Summary
Overview
Work History
Education
Skills
Accomplishments
Personal Information
Roles And Responsibilities
Disclaimer
Languages
Timeline
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Deepak Kumar  Jena

Deepak Kumar Jena

Pharmaceuticals
Vapi,Gujarat

Summary

To pursue a challenging, dynamic, responsible and rewarding career to apply my skills in a position for career growth in industry and to work in the field where my professional expertise, skills and enthusiasm will have application and improvement

Overview

18
18
years of professional experience

Work History

Deputy Manager

USV PVT Limited
Daman
03.2010 - Current

Officer

Macleod pharmaceuticals Limited
06.2008 - 03.2010

Officer

Litaka pharmaceuticals Ltd.
04.2006 - 06.2008

Education

Bachelor Of Pharmacy - Pharmaceuticals Science

IGIPS
Bhubaneswar
08.2005

Master Diploma In Production Management - Pharmaceuticals Science

IPER
Pune
10.2009

Skills

Performance improvements

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Accomplishments

  • Achieve the Highest out put for the plant without any Non compliances.
  • Maximum manpower developed in all section like Granulation, compression, and Coating.
  • SOP changes as per the requirements in kaizen idea.
  • Maximum OEM training conducted for training of Technicians and supervisors.
  • Daily Audit schedule removed the fear for any time Regulatory audit.
  • Successful in all audit like USFDA, MHRA, WHO without any major and critical observation.
  • Supervised team of 110 members including staff and Technicians .
  • Documented and resolved BMR which leads to increase in output without any noncompliance.
  • Ranked 816 in OJEE medical entrance exam in the year 2000.
  • Reckonized from Makenzie consultant for providing maximum no of kaizen idea and it's implementation in USV PVT Limited.

Personal Information

  • Father's Name: Kunja Bihari jena
  • Mother's Name: Monorama jena
  • Date of Birth: 05/22/80
  • Gender: Male
  • Nationality: Indian
  • Marital Status: Married

Roles And Responsibilities

  • Monitoring the Shop Floor activities handling equipments like, (RMG, FBP, Wruster coating(Glatt), Co-mill, Ball mill, OGB, Drum Blender, Compression (Sejong HRC 49Stn, C-300 Compn machine, Cadmach) and Coating (Sejong) Capsule filling Machine (AF-90T), Imprinting machine, Viswill inspection machine.
  • Responsible for Online Review of BMR through supervisors.
  • Execution of Process Validation batches in coordination with QA and QC Departments.
  • To review the day to day cleaning activity in Departments and Training of Housekeeping person.
  • To review the punch utilization record, FBP bag, sieve, screen, inventory and utilization record.
  • To participate in cost reduction process in coordination with EHS Department.
  • To maintain yield record for all products.
  • Issuance of Work Orders to maintenance Department for breakdowns and Preventive Maintenance.
  • Prepare weekly plan and discuss with subordinates for its effectiveness.
  • Review of existing BMR and correct if needed as per routine practice.
  • Impart GMP, GDP training to all Technicians.
  • Impart Regulatory awareness training to all Technicians.
  • Responsible for effective utilization of manpower, Machine, Material and methods.
  • Coordinate with staff for work assignments and continuous improvements as per regulatory requirements.
  • To plan the production schedule by preparing Production plan through 90 days plan.
  • To overview the work allocated among operators on a daily basis on machines in shifts and prepares shift schedules.
  • To supervise the production activities on a day-to-day basis and guiding the operators and troubleshooting for smooth operation of machines/processes.
  • To co-ordinate and follow up with other department like Purchase department, warehouse, QC, QA for timely delivery of semifinished product to packing department through 90 days advance planning.
  • Promote team work by providing support and training to all Technicians.
  • Actively participate in Continuous Improvement Projects (CIP).
  • Responsible for manpower requirements in production area in coordination with HR department as needed.
  • Responsible for cGMP implementation through training.
  • Performing Safety Audits and Daily Audit in Departments.
  • Responsible for execution of DQ, IQ, OQ, PQ.
  • Prepare SOP, and filling of change control and Investigation reports.
  • Certified investigator in USV for investigation of OOS Deviation, OOT.

Disclaimer

I hereby declare that the above mentioned information is true up to my knowledge and I bear responsibility for the correctness for the above mentioned particulars.

Languages

Hindi
Bilingual or Proficient (C2)
English
Upper intermediate (B2)
Oriya
Advanced (C1)
Gujarat
Intermediate (B1)

Timeline

Deputy Manager

USV PVT Limited
03.2010 - Current

Officer

Macleod pharmaceuticals Limited
06.2008 - 03.2010

Officer

Litaka pharmaceuticals Ltd.
04.2006 - 06.2008

Bachelor Of Pharmacy - Pharmaceuticals Science

IGIPS

Master Diploma In Production Management - Pharmaceuticals Science

IPER
Deepak Kumar JenaPharmaceuticals