- Lilly (Lebanon, IN)
- …Lilly Medicine Foundry goes from design, to start-up, and to steady-state operations. The Senior Director , Analytical GMP Laboratories position seeks a ... material release and ongoing process monitoring at the site. The GMP Analytical group will consist of high-level scientists focused on the… more
- Lilly (Lebanon, IN)
- …a successful startup into GMP manufacturing operations._ **Main Purpose and Objectives:** The Senior Director - Quality Control is part of the Senior ... of the Lilly Lebanon API site (LP1). The QC Senior Director provides administrative and technical leadership...the start-up, implementation, and day-to-day operations of LP1. The Sr . Dir. - QC must balance coaching a technical… more
- Lilly (Indianapolis, IN)
- …are determined to make life better for people around the world. Overview: The Senior Director , Global Quality - Supplier and Materials Management, is a member ... Supplier Quality Management partner to Lilly manufacturing networks and sites. The Senior Director collaborates closely with Global Supply Chain, Technical… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. **Position Brand Description:** The Senior Director - QC Labs IPM is responsible for the oversight and ... + Provide technical support and expertise for site and Corporate on analytical topics. + Define and maintain inspection readiness activities; interact with… more
- Lilly (Indianapolis, IN)
- …with expertise in GMP quality assurance and DSCSA compliance. The Sr . Director ensures that DSCSA serialization requirements are met for commercial ... the world. We are seeking a strategic and experienced Senior Director of Drug Supply Chain Security...continuous improvement in quality systems and operational excellence. The Sr . Director - DSCSA Compliance & Manufacturing… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- **Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and ... study protocols and timelines, including sample collection, storage conditions, and analytical testing, to support product development and regulatory submissions. +… more
- Lilly (Indianapolis, IN)
- …of insulins, peptides, oligonucleotides, monoclonal antibodies, and novel gene therapy systems. The Senior Director will be responsible for leading a team of ... rAAV vector production. + Collaborate with cross-functional teams (eg, downstream, analytical , QA/QC, regulatory, and clinical) to ensure seamless integration of… more