- System One (Alameda, CA)
- …stakeholders. The job scope is focused on authoring and managing the review and approval of moderate to complex CMC regulatory documents, including but ... appropriate CMC-related submissions to health authorities by managing the authoring, review , and approval of regulatory documentation. + Coordinate the development… more
- US Tech Solutions (Newbury Park, CA)
- …Coordinator role provides operational oversight and support for Final Publication Review (FPR) process, ensuring high-quality, compliant delivery of the company's ... role is accountable for processing and tracking FPR submissions, coordinating review and approval workflows, maintaining publication records in Salesforce, and… more
- HCA Healthcare (Austin, TX)
- …in accordance with SDMC Medical Imaging protocols.** + **Administer prescribed pharmaceutical grade radioactive materials to patients as outlined by state/federal ... Nuclear Medicine Technologist** **EDUCATION:** + **Graduate from an approved Joint Review Committee on Education Program in Nuclear Medicine Technology program or… more
- Actalent (St. Louis, MO)
- …Management Systems. + At least 1 year of experience with batch record review and GMP documentation in a pharmaceutical GMP regulated environment. Additional ... prepare logbooks, batch records, and high-risk forms with accuracy. + Perform review processes and assign effective dates to documents. + Manage document-related… more
- HCA Healthcare (Austin, TX)
- …in accordance with SDMC Medical Imaging protocols.** + **Administer prescribed pharmaceutical grade radioactive materials to patients as outlined by state/federal ... Nuclear Medicine Technologist** **EDUCATION:** + **Graduate from an approved Joint Review Committee on Education Program in Nuclear Medicine Technology program or… more
- Actalent (Santa Ana, CA)
- …and Document procedures, including commercial batch record preparation and review . Conducting qualification and validation protocols, as assigned. Assist with ... documenting instrumentation output, interacting with equipment systems, laboratory record review ; and QA support such as non-conformance investigations Skills… more
- CSL Behring (King Of Prussia, PA)
- …Maintain trusted relationships with key thought leaders in relevant fields + Review and approve medical and scientific content of Regulatory, Safety, Scientific ... data gap exercises, evidence generation and publication planning. + Review US promotional material in PRC. + Interact with...US healthcare + 8+ years of experience in the pharmaceutical industry and healthcare. + Prior Medical Affairs experience… more
- Lilly (Indianapolis, IN)
- …for deviations, stability failures and out of specification (OOS) results. Review and approval of the corresponding documentation. + Perform Quality Assurance ... review and/or approval /rejection of GMP documentation and ensure...of 5 years technical and/or quality experience in the pharmaceutical industry, preferred. + Relevant industry experience in highly… more
- Dr. Reddy's Laboratories (Princeton, NJ)
- …for launches and in-line products. + Lead the pricing committee to establish, review and manage the price approval process. + Conduct financial analysis and develop ... content to support the contract review and approval processes including partnership with legal, market...**Minimum experience:** 6 to 8 years of relevant US pharmaceutical experience in any of the following areas -… more
- HonorHealth (AZ)
- …precepting and mentoring of new research staff, and assisting in quality review and process improvement. This position supports our organization's efforts to achieve ... activities such as screening, recruitment, obtaining informed consent, creation and review of source documents, data collection, data entry, query resolution,… more