• Novo Nordisk Inc. (West Lebanon, IN)
    …The Position The person in this role will also be responsible for validation activities in several areas of pharmaceutical manufacturing including, but not ... sciences or engineering Work Experience A minimum of three (3) years validation experience in the pharmaceutical or biotechnology industry Experience preparing… more
    HireLifeScience (05/17/25)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …of two (2) years related experience. Prefer medium to large scale pharmaceutical or biotechnology process experience Knowledge, Skills, and Abilities Ability ... option 14 weeks Paid Parental Leave Free access to Novo Nordisk-marketed pharmaceutical products At Novo Nordisk, you will find opportunities, resources and… more
    HireLifeScience (06/27/25)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …representative for contractor services including design, fabrication, installation, and validation Point person for process improvement activities, including ... Experience A minimum of seven (7) years' experience in medium to large scale pharmaceutical or biotechnology process is required with a Bachelor's degree. At… more
    HireLifeScience (05/17/25)
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  • LanceSoft (Indianapolis, IN)
    Job Title: Senior Validation Engineer Pay Rate: - Location: Onsite Job Description Summary: This individual will execute engineering activities (design, ... project objectives. Responsible for execution of Commissioning, Qualification and Validation (CQV) activities for facility, utilities and manufacturing equipment.… more
    Upward (06/29/25)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …option 14 weeks Paid Parental Leave Free access to Novo Nordisk-marketed pharmaceutical products At Novo Nordisk, you will find opportunities, resources and ... projects and other related support activities for the manufacturing facility and process . This individual works with supervision on routine tasks and detailed… more
    HireLifeScience (05/08/25)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …option 14 weeks Paid Parental Leave Free access to Novo Nordisk-marketed pharmaceutical products At Novo Nordisk, you will find opportunities, resources and ... connected and functional Work with PM to conduct system testing and validation to ensure proper operation Programming and Configuration Assist with contractors to… more
    HireLifeScience (04/26/25)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    … improvements/cost reduction program into manufacturing Perform area equipment and process validations in accordance with validation procedures Perform in- ... option 14 weeks Paid Parental Leave Free access to Novo Nordisk-marketed pharmaceutical products At Novo Nordisk, you will find opportunities, resources and… more
    HireLifeScience (07/09/25)
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  • Eli Lilly and Company (Indianapolis, IN)
    …and delivering custom assembly equipment used as part of the manufacturing process . These equipment deliveries support new product launches, capacity expansions and ... Contract Manufacturing receiving sites across the globe. IDM Asset Delivery Process Engineers are responsible for providing technical support for developing,… more
    Upward (07/07/25)
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  • Eli Lilly and Company (Indianapolis, IN)
    …detail-oriented Visual Inspection Subject Matter Expert (SME) specializing in parenteral pharmaceutical products. The SME will be responsible for overseeing and ... the internal and external manufacturing network. Technical Expertise & Process Optimization : Serve as the go-to expert on...Q standards, Common Q practices, ) and execution documents ( validation reports, PoDs ) to support the visual inspection… more
    Upward (06/27/25)
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  • Senior Validation Engineer - Pharma

    PDS Tech Commercial, Inc. (Indianapolis, IN)
    …Commercial is looking for a highly motivated and experienced **Senior Validation Engineer** to support a leading-edge pharmaceutical manufacturing environment ... process and equipment issues during startup, PQ, and validation + Support the setup of maintenance plans, spare...or a related technical field + 5+ years of validation or engineering experience in a GMP-regulated pharmaceutical more
    PDS Tech Commercial, Inc. (07/23/25)
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