- Novo Nordisk Inc. (Durham, NC)
- … quality processes are compliant with regulations Authority for product release Quality oversight, review & approval of validation activities associated with ... life-changing careers, and the opportunity to help improve the quality of life for millions of people around the...handled in close collaboration with production. Main duties include review of batch reports & release of incoming materials,… more
- Novo Nordisk Inc. (Boston, MA)
- …as a frontrunner in the cardiometabolic care market. The Ecosystem Portfolio Specialist is responsible for achieving sales targets by effectively promoting Novo ... adherence to approved guidelines. Relationships Externally, the Ecosystem Portfolio Specialist maintains relationships with physicians, pharmacists, nurses, and other… more
- Novo Nordisk Inc. (Boulder, CO)
- …us. Our R&D hub merges biotech speed and agility with large pharmaceutical company quality , resources, and stability, uniting the best of both worlds to develop new ... medicines for patients. The Position The Specialist , Logistics & Global Trade Compliance is responsible for...action when there are issues with non-compliance Conducts monthly review of exports reported through AES to ensure accuracy… more
- Merck & Co. (South San Francisco, CA)
- …focused on bringing AI/ML approaches to bear to improve the speed and quality of decision-making in drug discovery and development. PDMB aims to leverage Generative ... implementing, and optimizing GenAI approaches to streamline the creation and quality control (QC) of regulatory submission documents. The candidate will be… more
- Novo Nordisk Inc. (Durham, NC)
- …(CR's) related to revalidation & other validation activities for AP Author & review validation procedures, specifications & quality documents for accuracy & ... in pharmaceutical or medical device industry required Experience in quality concepts including technical & compliance review ...in quality concepts including technical & compliance review of validation & quality documents required… more
- Merck & Co. (Rahway, NJ)
- …supplies.-Interacts with key partner organizations such as clinical development, regulatory, quality and other supply chain areas to address clinical supply related ... chain deliverables and prepares, analyses, and/or develops mitigation strategies for review with clinical partners and senior leaders.--Works directly in the SAP… more
- Merck & Co. (Rahway, NJ)
- …Clinical Trial Operations (GCTO) Regional colleagues and Global Development Quality (GDQ) to address clinical supply related topics.-Responsible and accountable ... deliverables and prepares, analyzes, and/or develops mitigation strategies for review with clinical partners and senior leaders.--Responsible and accountable for… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …and execution of process and equipment improvement initiatives, reviews completed quality records, generates quality deviation responses, drive investigations ... for the coordination of process/equipment improvements and data trending/analysis Review /approval of completed process documentation Ability to train others on… more
- Merck & Co. (Lower Gwynedd, PA)
- …pipette calibration, maintaining records in the electronic logbook. Generate and review out-of-calibration impacts reports, share it with management and take ... a bioanalytical setting.Proven experience in validation activities and associated Quality functions.Demonstrated strong interpersonal skills with the ability to… more
- Novo Nordisk Inc. (Fort Smith, AR)
- …audience needs, share learning objectives and local challenges, provide feedback on quality of presentation) to provide quality balanced and relevant ... by not exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records. Qualifications Bachelor's or equivalent degree, and/or Pharm… more
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