Amit Sharma is seeking a position that allows career growth and challenges. He has over 10 years of experience in pharmaceutical manufacturing in roles of increasing responsibility. His experience includes manufacturing oral solid and liquid dosage forms, topical preparations, sterile products, and aerosols. Key responsibilities have included production planning, supervising production operations, equipment maintenance, process validation, and implementing new systems. Notable projects include technology transfers and increasing batch sizes. He holds a B.Pharm and MBA and is proficient in English, Hindi, and various computer programs and manufacturing systems.

1. -
Amit Sharma
Mob No:- +91-9410901630
Email/Skype Id.: amitpharmamatrix@gmail.com
Objective: Self drivenprofessional,havingCareerfull of challenges,growthandempowerment. andbe a part of team
that dynamicallyworkstowardsgrowthof organization
Permanent Address :
H.No.-5, Chandra
villa,Devlok Colony,
Shimla Road,
Dehradun,UK-248002
Personal Details :
Sex
Male
Marital Status
Married with 2 sons
Date ofBirth
30-Nov.-1981
Nationality
Indian
Father’s Name
Mr. K.C. SHARMA
Languages Known
English, Hindi
Hobbies
Meditation/Listening
music(Hindi/English)
Strengths
Team Leader, Team
Player, and Handling
critical situation
strategically.
EDUCATION:
1-B.PHARM in 2003
SGRRITS, D,Dun
2-MBA(Fin. & Mrktg)
in 2008(DE)-SMU
3- 10+2 from CBSE
in1999. SGRR school.
PASSPORT: YES
Employment Summary:
Organization’s Name Designation Duration
G.S.PharmbutorPvt.Ltd.(Win–Medicare)–
WHO,ISO-13485,22000,9001-2008
Dy. Manager-
Production
Working Since Dec-25-2011
Simpex Pharma Pvt. Ltd.(Corel med-
RUSSIA)-WHO-GENEVA,UKRAINE
Sr. Executive-
Production
Jan.-3-2010 to Dec.-20-2011
Capsugel Healtcare Ltd.(Pfizer)- US-
MNC – WHO 9001-2005
Process
Engineer-Mfg.
Dec.-3-2008 to Dec-13-2009
Baxter India Pvt. Ltd- US- MNC – LSP
approval,WHO,ISO-13485,UGANDA
Mfg. Associate Sep.-12-2007 to Nov.-30-2008
Windlas Biotech & healthcare Ltd, WHO,
ISO-9000, USFDA, UKRAINE
Asst. Chemist Dec.-14-2003 to Dec.-30-2006
Skill Set:
Leadership, Action oriented,
Communication
Capable of working well under pressure within a team
environment, A ‘Do what it takes ‘mindset with possible
attitude, . Quick learner and easy adaptability to new
methods and system .Good listener.
Office Tool, Operating
System, Editing Tool
Microsoft Office 2000,2003, ERP System, Windows
98/Xp/7,8, Photoshop 7.0
Team co ordination,
Inventory & Mfg. Skills
Coordinates and manages pharmaceutical product
manufacturing (Planning-Shop floor).
Responsible formaintainingadequate inventoriesof
productto meetmanufacturingneeds.Where
necessaryleadsteamresponsible formanufacturing
projects
AUDIT Faces WHO Audit, EHS Audit( ISO 14001), MOH Audit.,
Internal, Corporate Audits, WHO Geneva audit, ISO-
9001-2008, ISO-22000, ISO-13485,USFDA, UKRAINE
AUDIT hosting team
member
WHO Audit, MOH Audit., Internal, Corporate Audits,
WHO Geneva audit, ISO-9001-2008, ISO-22000, ISO-
13485,UKRAINE
INDIAN FDA give
Approval for Mfg.
Small volume parenterals,Tablets,Capsules,Liquid
Orals,Dry Syrupsand Ointments. (Biological and Non
Biological Products)
Emphasizing skills Supervisingplantoperations. Investigatingand
troubleshootingplant/processproblems. Scheduling
and coordinatingworktotightdeadlinesandwithin
financial budgets. Ensuringthat equipmentworks
to itsspecificationandtoappropriate capacities.
Assessingsafetyandenvironmental issues.
Liaisingwithinstallation/projectengineersand
specialists. Ensuringsafe workingconditionsand
compliance with environment, healthandsafety.

2. JOB PROFILE TILL TODAY( MANUFACTURING) :
1. Manufacturing & packing of Oral solid/liquid dosage form-Tabs, Caps, Dry Syrups &Oral Fluids
( 5 years)
2. Manufacturing & packing Topical preparations-External Liquid, Ointments and creams.(2 years)
3. Manufacturing, filling, sterilization & packing of sterile preparation - SVP/LVP.(3+1 years)
4. Manufacturing, filling, gasing, leak test and packing of Aerosols.(1 year)
JOB RESPONSIBILITYWITH ABOVE PROFILE
5. Responsible for preparing Production plans as per monthly plans received.
6. Responsible for job allocation of Supervisors section wise for supervising all unit operations.
7. Responsible for indent of change parts for the Production equipments and advising Engineering
department for procuring spares time to time.
8. Responsible for coordinating with Warehouse, Quality control and Quality Assurance for daily
follow ups for material, analysis and documentation respectively.
9. To ensure that the products are produced and stored according to the appropriate
documentation in order to obtain the required quality.
10.To approve the instructions relating t o Production operations including the in-process controls
and to ensure their strict implementation.
11.To ensure that the Production Records are evaluated and signed by a designated person before
they are made available to the QA Department.
12.To check the maintenance of the department, premises and equipment.
13.To do and ensure the appropriate process validations and calibrations of control equipments.
are performed and recorded and the reports made available.
14.Implement New System and Technologies as required.May train new staff members in process
and procedures. Work with project team members to analyze their requirements
Project Undertaken
A - IN CAPSUGEL HEALTHCARELTD
1. Technology transfer – Value in Process(recuperation of Hard gelatin capsule shells) and systemup
gradation - 15 days – CHINA –SUZHOU Plant( Successfully Implemented in India within Time
framed-3 months ).
2. Machine Mechanic – Gelatin Tanks washing and cleaning M/C commissioning Mr. Gary from
Belgium Plant
3. Leadership Project- Gelatin Batch Manufacturing process training to employees, who don’t have
exposure to SCADA( 1 Month).
B - In BAXTER INDIA PVT.LTD.
1. PRODUCTIVITYIMPROVEMENT: Part ofTeam to increase Dialysis soln. Ringer lactate soln. Batch size
from 25KL to 30 KL. Successful trial batches taken & implementation.
C - In ATLAS LABS. AND PHARMACEUTICALS:
1. MACHINE COMMISIONING: Tablet section, Ointment section, Capsule section with QA dept.

3. TRAININGS
1- EHS
2- Process flow- From URS to User end -Capsugel
3- GMP Aspects ( CALGS)
4- QA Aspect ( CALGS)
5- Leadership in Action
Achievements
1-Successful implementation of Tech. Transfer from Capsugel – Suzhou – China to Capsugel- India Plant of Empty
Hard Gelatin capsule Recuperation.
2-Represents Production during WHO- GENEVA pre-audit and clear that audit with 01 minor point in SIMPEX
Pharma Pvt. Ltd.(COREL –MED).
3-On the go, from project to production, first taking pilot batches and then final production.
4- Got man of the match in Cricket tournament final match of 5 institutes and we won that Trophy
Declaration: I hereby to confirm that all Information given in my Resume are true and Authenticate through
my Knowledge.
THANKING YOU
DATED 10/07/15
PLACE: Rudrapur .Uttarankhand (AMIT SHARMA)