• Associate Representative, Quality Assurance

    Novo Nordisk (Bloomington, IN)
    …6 weeks paid family medical leave + Free access to Novo Nordisk-marketed pharmaceutical products + Tuition Assistance + Life & Disability Insurance + Employee ... High School diploma or equivalent education with minimum 4 years of pharmaceutical production/QA/QC experience, required. + Little to no experience required with… more
    Novo Nordisk (08/20/25)
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  • Principal Database Developer

    Cytel (Indianapolis, IN)
    …systems can achieve. **Sponsor-dedicated:** Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be ... you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next...Sources + Clinical Coding + SAE Reconciliation + Data Validation and Quality Control + Blinding and Unblinding Procedures… more
    Cytel (08/14/25)
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  • Pharmacist - NICU

    Parkview Health (Fort Wayne, IN)
    …in a variety of areas for decades. Parkview offers a progressive pharmaceutical care environment in a variety of practice settings. Inpatient services include ... pharmacies. We have also had tremendous growth in ambulatory pharmaceutical care including primary care, hospital-based clinics, specialty clinics, multiple… more
    Parkview Health (08/07/25)
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  • Medication Safety Coordinator

    Parkview Health (Fort Wayne, IN)
    …in a variety of areas for decades. Parkview offers a progressive pharmaceutical care environment in a variety of practice settings. Inpatient services include ... pharmacies. We have also had tremendous growth in ambulatory pharmaceutical care including primary care, hospital-based clinics, specialty clinics, multiple… more
    Parkview Health (08/07/25)
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  • Manager, Biostatistics

    Sumitomo Pharma (Indianapolis, IN)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... on SDTM/ADaM datasets and TLF specifications. + Perform programming validation for key derived datasets and oversee Quality Control...by law. Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in… more
    Sumitomo Pharma (08/02/25)
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  • IDM Asset Delivery Process Engineer

    Lilly (Indianapolis, IN)
    …the automated device assembly equipment design, delivery, and qualification/ validation . **Responsibilities:** + Technical Proposal Assessment: Assess technical ... + Minimum 2 years engineering experience, preferably in medical device, pharmaceutical , or related industry working with high speed, discrete mechanical/process… more
    Lilly (08/01/25)
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  • Sr. Specialist, Quality Assurance

    Cardinal Health (Indianapolis, IN)
    …of quality, analytical metrics and / or statistics, trending, quality planning, validation , CAPA and problem solving. + Works cross-functionally and has the ability ... working with 21 CFR 210, 211 in the FDA regulated industry ( Pharmaceutical or Medical Device) preferred + Possess an understanding of cGMP/compliance requirements… more
    Cardinal Health (07/31/25)
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  • Senior Director - Drug Supply Chain Security Act…

    Lilly (Indianapolis, IN)
    …for ensuring the integrity, traceability, and regulatory compliance of our pharmaceutical supply chain, while also driving continuous improvement in quality systems ... at all times. + Technology & Data Governance: Oversee implementation and validation of serialization and EPCIS data exchange platforms (eg, TraceLink, SAP ATTP).… more
    Lilly (07/08/25)
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  • Visual Inspection Subject Matter Expert-…

    Lilly (Indianapolis, IN)
    …detail-oriented Visual Inspection Subject Matter Expert (SME) specializing in parenteral pharmaceutical products. The SME will be responsible for overseeing and ... documents (Global Q standards, Common Q practices, ) and execution documents ( validation reports, PoDs ) to support the visual inspection Quality System.… more
    Lilly (06/14/25)
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  • Sr. Scientist - TS/MS - Dry EM

    Lilly (Indianapolis, IN)
    …technical reports, change controls, regulatory submissions, deviation investigations, validation protocols and summary reports, processing records, procedures, PFDs, ... Qualifications:** + Bachelor's Degree in scientific disciplines of Pharmacy, Pharmaceutical Science, Pharmaceutical Engineering, Biochemistry, Organic Chemistry,… more
    Lilly (06/12/25)
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