- Otsuka America Pharmaceutical Inc. (Baton Rouge, LA)
- …development programs. + Build professional network with key stakeholders outside of Global Regulatory Affairs to identify regulatory intelligence needs and ... a scientific or technical discipline preferred. + Minimum of 5 years of regulatory affairs experience. + Minimum 2-3 years' work experience in regulatory … more
- Reckitt (Evansville, IN)
- …Infant Formula, and how regulations may impact work assignments. + Reviews Regulatory Affairs standard operating procedures and work instructions as needed. ... This role also offers great promotion opportunities, with a Senior Manager position being the next step for strong...+ At least 5 years of work experience in Regulatory Affairs / food industry. + Demonstrated… more
- BeOne Medicines (San Mateo, CA)
- …are met while leveraging expedited pathways where appropriate. The individual has regulatory affairs departmental and cross functional influence and acts as ... working experience. + Preferred candidates will have experience working as a lead in Regulatory Affairs across two or more major geographic areas, and prior… more
- Otsuka America Pharmaceutical Inc. (San Juan, PR)
- …external engagement across therapeutic areas + Collaborate with global and US Medical Affairs teams to ensure alignment with scientific and commercial priorities ... The Senior Manager, External Engagement Strategic Planning will play...executing strategic initiatives that enhance the impact of Medical Affairs external stakeholder engagement activities (including those of the… more
- Abbott (Santa Clara, CA)
- …device regulations and guidelines, and product and therapeutic area knowledge to support Regulatory Affairs medical device submissions in the EU for CE Marking ... and exchange of documents between stakeholders (eg, internal personnel such as Regulatory Affairs , R&D Engineering, Clinical Engineering, A&P and Marketing,… more
- Bristol Myers Squibb (Brisbane, CA)
- …TM, clinical pharmacology, toxicology, regulatory , HEOR, market access, medical affairs ), applying foresight, scientific and development knowledge to ensure ... than 5 years of extensive clinical trial and drug development experience and regulatory experience, in addition to a strong scientific background, particularly… more
- J&J Family of Companies (Titusville, NJ)
- …Device Development and Regulation, Program Management, Regulatory Affairs Management, Relationship Building, Safety-Oriented, Scientific Research, Strategic ... via matrix interactions includes individuals from TA strategy, GCSO, global regulatory affairs , project management, finance, legal, quality assurance, quality… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …or equivalent and, 8 years direct experience in Medical Research, Clinical, Regulatory Affairs or other critical areas within the pharmaceutical industry. ... training, reviews and development of department members. + Advises Senior Management on regulatory aspects of product...resources and budget to meet R&D goals + Utilizes scientific training when interfacing with Senior Management… more
- AbbVie (North Chicago, IL)
- …of an overall Product Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's ... generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business strategy. Responsibilities: + Manages the design and… more
- Merck (Boston, MA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Senior Director May… more