- IQVIA (Raleigh, NC)
- …Our collaborative teams play a vital role in ensuring that biopharmaceuticals, medical devices, patient support services reach those who need them. We offer ... education to patients or prescribers, you can contribute to delivering real-world medical breakthroughs with the right experience. Explore the possibilities and be… more
- United Therapeutics (Research Triangle Park, NC)
- …+ Knowledge of clinical science as applicable to drug development + Medical , scientific, and/or regulatory writing experience + Excellent interpersonal ... We Are** We are the first publicly-traded biotech or pharmaceutical company to take the form of a public...from reviews of the scientific/clinical literature + Collaborate with Medical Science Liaisons and other company staff in identifying… more
- Otsuka America Pharmaceutical Inc. (Raleigh, NC)
- …members of the global regulatory team (GRL, regional leads, CMC-RA, labeling, medical writing , regulatory operations, etc.) to develop global regulatory plans, ... Skills, and Competencies** **K** **nowledge** - Experience working in the pharmaceutical and/or healthcare industry. - Knowledge and experience with preparation of… more
- Lilly (Concord, NC)
- …eligible for remote work) **Additional Skills/Preferences:** + Experience within the pharmaceutical , medical device, or other regulated manufacturing industry ... preferred + Experience as a Quality professional supporting pharmaceutical and/or medical device manufacturing preferred + Knowledge and use of US, EU, Japan and… more
- Merck (Wilson, NC)
- …inspection readiness in areas including manufacturing and packaging production controls, medical device design control and transfer, quality risk management, change ... activities to include quality chapter ownership, defect elimination, procedure writing and development, coordinate deviation response activities. * Assume direct… more
- Otsuka America Pharmaceutical Inc. (Raleigh, NC)
- …and/or clinical pharmacology and associated disciplines (eg biostatistics, data management, medical writing ). + An advanced understanding of clinical medicine ... environment and supports the further development and commercialization of pharmaceutical products, for global launches. This position requires deep understanding… more
- Lilly (Concord, NC)
- …system requirements. Preferred Attributes: + 7+ years in QA roles within the pharmaceutical or medical device industry. + Experience with GMP systems, including ... investigations, including root cause analysis, quality impact evaluations, and technical writing . + Assist and advise deviation reviewers and approvers on issue… more
- Sumitomo Pharma (Raleigh, NC)
- Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... safety report activities including data compilation and analysis as well as writing of assigned sections (with vendor support.) + Compile agenda, data, slides,… more
- Otsuka America Pharmaceutical Inc. (Raleigh, NC)
- …with, and/or be a critical partner to Early Phase & Translational Medical , Clinical Development, Value and Real-World Evidence, Regulatory, Medical Affairs, ... neurology, nephrology or immunology + At least 5 years of experience in pharmaceutical and/or evidence generation and/or digital health in life sciences / technology… more
- Cardinal Health (Raleigh, NC)
- …provides regulatory affairs and product development consulting services to enable pharmaceutical , medical and biotechnology companies to obtain regulatory ... function applies subject matter expertise to provide services in technical writing , scientific data verification, and basic regulatory submissions within the… more
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