmaceuticals (Boston, MA)
- …life-changing therapies to patients worldwide. The Senior Global Regulatory Affairs , Neuroscience is responsible for developing innovative global regulatory ... the regulatory function on cross-functional Global Program Teams. The Senior Director also will lead discussions of regulatory strategy with senior leadership… more
- Takeda Pharmaceuticals (Boston, MA)
- …in collaboration with their regional counterparts. **Accountabilities:** + The Associate Director will be responsible for complex or highly complex or multiple ... approvals of project(s) of responsibility or oversees direct reports responsible. The Director will lead all submission types. + Accountable for building global… more
- Lilly (Indianapolis, IN)
- …determined to make life better for people around the world. **Purpose:** The Senior Director of Global Regulatory Affairs - CMC (GRA-CMC) leads and manages the ... synthetic molecule portfolio. This role ensures the integration of robust scientific principles into regulatory strategies for both development and commercial… more
- J&J Family of Companies (Horsham, PA)
- …Johnson & Johnson Innovative Medicine R&D is recruiting for a Director , CMC (Chemistry, Manufacturing and Controls) Regulatory Affairs Biologics ... be located in Horsham, PA; Spring House, PA; Titusville, NJ; or Raritan, NJ. The Director , CMC Regulatory Affairs Biologics New Modalities will lead a team of… more
- Ascendis Pharma (Palo Alto, CA)
- …a dynamic workplace for employees to grow and develop their skills. The Director , Regulatory Affairs will be responsible for developing and implementing global ... mission of developing new and potentially best-in-class therapies to address unmet medical needs. Our culture fosters a place where skilled, adaptable, and highly… more
- Gilead Sciences, Inc. (Foster City, CA)
- …inflammation, and serious respiratory and cardiovascular conditions. **KEY RESPONSIBILITIES** The Director , CMC Regulatory Affairs for Biologics is responsible ... team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve… more