Prabhat Kumar Mishra

Background

About Prabhat Kumar Mishra

Professional having approx 18 years of pharmaceutical manufacturing industry experience across diverse formulations like Tablets/ Pellets/capsules/Ointment/Liquid Orals//Inhalers. My convincing power and out of the box thinking are key strengths that have seen me through tough situations. I bring with me exceptional interpersonal and influencing skills enabling success in a complex and matrix organization structure with multiple stakeholders. I am deft at monitoring performance, analyzing status & progress reports and manage complex business challenges with strong work-ethics, interpersonal communication, relationship management and analytical skills. Adept in the implementation of techniques for improving operational efficiency and achieving cost savings. Areas of excellence include execution of Green field projects, Technical finalization of Equipment's, Palletization & Tablet manufacturing processes, Yield and process improvements in the fields of Pharmaceutical Oral Solid Dosage forms manufacturing. Sound knowledge & exposure of Handling regulatory audits, Preparation of Audit responses & compliance reports. Updates on current Regulatory & Technical requirements. Ensuring compliance of the Quality Management Systems like Change Control, Deviation, Market Complaints, OOS / OOT and ensuring the effectiveness of the systems in manufacturing environment. Manufacturing planning, process optimization, process standardization, trouble shooting and problem solving. Continuously achieving higher levels of productivity and quality norms by optimizing the available resources — Man, Material and Machine. ensure maintenance and up-keep of production, support systems and facility. Plan and coordinate all activities leading to timely delivery of new product launches/FTF launch products and site transfer products. Preparation & implementation of Manufacturing/Packing plans at shopfloor by ensuring stringent adherence to quality standards. Planning and executing validation and qualification activities. Liaising with Quality Control, Quality Assurance, Warehouse, SCM, PPMC, Demand planners and Engineering department for cGMP & its implementation as well as providing support and guidance in technical and cGMP related matters. I ensure regulatory compliances on shopfloor & execute self-inspection for capacity up-gradation and other routine activities within stipulated time and cost.