To,

RESUME

Mr. SUBRAT KUMAR SAHU

Bachelor of Pharmacy (FDA Approval in Tablet Manufacturing)

Contact No – +917*********

Email – actthl@r.postjobfree.com

CAREER OBJECTIVE

Aiming to be associated with a progressive organization that gives me scope to upgrade knowledge and management skills in accordance with the latest trends and to be a part of a team that works towards the growth of the organization and gain satisfaction thereof.

EXPERIENCE & DESIGNATION:

A handful experience of about 8 years in Manufacturing & Packaging of solid oral. 1. Now working as an Assistant Manager Production in Pharma Giant SANOFI INDIA LIMITED GOA site, since 2011 to till date.

2. Previously associated with GLENMARK GENERICCS LIMITED, GOA as a officer Production for about 1 year.

3. Have worked for IPCA Lab Ltd. as officer production for 2.5 years.

AREA OF EXPOSURE

Manufacturing & Packaging of solid oral (i.e. Granulation, Compression, Coating, Encapsulation & Packaging operations)

ACADEMIC PROFILE

1. HSC from BSE, Bhubaneswar-Odisha in 2002 with 70.5% marks. 2. CHSE from Bhubaneswar-Odisha in the year 2004 with 61% marks. 3. Bachelor of Pharmacy from BPUT, Rourkela- Odisha in the year 2008 with 75% marks. 4. Get certification from Cambridge University, London-UK for IELTS in the year 2015 with Band Score R-6/W-6.5/L-6 & S-6.

JOB DESCRIPTION:

1. Manpower handling (A group of 16 executives & 52 Operators) and monitoring daily production activities.

2. Coordinating with Warehouse, QA, QC for the material availability, its release & scheduling the batch production to meet the market requirements. 3. Preparation of shift schedules for Executives & operators & monitoring their performance through Appraisal system quarterly.

4. Responsible for Good Quality products with standard output in individual shift and cent percent adherence to cGMP, without any FDA violations. 5. Conduct training on cGMP, GDP, New & revised SOPs, CAPA to Deviations to the shop floor personnel.

6. Troubleshooting of problems arises during the process i.e. in granulation, compression, coating & packaging.

7. Preparation & review of the documents like SOPs, BMR, MFR, Process Validation Protocol, and Process Validation Report.

8. Actively involved in the FAT, IQ, OQ, PQ of the new equipment. 9. Responsible for the Execution of Process validation. 10. Assist to product development team for the new product validation & site transfer. 11. Prime responsible for implementation of TPM, LEAN (SMED, VM, VSM) a MANAGEMENT tool for all type of industries that help a lot for survival of industries even at the time of crisis.

(A tool for producing product with least cost & high quality that’s reduced the NVA cost. Trouble shooting during the processes i.e Granulation, compression & coating . 12. Responsible for the OEE & Pant Cycle Time management (the tool that facilitates the JIT production & makes a PULL market for products).

13. Revision of ROUTING of products for COGs improvement. 14. Involved in Yield Improvement of costly products. 15. Assessment of risk factor related to workplace safety & preparation of the Work Place Risk Assessment & Process Risk Assessment.

16. Conducting shop floor training on industrial Safety & PPE requirement. 17. Effective Implementation of 5-S program in shop floor. 18. Responsible for maintaining the Machine tools/spares, accessories & daily consumables. 19. Handling of the online Change control & deviation system like GIMC & PHENIX 20. Trained & Certified First Aider.

ACHIEVEMENT (SUCCESSFUL PROJECTS WORKS):

1. Industrial Innovation Award for the LEAN initiative in the coating process validation i.e increased in lot size to reduce 33% of process time.

2. Reduction of changeover time in compression by 25% with 50% reduction in man hours in order to meet the market requirement & timely delivery of products in to market by applying the SMED tool, so to create a PULLING business & JIT production.

3. Revalidation of cleaning process by reducing the cleaning cycles by 50% (WIP) so a huge saving in the water consumption with new cleaning validation in place.

4. Introduction & validation of alternate suppliers, for a numbers of API & Excipients to saves cost pertaining to imported raw materials approx. 10 million per years.

5. Long Campaign size study for the large volume products & increased batch size to minimize the QC analysis costs by 1 million per year.

6. Validation in multiple machines for 100% percent capacity utilization & a perfect LRP.

7. TPM workshop in Blister Pack machine.

8. VSM of existing product to decrease its processing time.

AUDITS FACED

MHRA, USFDA, ANVISA, TGA, WHO & Local FDA

COMPUTERS PROFICIENCY

Exposure to MS-office Tools.

A wide exposure of SAP UNTITY & SAP ATHENA system used in pharma industries.

PERSONAL DETAILS

Father’s Name --- Late Sri Dhaneswar Sahu

Mothers Name--- Smt. Lopamudra Sahu

Marital Status---Married

Date of Birth---09th July 1987

Nationality---Indian

Language Proficiency--- English, Hindi & Oriya

DECLARATION

I do hereby declare that all the above-mentioned information are true and complete to the best of my knowledge and belief and nothing has been concealed herein. Date:

Place:

SUBRAT K. SAHU

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