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Ideally, knowledge of SAP EWM or experience as a Key User, Super User, or Power User of an ERP or Warehouse Management System. Join us and play an important role in connecting operations, customer key users, and IT while actively shaping reliable SAP EWM-driven processes. * Bridging Operations, IT, and Customer requirements: Coordinate collaboration between operational teams, customer key users, and the IT department to ensure effective communication and issue resolution. Communicate new functionalities and process changes in a clear, practical, and user-friendly manner. * Arvato Austria GmbH * Kronstorf * Feste Anstellung * Vollzeit - Together - We' re on it! Arvato is an innovative and leading global 3PL service provider in supply chain management and e-commerce. Wi
Ideally, knowledge of SAP EWM or experience as a Key User, Super User, or Power User of an ERP or Warehouse Management System. Join us and play an important role in connecting operations, customer key users, and IT while actively shaping reliable SAP EWM-driven processes. * Bridging Operations, IT, and Customer requirements: Coordinate collaboration between operational teams, customer key users, and the IT department to ensure effective communication and issue resolution. Communicate new functionalities and process changes in a clear, practical, and user-friendly manner. * Arvato Austria GmbH * Kronstorf * Feste Anstellung * Vollzeit - Together - We' re on it! Arvato is an innovative and leading global 3PL service provider in supply chain management and e-commerce. Wi
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As a globally operating business we contribute to sustainable animal protein production by providing high tech and essential solutions in the areas of biosecurity, veterinary diagnostics, vaccines, in-vitro PCR diagnostica, and pharmaceuticals. * Produce high-quality semi-finished and finished diagnostic products according to established production processes and quality standards. * Prepare materials, reagents, buffers and production components to ensure smooth and efficient production workflows. * Perform in-process quality checks and accurately document all production activities in line with internal and ISO requirements. * Contribute to a clean, organized, and continuously improving production environment while supporting the onboarding of new team members. * First
As a globally operating business we contribute to sustainable animal protein production by providing high tech and essential solutions in the areas of biosecurity, veterinary diagnostics, vaccines, in-vitro PCR diagnostica, and pharmaceuticals. * Produce high-quality semi-finished and finished diagnostic products according to established production processes and quality standards. * Prepare materials, reagents, buffers and production components to ensure smooth and efficient production workflows. * Perform in-process quality checks and accurately document all production activities in line with internal and ISO requirements. * Contribute to a clean, organized, and continuously improving production environment while supporting the onboarding of new team members. * First
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Schnelle Bewerbung
ensure quality oversight for complex R&D projects and global quality initiatives * review, approve, and release GMP-relevant documentation and quality deliverables * drive quality activities including risk assessments, deviations, change controls, CAPAs, and training initiatives * provide expert guidance on cGMP compliance and quality standards * promote operational excellence and a strong quality culture across the organization * hold a Bachelor's degree with 5+ years or a Master's degree with 3+ years of experience in Pharma Quality, QA, Development, or Operations * have strong knowledge of cGMP regulations, quality systems, and regulatory requirements * bring experience in quality
ensure quality oversight for complex R&D projects and global quality initiatives * review, approve, and release GMP-relevant documentation and quality deliverables * drive quality activities including risk assessments, deviations, change controls, CAPAs, and training initiatives * provide expert guidance on cGMP compliance and quality standards * promote operational excellence and a strong quality culture across the organization * hold a Bachelor's degree with 5+ years or a Master's degree with 3+ years of experience in Pharma Quality, QA, Development, or Operations * have strong knowledge of cGMP regulations, quality systems, and regulatory requirements * bring experience in quality
Schnelle Bewerbung
ensure quality oversight for complex R&D projects and global quality initiatives * review, approve, and release GMP-relevant documentation and quality deliverables * drive quality activities including risk assessments, deviations, change controls, CAPAs, and training initiatives * provide expert guidance on cGMP compliance and quality standards * promote operational excellence and a strong quality culture across the organization * hold a Bachelor's degree with 5+ years or a Master's degree with 3+ years of experience in Pharma Quality, QA, Development, or Operations * have strong knowledge of cGMP regulations, quality systems, and regulatory requirements * bring experience in quality
ensure quality oversight for complex R&D projects and global quality initiatives * review, approve, and release GMP-relevant documentation and quality deliverables * drive quality activities including risk assessments, deviations, change controls, CAPAs, and training initiatives * provide expert guidance on cGMP compliance and quality standards * promote operational excellence and a strong quality culture across the organization * hold a Bachelor's degree with 5+ years or a Master's degree with 3+ years of experience in Pharma Quality, QA, Development, or Operations * have strong knowledge of cGMP regulations, quality systems, and regulatory requirements * bring experience in quality