- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …selecting appropriate contract testing labs through the Xeris supplier management process * Supporting material qualification processes * Supporting the coordination ... final product through the global supply chain * Managing analytical methods validation and transfer to/from contract testing labs * Overseeing release and stability… more
- Actalent (West Point, PA)
- …work collaboratively in a fast-paced environment to operate LC-MS instrumentation, process data, and summarize results. This role involves solving complex analytical ... toxicity. The scientist will be responsible for the development, validation , implementation, troubleshooting, and transfer of LC-MS methods for...a minimum of 5 years of experience in the Pharmaceutical Industry, or equivalent with a minimum of 8… more
- CBRE (Indianapolis, IN)
- …assist in instrument acquisition, instrument management specific to the pharmaceutical research and development industry. The role also includes responsibility ... etc.). + Performs semi-annual asset inventory. + Computer System Validation . + Assessments - instrument and Documentation + Lead...any use of AI in the application and interview process . Disclaimers: Applicants must be currently authorized to work… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …initiatives to modernize clinical data reporting workflows through standardization, process optimization, and automation to improve programming efficiency and ... the following requirements:** + Demonstrated ability to oversee the development, validation , and delivery of clinical data management programming and visualization… more
- Charles River Laboratories (Mattawan, MI)
- …these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated ... and non-study deviations with minimal oversight * Actively participate in process improvement initiatives with oversight * Develop critical thinking, troubleshooting… more
- Kelly Services (Irvine, CA)
- …pivotal role in ensuring the quality and integrity of our pharmaceutical products through meticulous analytical testing and method development. **Responsibilities** ... + Perform method validation , verification, transfer, and analytical testing for clinical submission...the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource… more
- IQVIA (Durham, NC)
- …to drive quality statistical planning, analysis, and reporting in support of pharmaceutical development and regulatory submissions. Serve as a resource for the ... methodology development work with regards to statistical standards and validation procedures. - Consult on operational/statistical/therapeutic area topics. **Knowledge… more
- Takeda Pharmaceuticals (Brooklyn Park, MN)
- By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... filtration units, chromatography systems and fixed/portable vessels) and will execute validation protocols. You will report to the Manufacturing Supervisor. This is… more
- West Pharmaceutical Services (Scottsdale, AZ)
- …the laboratory team in the areas of test method development & validation , equipment management, device testing, and data analysis. Responsible for the management ... and engaging key stakeholders and cross-functional resources throughout the process . **Essential Duties and Responsibilities** + Direct management over the… more
- Eurofins US Network (West Point, PA)
- …standards in laboratory operations. + Assist with computer system and instrument validation process for diverse laboratory equipment such as automated liquid ... is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is… more