- Otsuka America Pharmaceutical Inc. (Jefferson City, MO)
- **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial ... integrity while optimizing operational efficiency. + Works collaboratively within the Global Quality Dept. and other functions within OAPI and OPDC to assure… more
- Otsuka America Pharmaceutical Inc. (Jefferson City, MO)
- The Associate Director of Global Supplier Quality will be responsible for the execution of supplier quality audit and monitoring across the company's ... monitoring, and compliance of external manufacturing partners to ensure the quality and reliability of pharmaceutical products, including small molecules and… more
- Otsuka America Pharmaceutical Inc. (Jefferson City, MO)
- **Job Summary** The Associate Director Controlled Substances, Quality Global Product Quality - API/DP is responsible for directing quality ... final finished product) for controlled substances + Works collaboratively within the Global Quality Dept. and other functions within OAPI and OPDC to assure… more
- Otsuka America Pharmaceutical Inc. (Jefferson City, MO)
- **Job Summary** The Associate Director , Quality Operations will lead initiatives that drive operational excellence, enhance risk management practices, and ... optimize global quality system processes across a global quality organization. This role is instrumental in ensuring that quality operations are… more
- Otsuka America Pharmaceutical Inc. (Jefferson City, MO)
- **Summary:** The Global Integrated Evidence Operations, Associate Director role oversees and coordinates the operational processes, digital system support, ... and governance for Global Integrated Evidence & Innovation (GIE&I), which includes responsibility for operating models, system readiness, and process adherence for… more
- Otsuka America Pharmaceutical Inc. (Jefferson City, MO)
- …negotiations, and approval. + Review and propose continuous improvements to Global Labeling policies, end-to-end processes, quality , and system tools. ... across the organization to drive and align the development and maintenance of global labeling (eg CCDS, regional product labels, and patient labeling) for assigned… more
- Wolters Kluwer (Clayton, MO)
- **Software Quality Assurance - Associate Director - Hybrid USA** **R0051123** **| DXG | FCC CS Software Development | Wolters Kluwer** **About the Role** As ... the **Software Quality Assurance - Associate Director **...available - https://www.mywolterskluwerbenefits.com/index.html Wolters Kluwer (EURONEXT: WKL) is a global leader in professional information, software solutions, and services… more
- Otsuka America Pharmaceutical Inc. (Jefferson City, MO)
- The Associate Director , Scientific Communications manages the execution of the core scientific and medical communications strategy for the relevant therapeutic ... Director , CNS Medical Communications Lead. **Key Responsibilities Include:** ** Global Scientific Communication Strategy** + Manage and deliver a comprehensive,… more
- Boehringer Ingelheim (St. Joseph, MO)
- …such as governance review, project team meetings, planning activities and FDA communications. Associate Director Act as Regulatory Affairs (RA) core or subteam ... of regulatory tools as defined. + Supports specific infrastructural projects as assigned. Associate Director + Responsibility for the safety and efficacy part of… more
- Sumitomo Pharma (Jefferson City, MO)
- …of ** Associate Director , Regulatory Affairs (Oncology).** The Associate Director is part of the Global Regulatory Affairs (GRA) team based in the ... Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations...provides possible solutions and mitigation strategy + Ensures the quality and content of all submissions to Health Authorities… more
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