• Associate Director, Small Molecule Process…

    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 ... 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 (08/19/25)
    - Related Jobs
  • Quality Specialist I

    Catalent Pharma Solutions (Greendale, IN)
    …English. Ability to communicate with all line level positions and management. + Knowledge of GMP and Quality systems. + The employee must be able to lift and/or ... ** Quality Specialist I** **Position Summary** Catalent, Inc. is...help create engaging new products consumers will love. The ** Quality Specialist I** is responsible for auditing the products… more
    Catalent Pharma Solutions (08/26/25)
    - Related Jobs
  • Senior Project Engineer

    Nestle (Anderson, IN)
    …collection and feedback process for projects. + Monitors processes for compliance with quality and GMP requirements in accordance with FDA and OSHA regulations. ... own initiative, without first questioning its impact in relation to product safety/ quality , people safety and the environment. No compromises will be tolerated.… more
    Nestle (08/16/25)
    - Related Jobs
  • Project Engineering Manager

    Nestle (Anderson, IN)
    …collection and feedback process for projects. + Monitors processes for compliance with quality and GMP requirements in accordance with FDA and OSHA regulations. ... own initiative, without first questioning its impact in relation to product safety/ quality , people safety and the environment. No compromises will be tolerated.… more
    Nestle (08/14/25)
    - Related Jobs
  • Director - QA Iapi

    Lilly (Indianapolis, IN)
    …and implement the site continuous improvements, site business plan objectives, and GMP Quality Plan objectives + Provide coaching/feedback to and develop ... for people around the world. #WeAreLilly **Responsibilities:** The Associate Director - Quality Assurance (QA) is responsible for managing the activities of QA… more
    Lilly (08/19/25)
    - Related Jobs
  • Lab Technician

    Actalent (Mount Vernon, IN)
    …Ability to work effectively both independently and as part of a team. + Experience in Quality Control, Quality Assurance, and GMP . + Skills in GC-MS, HPLC, ... conducting various chemical analyses and tests to ensure the quality and compliance of our products. This role is...in research and development projects aimed at improving product quality and performance. + Prepare and present detailed reports… more
    Actalent (08/19/25)
    - Related Jobs
  • Additive Manufacturing Engineer II

    Ricoh Americas Corporation (Indianapolis, IN)
    …documentation, operator training. Collaborate with Quality Engineering to develop quality plans ensuring GMP compliance. Operate 3D printers and ... process documents, and transfer to production. Lead projects to improve quality , process stability, and reduce cost while meeting customer requirements. Develop… more
    Ricoh Americas Corporation (07/31/25)
    - Related Jobs
  • Quality Lab Technician

    Actalent (Richmond, IN)
    …various microbiological and chemical testing methods. + Familiarity with food safety and quality standards, including SQF, HACCP, and GMP . + Strong attention to ... tasks simultaneously. Additional Skills & Qualifications + Laboratory expertise + Quality assurance knowledge + Proficiency in GMP , Biology, Microbiology,… more
    Actalent (08/27/25)
    - Related Jobs
  • QA Engineer, Foundry

    Lilly (Lebanon, IN)
    …Foundry, including benchmarking with other Lilly sites. + Evaluate potential product quality impact for any GMP -related incident (deviation or change control), ... and computer systems (CSQ) within the Foundry and assures compliance with quality systems and current Good Manufacturing Practices (cGMP). This oversight includes… more
    Lilly (08/27/25)
    - Related Jobs
  • Associate Director - Device Commercialization

    Lilly (Indianapolis, IN)
    …skills + Familiarity and practical experience with medical device / combination product quality & regulatory requirements, including GMP /CFR, EU MDR, ISO and IEC ... and gap assessment coordination and resolution. **Key Objectives/Deliverables:** Safety and Quality + Ensure staff is current with all relevant, required training… more
    Lilly (08/27/25)
    - Related Jobs