Vikrant Deshmukh
Vikrant Deshmukh
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Systems Process Specialist ITOT, Genentech
California, United States
Proven expertise and implementation experience in manufacturing and production environments, with proficiency in configuring SAP/MES solution for the MAKE (Manufacturing/Produce Product) process, particularly in regulated environments, and a strong understanding of manufacturing execution, quality control, and supply chain processes within SAP. Demonstrated strong understanding of SAP's batch management, lot traceability, production order management, and quality control features, with experience in manufacturing workflows, document management systems, and quality management processes in Life Sciences.
Committed to process optimization and continuous improvement by staying up-to-date with industry trends, SAP and MES updates, and regulatory changes while actively seeking opportunities to improve manufacturing processes, streamline operations, and enhance system efficiency. Apply analytical and problem-solving skills with lean techniques and modern manufacturing processes, including data analytics, AI, visualization, and error proofing.
Skilled in systems integration and architecture, ensuring the compatibility, integration, interoperability, stability, scalability, and usability of products and services proposed as standards to ensure an integrated architecture across interdependent technologies. Extracted insights from key shop floor manufacturing systems like MES, SCADA, IoT devices, and PLCs while leveraging analytical tools to pinpoint and implement improvements across various operational processes.
Demonstrated expertise in regulatory compliance and industry standards, including familiarity with GxP, FDA regulations, 21 CFR Part 11, and other relevant industry standards. Possesing solid understanding of the Life Sciences industry, specifically the challenges and regulatory considerations related to batch release, manufacturing, and quality assurance processes, along with knowledge of industry best practices in manufacturing, production, and quality management.
Committed to process optimization and continuous improvement by staying up-to-date with industry trends, SAP and MES updates, and regulatory changes while actively seeking opportunities to improve manufacturing processes, streamline operations, and enhance system efficiency. Apply analytical and problem-solving skills with lean techniques and modern manufacturing processes, including data analytics, AI, visualization, and error proofing.
Skilled in systems integration and architecture, ensuring the compatibility, integration, interoperability, stability, scalability, and usability of products and services proposed as standards to ensure an integrated architecture across interdependent technologies. Extracted insights from key shop floor manufacturing systems like MES, SCADA, IoT devices, and PLCs while leveraging analytical tools to pinpoint and implement improvements across various operational processes.
Demonstrated expertise in regulatory compliance and industry standards, including familiarity with GxP, FDA regulations, 21 CFR Part 11, and other relevant industry standards. Possesing solid understanding of the Life Sciences industry, specifically the challenges and regulatory considerations related to batch release, manufacturing, and quality assurance processes, along with knowledge of industry best practices in manufacturing, production, and quality management.
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