- Astrix Technology (Indianapolis, IN)
- ** Associate Director , Quality & Compliance** ...15/12/2025 Apply for Job Associate Director , Quality & Compliance, you will **own GMP ... bar + A bias for action, accountability, and pragmatic GMP decision-making + Build quality systems that support **first-in-class cancer therapies** + Join a… 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 ... as well as drive continuous improvement. **Job Description** + Responsible for directing quality oversight of GMP contract manufacturers of Otsuka clinical and… 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 ... well as drive continuous improvement. **Job Description** + Responsible for directing quality oversight of GMP contract manufacturers of controlled substances… more
- Lilly (Indianapolis, IN)
- …us to develop creative solutions to support communities through philanthropy and volunteerism. The Associate Director - Quality Control leads all aspects of ... fast-paced environment, while delivering on multiple priorities. + Apply knowledge of quality principles and GMPs toward the development of local procedures. +… more
- Lilly (Lebanon, IN)
- …startup into GMP manufacturing operations. **Position Description:** The ** Associate Director Process Engineering - Peptides Active Pharmaceutical ... used in the manufacturing of peptide products. Additionally, the Associate Director of Process Engineering - Peptides...implement the technical agenda, site business plan objectives, and GMP Quality Plan objectives. + Identify, track,… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- The Associate Director of Global Supplier Quality will be responsible for the execution of supplier quality audit and monitoring across the company's ... , with 2+ years in supplier or external manufacturing quality . + Strong knowledge of GMP regulations...external manufacturing quality . + Strong knowledge of GMP regulations for small molecules and/or biologics. + Experience… more
- Lilly (Lebanon, IN)
- …startup into GMP manufacturing operations._ **Position Description:** The Associate Director - Technical Services/Manufacturing Science (TSMS) is responsible ... for managing the activities of TSMS personnel. The Associate Director TSMS must balance coaching a...implement the technical agenda, site business plan objectives, and GMP Quality Plan objectives. + Interact with… more
- Lilly (Indianapolis, IN)
- …for clinical trial medicines, while also reducing costs and environmental impact. The Associate Director of Materials will lead the planning and procurement of ... and regulatory changes. + Ensure all activities comply with GMP , GDP, and site quality standards. +...activities comply with GMP , GDP, and site quality standards. + Develop contingency strategies for critical clinical… more
- Lilly (Lebanon, IN)
- …into GMP manufacturing operations. **Description:** The **Project Engineering Associate Director ** at Lebanon API Manufacturing provides leadership and ... and implement the necessary systems and business processes required to support GMP operations, and build the site culture. This will require significant… more
- Lilly (Indianapolis, IN)
- …clinical trial medicines, while also reducing costs and environmental impact. The Associate Director Small Molecule Process Engineering provides leadership and ... influence and implement the technical agenda, site business plan objectives, and GMP Quality Plan objectives. + Identify, track, and report key indicators of… more