Tapan Palai

About Tapan Palai

Sr.Executive-Production having more than 8.7years of experience on Solid Oral Dosage forms.

Experience

1. Sr Executive-production

   Sandoz

   Aug 2011 — Present · MUMBAI, IN

   Planning & Execution of Production Schedule. Managing whole responsibilities of manufacturing as a shift-in-charge. To plan, organize and co-ordinate all activities related to manufacturing of tablets and capsules. Responsible for cGMP compliance and validation including execution review of SMF, VMP, Protocols, Cleaning Validation, BMR, SOP’s etc. To ensure cGMP compliance/audits and Validations activities. Responsible for monthly production scheduling in coordination with SCM as well as raw material dispensing planning according to priority & availability of RMs. Coordination with Linked Departments like QA, QC, WH, Tech Services, Engineering, Projects, ETP & HR. Involved in preparation, revision & display of all required SOPs for the department. Reviewing routine calibration/environment monitoring practices & shop Floor Documents. Man power planning (technicians & officers) & deployment as per requirement. Arranging Training Programmes for subordinates, technicians & workers. Periodic verification of all equipments of Granulation, compression, coating & capsule filling. Verification of all civil/electrical works inside the manufacturing area & taking hand over of all new areas and equipments from project department. Verification of calibration & performance tests of all new equipments. Involved in equipment validation in preparation & execution of qualification protocols & reports like URS, FAT, DQ, IQ, OQ & PQ). Involved in Exhibit & process validation of new products. Handling of deviations, change controls and CAPA as per the system.

Education

• Berhampur University

  B.Pharma

  2001 — 2005

Skills

• Pharmaceutical Industry
• Sop
•  Operating Systems: Windows-98, Xp & Ms. Office.
• Regulatory Affairs
• Pharmaceutics
• Gmp