Demonstrated ability to lead the development, review, and approval of all clinical regulatory document types (ie, those typically developed by CSW) and the ability to develop new or unique document types.
May 09, 2020
Provide technical support to department where required to ascertain degradation profiles, solve complex scientific problems and develop sophisticated analytical methods.
June 26, 2020
Required two (2) years experience in job offered, Software Consultant, IT Engineer, or related using MDM (Master Data Management), MRP (Material Requirement Planning), and Quality Management.
July 08, 2020
Prepares oral and written reports to effectively communicate results of clinical studies to project team, management, regulatory agencies, or individual investigators.
July 25, 2020
Lead and manage project teams in the delivery of cross-functional projects across multiple areas of expertise, including product commercialization and launch, portfolio and product strategy, and organizational strategy and excellence.
August 10, 2020
Design of testing methodologies for Client AccelerateNOW tool's re-designed functionality in the United States, including the design and implementation of User Acceptance Testing.
August 13, 2020
Evaluates appropriateness of available software for planned analyses and ascertains needs for potential program development for implementation of novel statistical methodology.
August 18, 2020
Acts as a subject matter expert to effectively partner with EP2 to achieve desired outcome or improvement by clarifying needs and providing appropriate solutions.
August 21, 2020
Build successful relationships with line of business risk offices and Cyber Security partners to understand the impact of technology risk on critical business processes.
August 30, 2020
Develop toxicological risk assessments in support of all commercial activities to ensure internal food safety programs receive the most up-to-date and science based advice.
October 05, 2020