• Supervisor , Manufacturing

    Catalent Pharma Solutions (Harmans, MD)
    **We're hiring a Supervisor , Batch Record Review, to** **provide oversite of documentation support for all pharmaceutical manufacturing activities in** ... of life-enhancing and life-saving treatments for patients annually. The ** Supervisor , Batch Record Review** is...to execute the review and successful release of all batch records used in Catalent manufacturing more
    Catalent Pharma Solutions (12/21/24)
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  • Supervisor , Upstream Manufacturing

    Catalent Pharma Solutions (Harmans, MD)
    …teams to execute procedures for upstream manufacturing and support area of manufacturing using SOP's and batch records . Operating production equipment ... ** Supervisor , Manufacturing ** **Summary:** _Catalent, Inc. is...management for direct reports. + Draft and revise official manufacturing documents, SOPs, Batch Records ,… more
    Catalent Pharma Solutions (12/17/24)
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  • Downstream Manufacturing Group Lead (AM…

    Catalent Pharma Solutions (Harmans, MD)
    manufacturing operations and documentation and adhering to safety guidelines + Completes Batch Production Records under cGMP, and documents in detail using ... ** Manufacturing Group Lead** **Summary:** _Catalent, Inc. is a...+ Excellent documentation skills including comprehension, review & establishing Batch Production Records , SOP's, deviation & summary… more
    Catalent Pharma Solutions (12/13/24)
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  • Supervisor , QA OTF

    Catalent Pharma Solutions (Harmans, MD)
    …procedures and batch records , providing real time review of manufacturing batch record documentation and logbooks, and working with operations ... relevant procedures; monitor, participate and oversee the real time batch record review process, including escalation of...Ensure manufacturing compliance with applicable procedures and batch records ; review manufacturing shop… more
    Catalent Pharma Solutions (12/18/24)
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  • Supervisor , Client QA

    Catalent Pharma Solutions (Harmans, MD)
    …include tracking and reviewing technology transfer documents, specifications, master batch records , change requests, deviations and failure investigations ... The ** Supervisor , Client QA** is responsible for providing QA...of Client Projects from start to finish for GMP Manufacturing of master/working cell banks, biological bulk drug substance… more
    Catalent Pharma Solutions (12/03/24)
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  • Associate Scientist III, Process Development…

    Catalent Pharma Solutions (Baltimore, MD)
    …standard operation procedures, protocols, and maintains training + Manages data, and completes batch records , experimental records according to GDP + ... Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply… more
    Catalent Pharma Solutions (12/24/24)
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