- Teva Pharmaceuticals (Parsippany, NJ)
- …trends, cost drivers along with business understanding of the overall pharmaceutical industry and related regulations. Understanding of other supply markets would ... be required to analyze business requirements, as part of global category management team, create multi-year category strategies, drive and implement sourcing plans… more
- Adecco US, Inc. (Clark, NJ)
- …company in New Jersey. This role supports regulatory compliance and product management within the cosmetics or pharmaceutical industry. Responsibilities may ... include: **Pay** : Up to $29.4/hr depending on experience level + Reviewing raw materials and formulas for regulatory compliance. + Monitoring and tracking changes in global regulations. + Supporting product notifications, registrations, and submissions. +… more
- Cardinal Health (Trenton, NJ)
- …improvement of Operations strategy by leveraging expertise in the specialty pharmaceutical market and GPO operations. + Support cross-functional teams to refine ... solutions for Wholesaler Contract Load, Contract Alignment, and Membership Management (including roster management , manufacturer notifications, participant… more
- Taiho Oncology (Princeton, NJ)
- …and Abilities: + 2 years of relevant clinical trial support or site management experience in the pharmaceutical , biotechnology, CRO and/or healthcare industry. + ... Experience and knowledge of Trial Master File and essential documents. + Has demonstrated the use of excellent communication skills, command of medical terminology and of the application of scientific/medical and clinical concepts used to conduct clinical… more
- Sanofi Group (Morristown, NJ)
- …systems **About you** + 5+ years' experience working in life sciences or pharmaceutical R&D, especially in technical product management or scientific computing + ... Proven success delivering data visualization or analytics products in a research environment + Global stakeholder manager, collaboration and facilitation skills + Strong understanding of scientific data types (eg, omics, imaging, molecular, clinical) and… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …manner to meet required timelines. + Develop clear communications for senior management and SOP approvers to streamline and facilitate final label negotiations and ... (MSc, PhD or PharmD) preferred. + 10+ years of relevant pharmaceutical Labeling/Regulatory experience. + Thorough understanding of scientific principals and… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …teams: Strategic Planning, Business Solutions & Analytics, Vendor & Contracts Management , Governance & Procedures, and Global Medical Evidence Operations ensuring ... of strategic and tactical planning and execution. **Operational Excellence and Team Management ** + Lead and manage core operational pillars within Medical Affairs… more
- ThermoFisher Scientific (Cranbury, NJ)
- …and emerging industry developments that directly influence our business in pharmaceutical product development. Applying your expertise, you will actively contribute ... of relevant global regulations, guidelines, and evolving regulatory trends relating to pharmaceutical product development in the area of cell and gene therapy. +… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …experience in regulatory affairs or related areas (eg, clinical development, project management , quality assurance, etc.) in pharmaceutical or healthcare related ... Skills, and Competencies** **K** **nowledge** - Experience working in the pharmaceutical and/or healthcare industry. - Knowledge and experience with preparation of… more
- Hovione (East Windsor, NJ)
- …as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off-patent drugs to market. Our people ... facilities under responsibility. Propose necessary investments. Support manufacture of pharmaceutical products (Active Pharmaceuticals Ingredient, Drug Product Intermediates and… more