Experience

JB

• India
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Senior Production Manager

  • Jun 2022 - Present

  Continuous Improvement · Team Leadership · Production Management · Production Planning · Manufacturing · Process Improvement · Team Management

• Production Manager

  • Aug 2020 - Jun 2022

   Working as area leader and responsible for Granulation, Compression, Coating, Drilling, Inspection, Printing Area and Documentation. Preparation of Weekly and Monthly production planning module. Floor men power planning and utilization, Production Planning. Budget Handling and maintaining (Revenue/capex) Procure equipment's, machinery and other facilities required for the manufacturing of products. Preparation of documentation like SOP, Area Qualification, URS, Equipment qualification like IQ, OQ, PQ etc Co-ordination with Store for RM dispensing, QC for In process sample testing, Engg Department for Utility-HVAC and Utility Qualification from production Department. Ensure timely receipt of Raw Materials and Packing Materials in coordination with Purchase Department. Generating various reports/presentations on daily and monthly basis and presenting them to higher management. Looked after the entire gamut of operations encompassing CAPA, change controls and deviations, Complaints, Investigation in Caliber QMS System. To ensure that Preventive Maintenance of all critical equipment's are carried out as per Preventive Maintenance schedule and to maintain the equipment's and building in good condition. Responsible to company the requirements of statutory audits, internal audits and tax audits etc.

• Assistant Production Manager

  • Jun 2016 - Jul 2020

  Handling Production Planning, Handling Electronic Batch Record Management System, Maintaining Daily Production Records, Scale up and new product introduction.



Teva Pharmaceuticals

• Israel
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Production Executive

  • Apr 2015 - May 2016

   Working for Green Field project for the site in for Pharma Production and ensured adherence to Production compliances. Overseeing production related tasks including planning and control  Setting up production targets and achieve the same within time and cost parameters. Optimising man & machine utilisation to achieve pre-set production targets. Developing new process concepts for production optimization, yield improvement. Well Versed with software’s like SAP / LMS/ TRACKWISE/ LIMS/ GLORYA  Looked after the entire gamut of operations encompassing CAPA, change controls and deviations, Complaints, Investigation in Track wise software (QMS). Corporate standard implementation at site. GAP assessment.



RPG Life Sciences Ltd.

• India
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Sr.Executive

  • Aug 2014 - Apr 2015

   Review of ANDA products executed batch Packing records and online review of executed BPRs. I have experience of prepare SOP, Qualification protocol and its execution. I have make weekly and monthly planning for packing department. I have experience of packing and handling manpower on packing line. Handling of Following equipment’s like • Blister Packing Machine - Romaco & Elmech 3020 Machine, • Track & Trace System (Verif – I Secondary & Tertiary System, • Bulk Packing Machine • Shrink Pack Machine (Make – Ramesh Eng.)• Blister Inspection System (Make – Jekson, Model – BIS NXG)• Inkjet Printer (Make – Image India)• Label Printing Machine



Famy Care Ltd., Mumbai

• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Sr. Production Officer

  • Apr 2012 - Jul 2014

  Manufacturing Activity:  Involved in different trial batches like Optimum Scale up Batch, Exhibit Bathes, Pre-validation and Commercial Batches on various county requirements. Involved in different process of solid drug dosage production development cycle like Dispensing of active and non-active raw materials, Sifting, Granulation, Blending, Milling, Tablet compression, Looking after trouble shooting, Stage wise yield calculation, Label & weigh finished products as per SOP’s. Supervision of miscellaneous activities like gowning procedure in processing area, deactivation of used gowning and waste generated during manufacturing process, disinfectant solution preparation, and movement of in process materials, issuance, receipt and inspection of FBP bag, sieve and screens. Maintenance of die-punch sets and inspection of new tooling received along with documentation. Review of ANDA products executed batch records and online review of executed BMRs

• Production Officer

  • Jan 2011 - Mar 2012

  Documents & Audit Preparation: • Preparation of new BMR and BPR as per TTD.• Handling of change control, deviation, incident report and CAPA.• Preparation of SOPs for new equipment’s and revision of SOP as per scheduled revision.• Maintain various Documents like Punch records, FBD bag record, Sieve and Screen record, Machine log books, Temperature& Humidity Records, Differential air pressure records, Digital balance checking, Area cleaning records etc.