Dananjayan Reddy

Experience

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  Malladi Drugs and Pharmaceuticals Limited

  Sept 1990 - Jun 2008

  Sr. Officer Production

   Administered Shop Floor production activities, maintained production records and monitored clean room area as per guidelines and regulatory requirements. Planned preventive maintenance of machines to avoid breakdowns and smooth production processes. Prepared internal quality and safety audits. Monitored purified water as per norms and requirement. Conducted training sessions for the team from as and when required. Maintained quality standards cGMP, USFDA and ISO 9001-2000 and all other related documents and records. Ensured execution of Validation as per protocols. Supervised raw material requirement, availability and usage of raw material in the process at regular intervals. Show less

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  Embio Limited

  Jul 2008 - Sept 2012

  Sr. Manager Production

   Administered complete production activities of the complex having three blocks. Monitored Production planning, Budgeting, and review of production schedule as per marketing requirement, cost control and timely submission of Status reports. Ensured preventive maintenance scheduled activities for production equipment optimum utilization and to avoid untimely breakdowns. Supervised and maintained production records as per the regulatory requirements and execution of Validation as per protocols. Managed clean room area as per regulatory requirement and monitored purified water as per requirement. Interacted with Consultants and Vendors and coordinated with QA and QC for Validation. Prepared Capex Budgets and implementation of small size jobs  Executed cost savings and energy savings techniques / measures; modified to achieve substantial reduction in O & M expenditures. Imparted training to subordinates on smooth operations of the equipment, process knowledge, how to handle maintenance & breakdowns and cost saving exercises. Assigned URS to any new requirement for project. Prepared for internal & external audits; carried out period internal Quality & Safety Audits and compliance. Ensured adherence to quality standards cGMP, USFDA and ISO 9001-2000 and maintenance of documents. Complied with IPC & FP as per QA-QC Specifications and documentation: DQ, IQ, OQ, PQ, Validations, etc. Gathered raw material requirement and maintained stock for the use of material in Process. Show less

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  BVM pharma Limited

  Oct 2012 - Sept 2014

  Sr. Manager Production

   Managed production designing, utility, ETP requirements and overall project work activities. Reviewed and negotiated on quotations, prepared and obtained approvals for all documents such as construction, statutory, machinery,  Monitored and coordinated with stores and purchase for adequate inventory to ensure hassle free production and timely execution of orders. Achieved all production targets and complied with all regulatory norms within budgeted norms in the field of API/Bulk drug. Identified performance issues, developed & implemented improvement plans for better growth and results. Working in close coordination with various teams/department ensuring meeting targets and deadlines. Show less

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  Piramal Enterprises Limited

  Dec 2015 - now

  Production Manager

   Monitored Production planning, Budgeting, and review of production schedule as per marketing requirement, cost control and timely submission of Status reports. Ensured preventive maintenance scheduled activities for production equipment optimum utilization and to avoid untimely breakdowns. Supervised and maintained production records as per the regulatory requirements and execution of Validation as per protocols. Managed clean room area as per regulatory requirement and monitored purified water as per requirement. Interacted with Consultants and Vendors and coordinated with QA and QC for Validation. Prepared Capex Budgets and implementation of small size jobs  Executed cost savings and energy savings techniques / measures; modified to achieve substantial reduction in O & M expenditures. Imparted training to subordinates on smooth operations of the equipment, process knowledge, how to handle maintenance & breakdowns and cost saving exercises. Assigned URS to any new requirement for project. Prepared for internal & external audits; carried out period internal Quality & Safety Audits and compliance. Ensured adherence to quality standards cGMP, USFDA and ISO 9001-2000 and maintenance of documents. Complied with IPC & FP as per QA-QC Specifications and documentation: DQ, IQ, OQ, PQ, Validations, etc. Show less