• Quality Manager

    Vantage Specialty Chemicals (Gurnee, IL)
    …site maintains its quality registrations eg ISO 9000; passes all regulatory and customer audits ; and ensures the site meets cGMP and IPEC requirements and good ... **Position Summary** The purpose of the Quality Manager is to lead and maintain the site...and foster collaboration. + In-depth knowledge of ISO 9000, cGMP , IPEC, COSMOS, RSPO and relevant certification standards. +… more
    Vantage Specialty Chemicals (05/02/25)
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  • Senior Manager , Third Party Manufacturing

    Abbott (Buffalo Grove, IL)
    …medicines. Our 114,000 colleagues serve people in more than 160 countries. **Sr. Manager , Third Party Manufacturing** **Working at Abbott** At Abbott, you can do ... **The Opportunity** Abbott Diabetes Care has an opportunity for a Senior Manager , Third Party Manufacturing. The Senior Manager , Third Party Manufacturing… more
    Abbott (05/20/25)
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  • Validation Analyst II

    PCI Pharma Services (Rockford, IL)
    …Responsible for the generation and execution of validation protocols, assistance in audits , and the determination of validation needs. This job has no supervisory ... as required. Prepares change control and validation history report for audits . Attends conference calls and meetings. Effectively communicates project goals and… more
    PCI Pharma Services (06/18/25)
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  • Quality Systems Associate

    Grifols Shared Services North America, Inc (Wood River, IL)
    …Performs documentation review for unsuitable test results. * Assists the Quality Systems Manager to ensure that cGMP regulation, SOPs and regulatory requirements ... 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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  • Quality Specialist

    CSL Plasma (Waukegan, IL)
    **The Opportunity** This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance ... the development and implementation of continuous improvement plans + Collaborate with Assistant Manager of Quality (AMQ), to be able to represent the center during… more
    CSL Plasma (06/05/25)
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  • Utilities Engineer

    CSL Behring (Kankakee, IL)
    …groups they support. + Role that this position reports to: Sr. Manager , Water Operations **Responsibilities:** 1. Technical lead accountable for the operational ... systems to monitor, trend and verify equipment performance and downtime 4. Ensure cGMP compliance of all utility systems to meet regulatory compliance: + Equipment… more
    CSL Behring (06/24/25)
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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 been...+ 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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  • Phlebotomist

    Kedplasma (Springfield, IL)
    …of the donor during the plasmapheresis process under the direction of Center Manager . Operates within the scope of EU Guidance on Good Manufacturing Practice and ... FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has been...to the donor. + Prepares plasma collection center for audits by maintaining a clean, efficient work environment times… more
    Kedplasma (07/10/25)
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  • Medical Screener

    Kedplasma (Springfield, IL)
    …Responsible for registering and screening 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 been...issues or concerns. + Assists plasma collection center for audits . + Follows all SOPs and regulatory policies and… more
    Kedplasma (07/10/25)
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  • Clinical Label Control Coordin

    PCI Pharma Services (Rockford, IL)
    …in Clinical trial operation planning meetings as required, interact with project manager , QC/QA, production, planning, validation and warehouse to ensure that jobs ... + Assisting in the hosting of external and internal audits of the Labeling Department + Complete component specification,...possible. + Knowledge of and adherence to all PCI, cGMP , and GCP policies, procedures, rules. + This position… more
    PCI Pharma Services (07/16/25)
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