- Lilly (Indianapolis, IN)
- …for people around the world. Join the energetic and growing Active Pharmaceutical Ingredient - External Manufacturing Organization (API-EM) that delivers a diverse ... and approve quality-related documents, such as manufacturing master batch records, validation protocols and reports, stability data, and analytical methods. +… more
- CBRE (Indianapolis, IN)
- …site. The Project Management Team supports project delivery at a major pharmaceutical company. The primary responsibility of the Program Management Principal is to ... activities may include a combination of Commissioning, Qualification, and/or Validation for facilities, equipment, and computerized systems. Implement projects while… more
- Lilly (Indianapolis, IN)
- …and mentor PhD and non-PhD scientists engaged in target identification, validation and preclinical drug discovery + Supervise laboratories. Ensure adherence to ... for novel small and large molecule target discovery and validation + Coach team members to think deeply and...10 years of experience in drug discovery in the pharmaceutical industry. + Thorough understanding of drug discovery and… more
- Lilly (Indianapolis, IN)
- …engineering associates in aspects of fundamental engineering support, including process knowledge, problem solving and engineering design + Provide administrative ... oversight and support to a team of process engineers across multiple geographies + Develop and provide ongoing leadership for a PSM program within API EM with the… more
- Lilly (Indianapolis, IN)
- …systems/technology projects. + Demonstrates understanding of the PV safety system and business process . + Experience in the pharmaceutical industry and/or PV or ... improvement opportunities, efficiency enhancements, and increased quality of data and process . They will use their business process analysis, benchmarking,… more
- Nestle (Anderson, IN)
- …In Touch and Middleware, * Awareness of FDA & GMP/GAMP regulation and validation in the pharmaceutical or food industry. \#LI-JM1 \#AndersonSalary It is ... * Participate in competency assessments and identify areas for improvement. Support Process Improvements: * Gain a thorough understanding of processes and provide… more
- Lilly (Indianapolis, IN)
- …including risk assessments and documenting and maintaining the state of process /sterility assurance/cleaning validation . **Key Objectives / Deliverables:** + ... governance to the technical/scientific agenda for the site via the Science Lead Team ( process monitoring) + Represent the TS/MS organization at the Site Lead Team +… more
- Bristol Myers Squibb (Indianapolis, IN)
- …the following. Other duties may be assigned. + Support Quality disposition process by ensuring that all required documents are accurately and properly completed ... with and provide QA approval of investigations, CAPAs, change controls, validation documentation, and other related GMP documentation related to Externally… more
- Lilly (Indianapolis, IN)
- …execution of clinical protocol(s) / programs (including interventional, non-interventional, validation , natural history, and registry trials / studies) + Supports ... the Life Sciences required. + A minimum of ten (10) years of pharmaceutical and/or clinical experience **Additional Skills / Preferences:** + Prior pharma/biotech or… more
- Parkview Health (Fort Wayne, IN)
- …conflict management, willing to actively learn new concepts, and able to deconstruct a process to drive improvement. They will thrive in a culture where success of ... variety of areas for decades. Parkview offers a progressive pharmaceutical care environment in a variety of practice settings,...Work in Healthcare in April 2024. + Stage 7 Validation awards from the Healthcare Information and Management Systems… more
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