- Lilly (Indianapolis, IN)
- …products, through effective quality oversight of Indianapolis Parenteral Manufacturing's central quality processes. The Associate Director for Site ... for complaint investigation management and oversight of the IPM GMP Library within the Site Quality &... & Compliance team. Cross-training to back-up other Site Quality and Compliance Associate Directors is expected.… more
- Lilly (Lebanon, IN)
- …to enable a successful startup into GMP manufacturing operations._ **Responsibilities** The Associate Director - Head of TS/MS Lab will lead a technically ... development. In this role you will work collaboratively with peers in the quality control laboratory, engineering, development and quality assurance. + Assisting… more
- Lilly (Indianapolis, IN)
- … Analytical Sciences & QC Operations (AQCO) team is also growing. The Associate Director , Analytical & QC Integrated Services (AQIS), will provide leadership ... provides QA Oversight, and QC Compendial Affairs support to the organization. The Associate Director is accountable for the successful operation of the internal… more
- Lilly (Indianapolis, IN)
- …products in vial, cartridge, and pre-filled syringe formats with Safety First and Quality Always. The Associate Director - Engineering sets strategies ... using some of the most sophisticated manufacturing technologies and rigorous quality standards. Lilly Manufacturing strives for excellence in its process, standards,… more
- Lilly (Indianapolis, IN)
- …lead the charge in shaping the future of manufacturing at Eli Lilly? As an Associate Director of Engineering, you'll be at the forefront of this exciting ... leaders, you'll influence and implement our organizational agenda, business priorities, and quality objectives to drive success down to the floor level. **Key… more
- Lilly (Lebanon, IN)
- …prevent and mitigate variability to deliver a reliable supply of medicine. The Associate Director is primarily responsible to lead TS/MS scientists' team on ... the facility and the culture to enable a successful startup into GMP manufacturing operations._ **Job Overview** The TS/MS organization provides technical oversight… more
- Lilly (Plainfield, IN)
- …implementation of appropriate countermeasures when needed in a timely manner. + Ensure GMP quality plan items are implemented appropriately. + Ensure inventory ... employees; for ensuring that warehouse operations are conducted in a high quality , regulatory-compliant manner; for maintaining the security of people and products;… more
- Bristol Myers Squibb (Indianapolis, IN)
- …Sr. Associate Scientist Radiochemist - Isotope Production, reporting to the Associate Director of Radiopharmaceuticals, will be an integral part of bringing ... innovative drug products to patients in need. As Sr. Associate Scientist, Radiochemist - Isotope Production, you will be...up GMP production. + Ensure compliance with GMP and NRC regulations, safety guidelines, and quality… more
- Lilly (Lebanon, IN)
- …+ When required (and per delegation procedure), in the absence of the Associate Director -Manufacturing provide continuity to the Process Team activities and ... role in implementing new technologies and operational process improvements in the GMP manufacturing environment. **As a Manufacturing Operations Associate , your… more
- Lilly (Indianapolis, IN)
- …for people around the world. **Position Brand Description:** The Operations Associate (OA) is responsible for ensuring operational excellence and continuous ... improvement. The Operations Associate will primarily serve the manufacturing site process teams, as well as support the Flow Team. They will work closely with… more
- Lilly (Lebanon, IN)
- …cycle time. + Coordinate housekeeping and fit and finish programs. + Assist Operations Associate and Operations Associate Director in planning and scheduling ... build the processes and facility to enable a successful startup into GMP manufacturing operations. **Position Brand Description:** The Quality Improvement… more
- Bristol Myers Squibb (Indianapolis, IN)
- …leader in radiopharmaceuticals. The Supervisor - Isotope Production, reporting to the Associate Director - Radiopharmaceuticals, will be an integral part of ... operators responsible for producing RayzeBio's radioisotopes under Good Manufacturing Practices ( GMP ). Additionally, you will be the front line in ensuring… more
- Lilly (Indianapolis, IN)
- …PPE. + Sr. Principal/Advisor level is considered equivalent to QA Associate Director for the purposes of Quality Assurance Approval The job specification is ... Support, Process Optimization & Continuous Improvement, Developing and Sustaining Quality Systems, and Adherence to Business Systems. **Key Objectives/Deliverables:**… more