- Lilly (Lebanon, IN)
- …Lilly Medicine Foundry, a new center for advanced manufacturing and drug development . The first-ever facility of its kind, combining research and manufacturing in ... design, to start-up, and to steady-state operations. The Laboratory Informatics Director role, a technical-track position, seeks a collaborative, inclusive, and… more
- Bristol Myers Squibb (Indianapolis, IN)
- …procurement, installation, commissioning, cost forecasting and validation of facility and various process technologies. As a people leader, the Director fosters ... RayzeBio aims to be the global leader in radiopharmaceuticals. **Summary** The Director of Capital Project Engineering is responsible for the successful management… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …processing. + Collaborate closely with Upstream MSAT, Validation MSAT, QA, Regulatory, Process Development , Analytical Development , and CDMO technical teams. ... biopharmaceutical industry with a strong focus on biologics downstream process development , scale-up, technology transfer, and/or manufacturing sciences/support.… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …including cell culture, purification, and formulation + Proven track record in process development , scale-up, and technology transfer of biologics products + ... **Position Overview:** The Senior Director , MSAT Biologics provides strategic and technical leadership for all late-stage and commercial manufacturing processes for… more
- Lilly (Indianapolis, IN)
- …is responsible for the oversight and execution of the product testing; including Chemical and/or Micro tests for raw materials, in- process samples, semi-finished ... the adequate resourcing of the quality control unit and the continuous professional development of the quality control team. This position requires the ability to… more
- Lilly (Indianapolis, IN)
- …or manufacturing. + Demonstrated deep knowledge of the synthetic molecule drug development process . Knowledge in new molecular modalities (eg, oligonucleotides, ... medicines to patients who need them all over the world. The Senior Advisor/ Director in Global Regulatory Affairs - CMC Pre-approval Small Molecules will leverage CMC… more
- Mitsubishi Chemical Group (Indianapolis, IN)
- …(edaravone) oral suspension in 2022. The company handles research, clinical development , sales, marketing, medical affairs, supply chain,and business development ... real-world evidence, and creating hope for all facing illness. The Regional Business Director (RBD) will be responsible for building and leading a team of Neurology… more
- Lilly (Indianapolis, IN)
- …position responsibility is to address and document GMP compliance issues and development /execution of process /cleaning validation plans. Therefore, the ... better for people around the world. **Summary:** The Associate Director - TS /MS - IAPI is primarily responsible...- IAPI is primarily responsible for the productivity and development of the employees with the purpose of ensuring… more
- Lilly (Indianapolis, IN)
- …and manages external teams from multiple companies. Responsibilities for a Director -level DVL (Design Verification Lead) include: + Overall design delivery for ... design review and basic design review. + Direct the development of the design requirements. + Command of the...to resolve problems. Basic Qualifications: + BS in Engineering ( Chemical or Mechanical strongly preferred) + Minimum of 15… more
- Lilly (Indianapolis, IN)
- …medicines to patients who need them all over the world. The Senior Advisor/ Director Post approval scientist in Global Regulatory Affairs - CMC commercial solid oral ... completion of submission milestones leading to health authoring approval. + Development of regulatory strategy and update strategy based upon global regulatory… more