Omkar Kamble Email and Phone Number

Key responsibilities- Developing and managing demand planning processes in SAP to accurately forecast clinical supply needs. This includes creating independent Clinical Finished Goods (CFG) demand and managing dependent demand linked to the Bill of Materials (BoM) structure of end products.- Managing demand directly related to Bill of Materials (BoM) structure of end products, creating dependent demand for primary packaging (PP), drug products (DP), drug substances (DS), packaging materials, and labels.- Advising on the optimal supply strategy, performing risk management to mitigate study risks and ensure supply continuity.- Lead supply planning process in Kinaxis Rapid Response by planning and monitoring the end-to-end clinical supply, adapting the supply plan to accommodate constraints such as IMPD updates and product expiry.- Developing and executing comprehensive distribution plans to ensure timely and efficient delivery of clinical supplies to all trial sites. Coordinating the logistics of supply shipment in line with randomization schemes and anticipated site demand.- Implementing inventory planning strategies to ensure the availability of clinical supplies across multiple locations, including sites, hubs/depots, and warehouses. Maintaining safety stock levels to mitigate uncertainties during trials, ensuring uninterrupted supply and accommodating unforeseen demand variations.

Quality Improvement for Machining Rejection Control through Process and Supply Chain Improvement for automobile differential

Developed and implemented Key Performance Indicators (KPIs) and Key Result Areas (KRAs) across the entire organization to monitor and enhance growth and operational excellence in both internal and external landscapes.

Collaborated with senior members for deep functional insights, optimized business processes. Utilized Alteryx Designer for data efficiency, Qlik Sense for data-driven decisions. Automated carbon footprint data extraction, optimizing distribution with sustainability focus. Improved inventory oversight for CFGs through IRT-based automation. Conducted an in-depth analysis of shipment patterns vis-à-vis patient recruitment dynamics proved pivotal in identifying key drivers behind the increased shipment volumes. Analysed shipment and consumption rates, extracted actionable insights that translated into substantial reductions in waste and shipment costs.

Client Relationship Management: Successfully established and nurtured strong client partnerships through regular meetings and persuasive communication. This approach resulted in increased purchase orders and enhanced customer satisfaction.Team Leadership: Led a dedicated team of 6 engineers, overseeing knowledge transfer and training initiatives for Graduate Engineer Trainees (GETs). Facilitated seamless communication by sharing daily breakdown and installation reports, thereby fulfilling commitments to stakeholders.Project Execution: Demonstrated exemplary project management skills by executing projects within established timelines and without cost implications. Ensured adherence to qualification tests and procedures, while providing thorough instrument training and on-site trial runs.Cross-Functional Collaboration: Collaborated effectively with cross-functional teams to manage backend tasks, including quotation creation and invoice generation. Assisted the sales team in lead generation and met business technology demands.

Technical Proficiency: Expertly operated, diagnosed, and rectified a range of analytical equipment crucial to the Pharmaceutical and Chemical industries. Ensured equipment functionality and accuracy, contributing to streamlined operations and high-quality results.Issue Resolution: Responded to customer complaints, promptly attended breakdown calls, and effectively resolved issues within defined timeframes. Maintained a high level of customer satisfaction and minimized disruptions.Regulatory Compliance: Conducted Qualifications (IQ/QO/PQ) and calibrations of Analytical instruments in alignment with ISO standards, USP/EP pharmaceutical regulatory guidelines, and 21CFR PART 11 regulations. Maintained impeccable document credibility.Quality Assurance: Administered comprehensive quality control checks such as Factory Acceptance Tests (FAT) and Site Acceptance Tests (SAT). Ensured equipment reliability, minimized downtime, and reduced defects, thereby enhancing overall quality assurance.

performing maintenance and troubleshooting for various instruments at crude distillation unit