- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …in pharmaceutical quality , with 2+ years in supplier or external manufacturing quality . + Strong knowledge of GMP regulations for small molecules and/or ... The Associate Director of Global Supplier Quality will be responsible for the execution of... will be responsible for the execution of supplier quality audit and monitoring across the company's global network… more
- Mondelez International (Indianapolis, IN)
- …scientific thinking to the resolution of problems. . Working knowledge of HACCP, GMP 's, and quality systems in a food manufacturing environment. . Proficient ... You lead the plan-do-check-act (PDCA) process of the site quality management system and report results to the ...quality management system and report results to the quality section manager. **How you will contribute** You will… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …knowledge of drug development process, pharmaceutical technology, drug manufacturing processes, analytical/ quality control, GMP and related issues. + Knowledge ... as CMC regulatory lead on global project teams (Pharmaceutical Development, Quality , Manufacturing, Global Regulatory Strategy). + Assess and provide regulatory… more
- Bristol Myers Squibb (Indianapolis, IN)
- … GMP spaces including but not limited to office, warehouse, development, quality control, sterility/microbiology, and GMP production areas. * Work with ... The Validation Engineer II will help support the Radiopharmaceutical facility and GMP operations in Indianapolis. The Validation Engineer II will be responsible for… more
- Bristol Myers Squibb (Indianapolis, IN)
- …processes. * Lead the strategy and implementation of CQV programs for GMP spaces: office, warehouse, development, quality control, sterility/microbiology, and ... Engineer will lead validation efforts to support the Radiopharmaceutical facility and GMP operations in Indianapolis. This role is responsible for the development,… more
- Lilly (Indianapolis, IN)
- …due diligence project and coordinate completion and networking of all GCP, GLP and GMP reports to quality management and others as appropriate, including a ... and speed. By shaping the selection and adoption of quality oversight models, GQAAC ensures that innovation is built...development due diligence activity to include GCP, GLP and GMP as appropriate. This may also include working outside… more
- System One (Indianapolis, IN)
- …provide a globally holistic process in which GMP supplier and GMP service provider's Supplier Quality Management activities are globally consistent, ... + Provide support to ensure maintenance of the supplier quality management data, including approved supplier and GMP... quality management data, including approved supplier and GMP service provider list, in the appropriate systems, eg,… more
- Nestle (Anderson, IN)
- …+ Prepare paperwork / reports on a timely basis. + Follow all sanitation, GMP , safety, quality and employee relation programs. + Confirm processes are run ... or area. You focus on improving safety, reducing costs, enhancing quality , and maximizing effectiveness through long-term planning and project implementation. You… more
- Lilly (Indianapolis, IN)
- …+ Direct or indirect experience with commercialization (Validation, Tech Transfer, CMC, GMP , Quality , and/or HSE) + Demonstrated ability to function in ... manufactured APIs, intermediates and starting materials with safety first and quality always. The role reflects increasing technical complexity and commercialization… more
- Lilly (Indianapolis, IN)
- …Foundry, including benchmarking with other Lilly sites. + Evaluate potential product quality impact for any GMP -related incident (deviation or change control), ... and computer systems (CSQ) within the Foundry and assures compliance with quality systems and current Good Manufacturing Practices (cGMP). This oversight includes… more