• Associate Director, MSAT, Upstream

    Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
    …compliance of upstream operations through effective technology transfer, validation support, process monitoring, troubleshooting, and lifecycle management activities ... trends, and propose process improvements. + Support process characterization and validation activities (PPQ) for upstream processes executed at CDMOs. + Evaluate… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
    - Related Jobs

  • Senior Statistical Programmer FSP

    Cytel (Indianapolis, IN)
    **Sponsor-dedicated:** Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our ... you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next...listings, and figures (TLFs) + Production and QC / validation programming + Generating complex ad-hoc reports utilizing raw… more
    Cytel (07/30/25)
    - Related Jobs

  • Senior Statistical Programmer FSP

    Cytel (Indianapolis, IN)
    **Sponsor-dedicated:** Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our ... you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next...(ISS/ISE), utilizing SAS programming + Production and QC / validation programming + Generating complex ad-hoc reports utilizing raw… more
    Cytel (07/24/25)
    - Related Jobs

  • Principal Biostatistician FSP - Chemistry,…

    Cytel (Indianapolis, IN)
    …to do the same. **Sponsor-dedicated:** Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at ... As a Biostatistician you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment,… more
    Cytel (07/18/25)
    - Related Jobs

  • Advisor - Chemistry (R5-R6)

    Lilly (Indianapolis, IN)
    …in-process, release, characterization analysis and stability testing of active pharmaceutical ingredient and drug products. Introduce new methodologies for ... responsible experience with product development within a laboratory or pharmaceutical manufacturing environment and Good Manufacturing Practice (GMP). Experience… more
    Lilly (06/12/25)
    - Related Jobs

  • Manager, QA ( PM or Weekend Shift )

    Novo Nordisk (Bloomington, IN)
    …6 weeks paid family medical leave + Free access to Novo Nordisk-marketed pharmaceutical products + Tuition Assistance + Life & Disability Insurance + Employee ... oversight of the equipment calibration and preventive maintenance program and validation activities. Quality Assurance Operations group has oversight of the… more
    Novo Nordisk (06/03/25)
    - Related Jobs

  • Advisor, Contamination Control Strategy - Lebanon…

    Lilly (Lebanon, IN)
    …the initial start-up of the manufacturing areas as well as post Process Validation support. + Understand and support global implementation of quality standards, best ... contamination control: manufacturing facilities, production practices, equipment cleaning and validation , environmental monitoring, bioburden controls and other product protection… more
    Lilly (05/21/25)
    - Related Jobs

  • Principal Representative, QA-Data Integrity

    Novo Nordisk (Bloomington, IN)
    …6 weeks paid family medical leave + Free access to Novo Nordisk-marketed pharmaceutical products + Tuition Assistance + Life & Disability Insurance + Employee ... Assist with the development, execution and approval of System and Validation Lifecycle Documentation for site GxP systems, including specifications, test protocols,… more
    Novo Nordisk (07/24/25)
    - Related Jobs

  • Supervisor, Quality Control Chemistry

    Cardinal Health (Indianapolis, IN)
    …with 21 CFR 210, 211 in the FDA regulated industry preferred ( Pharmaceutical or Medical Device). + Must have experience with equipment qualification, software ... validation , test method validation , and/or process validation preferred. + Has experience in authoring a variety of documentation such as SOPs, Change… more
    Cardinal Health (07/18/25)
    - Related Jobs

  • Sr. Scientist, Product Development

    Cardinal Health (Indianapolis, IN)
    …selection, process and analytical equipment configuration, document creation, method validation , and process qualification, as well as occasional production and ... testing activities typical for a cGMP pharmaceutical manufacturing operation including the preparation of chemicals and...of experience working in a GMP environment in the pharmaceutical or biotechnology industry. A background in product research… more
    Cardinal Health (07/18/25)
    - Related Jobs