• Associate Director, Global Product Quality

    Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
    …well as drive continuous improvement. **Job Description** + Responsible for directing quality oversight of GMP contract manufacturers of controlled substances ... **Job Summary** The Associate Director Controlled Substances, Quality Global Product Quality - API/DP...batch record review and release process for + OAPI GMP release of Contract Manufacturers operations supporting clinical and… more
    Otsuka America Pharmaceutical Inc. (12/19/25)
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  • Associate Director, Quality & Compliance

    Astrix Technology (Indianapolis, IN)
    …Apply for Job Associate Director, Quality & Compliance, you will **own GMP quality execution** for a commercial-scale sterile facility, build and scale QA/QC ... bar + A bias for action, accountability, and pragmatic GMP decision-making + Build quality systems that support **first-in-class cancer therapies** + Join a… more
    Astrix Technology (12/16/25)
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  • Associate Director Process Engineering - Peptides…

    Lilly (Lebanon, IN)
    …to influence and implement the technical agenda, site business plan objectives, and GMP Quality Plan objectives. + Identify, track, and report key indicators ... facility, and the culture to enable a successful startup into GMP manufacturing operations. **Position Description:** The **Associate Director Process Engineering -… more
    Lilly (10/29/25)
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  • Senior Specialist QA Operations

    Bristol Myers Squibb (Indianapolis, IN)
    …or other regulatory authorities is preferred. **Skills and Qualifications** + Expertise in GMP , Quality , material and product disposition + Strong capability in ... The Senior Specialist, QA Operations will help support operations through quality oversight in a Radiopharmaceutical facility in Indianapolis, IN. The Senior… more
    Bristol Myers Squibb (12/18/25)
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  • PRD - Early Phase QA - Advisor/Sr. Advisor

    Lilly (Indianapolis, IN)
    …world. **Position Brand Description:** Early Phase Quality Assurance is accountable for GMP Quality dedicated to the PR&D Early Phase Team. This position is ... in, continuous improvement + Ensure inspection readiness through site self-assessments, GMP education, monitoring, establishing and enhancing Quality systems and… more
    Lilly (12/17/25)
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  • Associate Director - TS/MS - Lebanon API

    Lilly (Lebanon, IN)
    …to influence and implement the technical agenda, site business plan objectives, and GMP Quality Plan objectives. + Interact with regulators, customers, or other ... facility and the culture to enable a successful startup into GMP manufacturing operations._ **Position Description:** The Associate Director - Technical… more
    Lilly (10/14/25)
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  • Quality Engineer I

    Tecomet (Claypool, IN)
    …and Abilities:** + Manufacturing operations - forging and/or machining. + Measuring devices. + Quality Systems. + Regulations - FDA, GMP and ISO. + Blueprint ... Type** Full-time **Salaried/Hourly** Salaried **Travel Requirements** 10% **Job Description** Quality Engineer I **Position Summary** The Quality Engineer… more
    Tecomet (11/19/25)
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  • Blowmolding Technician

    Graham Packaging Company (Evansville, IN)
    …an Operator include: + Understands, follows and enforces all established safety, health, quality GMP and Company policies, procedures and recognized practices. + ... established policies, procedures and recognized practices. + Participate in continuous quality improvement projects and other related activities as assigned +… more
    Graham Packaging Company (12/03/25)
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  • Bioassay Analyst

    Eurofins US Network (Indianapolis, IN)
    …assay, cell biology skills such as cell culturing, cell counting, cell banking; GMP quality system and lab operations experience + Excellent communication (oral ... surrogate bioassays such as ligand-binding ELISA assays in plate-based format in a GMP environment + Perform qualification and transfer of analytical test methods in… more
    Eurofins US Network (12/30/25)
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  • Associate Director, Small Molecule Process…

    Lilly (Indianapolis, IN)
    …to influence and implement the technical agenda, site business plan objectives, and GMP Quality Plan objectives. + Identify, track, and report key indicators ... the necessary systems and business processes required to support GMP operations, and build the site culture. This will...the site evolves from a design concept to a GMP clinical trial site. **Key Responsibilities:** + Responsible for… more
    Lilly (11/13/25)
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