• Scientist I, Chemistry, Manufacturing, and Control…

    Cardinal Health (Springfield, IL)
    …Manufacturing, and Control (CMC)_ ensures efficient and quality production of product submission dossiers for Cardinal Health's Regulatory Science clients. ... + Drafts submissions for products, ensuring that all relevant product and client information and data is communicated in...and presentations for clients. May serve as a project manager for smaller projects and ensure that team members… more
    Cardinal Health (06/25/25)
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  • Food Quality Technician

    Sysco (Hampshire, IL)
    …to ensure compliance of products and processes to corporate and regulatory requirements at a Sysco Specialty Meat and/or Seafood Company. **RESPONSIBILITIES** ... supplier program, foreign material control, plant sanitation, chemical control, product quality assurance, FSQA Customer complaints, food defense and security… more
    Sysco (07/02/25)
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  • Plasma Processor

    Kedplasma (Urbana, IL)
    …and storage of plasma collected from donors under the direction of the Center Manager . Operates within the scope of EU Guidance on Good Manufacturing Practice and ... FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has...AND RESPONSIBILITIES** **Core** + Maintains safety and integrity of product and samples during processing, storage, and shipment release… more
    Kedplasma (07/10/25)
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  • Processing Lead

    Kedplasma (Urbana, IL)
    …levels, and Specialty Programs (where applicable) under the direction of the Center Manager . Operates within the scope of EU Guidance on Good Manufacturing Practice ... and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has...placement of units/samples into freezer per SOPs to ensure product quality. + Performs troubleshooting of equipment within scope… more
    Kedplasma (06/24/25)
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  • Business Development Mgr, ESD (East Coast)

    Fujifilm (Springfield, IL)
    …States. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... the Endoscopy space. The role of the Business Development Manager is to understand and define our internal and...marketing organization. The incumbent is responsible for supporting the product management group including, but not limited to market… more
    Fujifilm (04/25/25)
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  • Lead, Sanitation

    Barry Callebaut (Chicago, IL)
    …company, serving the entire food sector, from the cocoa bean to the finest chocolate product . We are a company with a purpose, we believe in doing well by doing ... Values and of course loving chocolate. Under the direction of the Operations Manager , the Sanitation Lead will be accountable for accomplishing food safety hygiene… more
    Barry Callebaut (07/08/25)
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  • Quality Systems Associate

    Grifols Shared Services North America, Inc (Wood River, IL)
    …Quality Systems Manager to ensure that cGMP regulation, SOPs and regulatory requirements are followed. Duties include: Under the direct supervision of the ... with us! **Summary:** Under the direct supervision of the Quality Systems Manager , perform quality assurance and Training functions to ensure compliance with… more
    Grifols Shared Services North America, Inc (07/09/25)
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  • Lead Project Team Support Engineer

    Fujifilm (Springfield, IL)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... variable factors which may include customer impact, HCUS business priorities and regulatory requirements. Provides to assistance to all connected teams on technical… more
    Fujifilm (05/08/25)
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  • Training Coordinator

    Kedplasma (Chicago, IL)
    …within the assigned plasma collection center under the direction of the Center Manager . Operates within the scope of EU Guidance on Good Manufacturing Practices and ... FDA cGMP 21CFR. **ESSENTIAL JOB SUNCTIONS** Every effort has...+ Works in coordination with the Regional Field Training Manager for training-related initiatives. + Demonstrates competence and compliance… more
    Kedplasma (07/18/25)
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  • Sr Synapse Sys Admin Trainer

    Fujifilm (Springfield, IL)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... to: customer facing course material, instructional "how to" videos, product simulations, etc. + Responsible for executing all aspects...in the event of Senior II, Lead SSAT and manager absence. + Maintain close contact with customers for… more
    Fujifilm (06/10/25)
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