Kiran Kumar M

• Visit plant daily basis in a production area, and identify the hazard.
• Reduced incident rates through the implementation of comprehensive safety training programs for employees.
• Developed targeted safety campaigns aimed at reducing specific types of incidents within the organization.
• Conducted thorough risk assessments for new projects, ensuring all necessary precautions were taken to maintain worker safety.
• Provide SDS in hazard working area.
• Enhanced workplace safety by conducting regular inspections and identifying potential hazards.
• Improved employee compliance with safety regulations by developing and implementing clear policies and procedures.
• Observed packing operations to verify conformance to specifications.
• Give a tool box training in employ's in a production area.
• Keep a hazard signboards in a plant area and hazard areas.
• observed all hot work an cold work,confine space, hight work,excavation work.
• Maintain all workpermits into the working time.
• Check all safety equipments expiry and undated labels.
• Maintain all PPE'S to the plant area.

• Co-ordination and execution of Downstream manufacturing of API up to 3 KL in a GMP system.
• Arranging of raw and packing materials, plant and utilities required for production of various products.
  
  • Document up keeping: review of Batch Records and equipments record.
  
  • Identify training needs of production operators and helpers and arrange same.
  
  Responsible for the documentation of production activity.
  
  • Reconciliation of packing and raw materials used for production.
  
  • Making sure that the production facilities are clean and when appropriate disinfected.
  
  • Making sure that the necessary calibrations are performed and record kept.
  
  • Making sure that the premises and equipment are maintained and records kept.
  
  • Providing safety watch out for all the operations in the manufacturing area and coordinating equipment maintenance activities.
  
  • Maintaining for cleaning activity in shop floors and pharma area as per GMP activity's.
  Preparation and review of manufacturing documents including batch records, SOP and cleaning checklist.
• Maintained accurate documentation of production data, enabling informed decision-making for process improvements.
• Implemented safety protocols and conducted regular audits, achieving a reduction in workplace accidents and incidents.
• Managed inventory levels effectively to ensure availability of raw materials and minimize stock discrepancies.
• Oversaw loading and unloading of packages in warehouse.
• Supervised ongoing daily production phases.

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• same as above