- Lilly (Indianapolis, IN)
- …groups such as Global Facilities Delivery (GFD) and Global Quality. **Responsibilities:** The Associate Director - Global Process Automation & Control ... improvement, and overall customer service for the team. The Associate Director role will provide process...Technical expertise in one or more automation platforms. + cGMP Regulatory knowledge in process or automation… more
- Lilly (Lebanon, IN)
- …enable a successful startup into GMP manufacturing operations. **Position Description:** The ** Associate Director Process Engineering - Peptides Active ... equipment and systems are used in the manufacturing of peptide products. Additionally, the Associate Director of Process Engineering - Peptides leads this … more
- Bristol Myers Squibb (Indianapolis, IN)
- …team, RayzeBio aims to be the global leader in radiopharmaceuticals . The Associate Director of Validation is responsible for leading the validation function ... your application should be directed to Chat with Ripley. R1595528 : Associate Director of Validation **Company:** Bristol-Myers Squibb **Req Number:** R1595528… more
- Lilly (Indianapolis, IN)
- …as we achieve drug product manufacturing and commercialization excellence. As the Associate Director of Technical Services/Manufacturing Science (TS/MS) in the ... + **Technical Excellence:** Lead and provide technical and effective process support services for production issue resolution and investigations, ensuring… 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 ... 4. Technical Excellence: Lead and provide technical input and effective process support for manufacturing issue resolution and investigations, champion continuous… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- **Job Summary** The Associate Director Controlled Substances, Quality Global Product Quality - API/DP is responsible for directing quality oversight of clinical ... stored, and transported accordance with regulatory expectations and applicable cGMP /GDP quality standards. This role has global responsibility for directing… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products at ... way that is in accordance with regulatory expectations and applicable cGMP /GDP quality standards. This role will direct Biologics Quality Assurance support,… more
- Lilly (Lebanon, IN)
- …impact to our environment. **What You'll Be Doing** The Manufacturing & Quality (MQ) IT Associate Director -IT for LP2 will serve as the leader for the IT ... + Provide leadership in the development and execution of cGMP and/or improvement plans within the IT function and...to request an accommodation as part of the application process and any other correspondence will not receive a… more
- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. ** Associate Director - Digital Engineering Solutions** **Organization Overview:** At Lilly, ... twins, computational modeling, edge/IoT, and analytics solutions. **Responsibilities:** The Associate Director - Digital Engineering Solutions position, within… more
- Bristol Myers Squibb (Indianapolis, IN)
- …your application should be directed to Chat with Ripley. R1596697 : Associate Director , IT Regulatory, Clinical, and Enterprise Systems **Company:** ... aims to be the global leader in radiopharmaceuticals. **Job Description** The Assoc. Director , IT Regulatory, Clinical and Enterprise Systems is an integral part of… more
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