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regulatory agency standards. Ensure program is commensurate with services offered. Minimum Qualifications Bachelor's degree in a chemical, physical, or biological science. Five years of relevant experience
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throughout the labeling review and approval process through notification to stakeholders in order to ensure that these documents are produced in a timely manner according to internal SOPs and external
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have the medicines they need, when they need them. What You Will Achieve Working with Pfizer's dynamic engineering team, you will play a critical role in automation development and testing on projects
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to update a CDS/USPI/SPC through notification to stakeholders, in order to ensure that these documents are produced in a timely manner according to internal SOPs and external regulatory requirements
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have the medicines they need, when they need them. What You Will Achieve Working with Pfizer's dynamic engineering team, you will play a critical role in automation development and testing on projects
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order to work with and lead project teams and vendors and to drive the development of high-quality and compliant disclosures. ROLE RESPONSIBILITIES Prepares clinical regulatory documents for public
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information that would attract candidates to the role. It may be helpful to complete this section after you have finished the other sections of the document. The overall role of the Early Clinical Sciences (ECS
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for the Under Secretary for Science and Research. Facilitates communications and works as a liaison between the Under Secretary and other organizations or individuals at SI in order to implement or improve SI pan
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diverse student body; its public mission and commitment to equity and social justice; and its roots in the California experience, animated by such values as innovation, questioning the status quo, and
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Manager is responsible for management of all engineering, functions at the Henkel Salisbury facility. Manages the engineering staff to deliver a safe working environment, processes that result in quality