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Lilly
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Durham, North Carolina
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better for people around the world.
Associate Director - Quality Assurance (QA) Packaging is ... processes in the Device Assembly and Packaging (DAP) production area at Lilly RTP. The Associate Director
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Lilly
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Indianapolis, Indiana
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and/or experience in API or finished product manufacturing, QA or Engineering.
**Additional ... perform QA responsibilities of API shipments.
Participate in regulatory inspection preparations with
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Lilly
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Indianapolis, Indiana
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Additional Skills/Preferences:
Experience in TS/MS, Engineering, QC and/or QA is preferred with ... the site inspection readiness program and assist and advice the lead investigators, functional leaders
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Lilly
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Concord, North Carolina
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to a team of QA Specialists, while reporting directly to the Associate Director – QA Parenteral. The ... formulation, filling and visual inspection process areas. The QA Floor Support Lead works along with their
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Lilly
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Indianapolis, Indiana
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quality oversight of Indianapolis Parenteral Manufacturing’s central quality processes.
The Associate Director for Site Quality & Compliance is responsible for managing the activities of Quality
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Lilly
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Pleasant Prairie, Wisconsin
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management to evaluate proposed manufacturing processes and associated controls with respect to the potential ... – Sterility Assurance – Technical Services/Manufacturing Science (TS/MS) role is a technical position that
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Lilly
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Lebanon, Indiana
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constructing an advanced manufacturing facility for production of API (Active Pharmaceutical Ingredient) molecules located in Lebanon, IN. This facility is Lilly’s largest investment in manufacturing capacity and
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Lilly
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Concord, North Carolina
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from Engineering, Maintenance, Technical Services / Manufacturing Sciences (TS/MS), Quality, and Health ... Associate Director (AD), Operations is responsible for staffing, training, and leadership of the operations
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Lilly
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Durham, North Carolina
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, with a focus on Automated Warehouse operations. This role reports directly to the Associate Director ... , procedures, technical studies, validation protocols, change controls, and engineering documents
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