- AbbVie (North Chicago, IL)
- …. Job Description This position participates in global regulatory dossier preparation activities by gathering information from internal and external ... (eg third parties) partners and authoring elements of the global dossier . The role prepares technical reports and data-rich sections of regulatory submission… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …an inclusive and collaborative work environment. **Brief Job Overview** The **Senior Manager , Chemical Manufacturing and Controls ( CMC ) Technical Advisor** is a ... to promote engaged, collaborative, and results-driven work environments. **The Senior Manager , Chemical Manufacturing and Controls ( CMC ) Technical Advisor** has… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- The Sr. Manager , CTA Regulatory Strategy is responsible for providing critical support in developing global regulatory strategy , planning, and execution of ... integral member of Otsuka's Regulatory Operations team, provides support for regulatory strategy assignments, monitoring, and oversight, as well as a lead or support… more
- Bausch Health (Bridgewater, NJ)
- …ANDA; BLA; OTC; Devices; Cosmetic; Nutritional). Manages relevant regulatory strategy components and interactions with Regulatory Authorities for these products. ... opportunities. Key Responsibilties: + Responsible for developing a product regulatory strategy for pharmaceutical products + Liaise with regulatory counterparts to… more
- Gilead Sciences, Inc. (Foster City, CA)
- …practices. + Author technical documents such as protocols, reports, regulatory dossier , etc. and prepare data-focused presentations for internal and external ... meetings. + Analyze data and draft conclusions before discussing with manager or supervisor.Support or represent function and work collaboratively on… more