- Bio-Techne (San Marcos, CA)
- …Food and Drug Administration (FDA) and industry standards. . Participate in management review meetings and/or prepare information and trending data to be shared ... including new products, Supplier Corrective Action Reports, change notifications, etc. Review SCARs sent back from suppliers to assess corrective actions. Conduct… more
- US Tech Solutions (New Albany, OH)
- …to sampling raw materials, labels, and sanitary utilities, and generating/compiling quality data and reports (eg lot track/trace, incidents). Will also assist with ... document review and initiate incidents, as well as coordinate and...Skills: ; quality assurance or manufacturing experience in the pharmaceutical or medical device industry **Key Responsibilities:** + Provide… more
- Lilly (Indianapolis, IN)
- …Systems to sustain cGMP compliance. + Ensure adequate document control and data integrity for packaging instructions and cGMP standards. + Review /approve/release ... Analysis. + Provide quality support for packaging operation. + Investigate, review /approve deviation investigations. + Review /approve change controls, protocols… more
- Mount Sinai Health System (New York, NY)
- …reports as requested for departments and individual researchers + Grants Specialist Review approximately one thousand grant applications per year for all pre-award ... and routing to the Institutional Animal Care and Use Committee, Institutional Review Board, Bio-Safety Officer and Financial Conflict of Interest in Research… more
- Rush University Medical Center (Chicago, IL)
- …experience and skills, as well as internal equity and industry specific market data . The pay range for each role reflects Rush's anticipated wage or salary ... responsible for assuring the effective and efficient provision of pharmaceutical care services. Perform all duties necessary to provide...be performed on new orders or as a profile review of a target patient population. 4. A profile… more
- GRAIL (Menlo Park, CA)
- …sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome one of medicine's greatest challenges. GRAIL ... United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com… more
- Bristol Myers Squibb (Princeton, NJ)
- …degree preferred (MS, PhD, PharmD, JD) + Minimum of 3-5 years Regulatory promotional review or related 5 to 8 years pharmaceutical experience (eg, Medical ... campaigns + Proven aptitude to analyze and interpret efficacy and safety data + Experience communicating and negotiating with OPDP + Organizational skills and… more
- Sanofi Group (Framingham, MA)
- …The team develops and implements global regulatory strategies for pharmaceutical products, biologics, vaccines, and combination products, working closely with ... Authorities **Manage CMC documentation and submissions** + Write, prepare, review , and approve regulatory CMC dossiers + Ensure dossiers...or interest on using IA to produce information or data intended to support CMC filings + RAC certification… more
- State of Colorado (Aurora, CO)
- …Job As a Pharmacy Technician, you will perform day-to-day professional pharmaceutical operations of the department, which includes drug acquisition, distribution, ... Prices prescriptions, inputs resident information into the computer. Resident data includes such data as resident name,...appeal with the State Personnel Board or request a review by the State Personnel Director. An appeal or… more
- Pfizer (Bothell, WA)
- …of diverse scope requiring skilled analysis of the situation and/or data + Facilitate stakeholder to prioritize initiatives, balancing fiscal responsibility and ... control records for document and/or equipment changes. + Perform data integrity and impact assessments for equipment and associated...equipment and software periodic reviews + Create new and review completed equipment records and tasks in the CMMS… more