Pravin Panmand

Experience

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  Fresenius Kabi

  Jul 2013 - Jan 2015

  Officer

   Manufacturing paracetamol infusion in 50ml, 100ml and Compound amino acid (aminowel 5%) 250ml Glass bottle using nitrogen purging method .Also, lifesaving intravenous infusion large volume parenteral in Poly ethylene bottles using BFS technology. Supervise manufacturing activity of equipment preparation & sterilization batch filtration storage in allocated shift and ensure process adherence as per SOPs. Verified that all process control parameter were being documented and followed at all time. Co-ordinate with production planning and availability, Engineering service quality assurance & quality control for smooth functioning of the process. Involve in qualification & validation activity. Show less

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  Centaur Pharmaceuticals Pvt. Ltd.

  Jan 2015 - Mar 2016

  Officer

  Weekly and monthly planning and execution of production batches. To ensure availability of technical documents at MFG site. Review of Batch Manufacturing Record (BMR) and Batch Packaging Record (BPR). To investigate market complaint/Depot inspection to resolve critical issues. To implement calibration and validation activities at MFG site. To prepare plan & monthly reports. Monthly physical stock checking at concerned location. Routine co-ordination with PPIC, CQA, RA, SCM etc. Assist in production planning and execution of batches dispensing of raw material as per Coordinating through interaction with (Research and Development Dept., Manufacturing Dept., Quality Control Dept., Quality Assurance Dept., Packing dept.) Show less

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  Sandoz India Pvt Ltd

  Mar 2016 - Sept 2022

  Executive

  Preparation of the training calendar yearly for annual refresher trainings.• Training Need Identification of all employees after discussion with all HODs & approval• Interact with Corporate & Global QA / Training for QMS training• Organize External Training & Webinars for employees.Preparation review and execution of Training effectiveness check at Site.• Support implementation & Resolve issues w.r.t. LMS.• Preparation of Questionnaire for the Technical Training Module.• Provide the Training to the BOAT.• Monthly report compilations and submission on time.• Prepare and update Quality review meeting report and present site meeting.• Line Clearance Effectiveness Check certification.• External Training Updating in LMS.• Review Training Files and Other System Documents and provide support during the audits for all FDF location. Management and control of revision of SOP Dealing with change control, implementation ESOP management, technical lead.  Handling of Change control, deviation, quality event. Review and approval of QMS related documents. Deviation management and CAPA implementation. Show less

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  Novartis

  Sept 2022 - now

  GxP Training & Learning Operation Expert - Global Quality / QMS Novartis

  Training Process Standardization, Audit Support, LMS Governance and incident Management, Issue Management, QMS, TM Review, Training KPI Monitoring, Quality Checks, Employee Onboarding.• Development of the Training Effectiveness methodologies for various trainings carried across NVTS.• Reporting and Tracking of Business Training performance through agreed KPIs and KQIs.• Collaboration with different stakeholders for Skill development and understanding the Site Training Scenario.• Implementation of Digitized solution across Novartis for Training management and support as a Training service. Show less