1. Amit Sharma
Mob No:- +91-9410901630
Email/Skype Id.: amitpharmamatrix@gmail.com
Objective: Self driven professional, having Career full of challenges, growth and empowerment. and be a part of team
that dynamically works towards growth of 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 of Birth
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
Persuing M.pharm
last sem.
2-MBA(Fin. & Mrktg)
in 2008(DE)-SMU
3- 10+2 from CBSE
Employment Summary:
Organization’s Name Designation Duration
Pil pharma pvt ltd( beta lactum)
HARIDWAR
(Tabs,caps & dry syrup).
.GS.PharmbutorPvt.Ltd.(Win–Medicare)
–WHO,ISO-13485,22000,9001-2008
( Ointment/External
liquid/Tablets )-Betadine , dhepamerzz etc.
Mgr
production
Dy.
Manager-Prod
uction
01 sep-2015 to till date
Dec-25-2011 to 30-aug.2015
Simpex Pharma Pvt. Ltd.(Corel
med-RUSSIA)-WHO-GENEVA,UKRAIN
E
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 for maintaining adequate inventories of
product to meet manufacturing needs. Where
necessary leads team responsible for manufacturing
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
2. in1999. SGRR school.
PASSPORT: YES
CTC – 8.5 Lac
INDIAN FDA give
Approval for Mfg.
Small volume parenterals, Tablets, Capsules,Liquid
Orals, Dry Syrups and Ointments. (Biological and Non
Biological Products)
Emphasizing skills Supervising plant operations. Investigating and
troubleshooting plant/process problems.
Scheduling and coordinating work to tight deadlines
and within financial budgets. Ensuring that
equipment works to its specification and to
appropriate capacities. Assessing safety and
environmental issues. Liaising with
installation/project engineers and specialists.
Ensuring safe working conditions and compliance
with environment, health and safety.
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 RESPONSIBILITY WITH 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 & PPIC.
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. train new staff members in process
and procedures. Work with project team members to analyze their requirements.
15. Liasioning work .
. Project Undertaken
3. A - IN CAPSUGEL HEALTHCARE LLTD
1. Technology transfer – Value in Process(recuperation of Hard gelatin capsule shells) and system up
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(Sr. Process engineer).
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. PRODUCTIVITY IMPROVEMENT: Part of Team 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.
TRAININGS
1- EHS
2- Process flow- From URS to User end -Capsugel
3- GMP Aspects ( CALGS)
4- QA Aspect ( CALGS)
5- Leadership in Action
6- Dissolution in pharmaceuticals- NIPER
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 up to commercial production.
4- cost reduction and limited usage of overprinting material,strap rolls,polybags with better quality.
5- Got man of the match in Cricket tournament final match of 5 institutes and we won that Trophy
4. Declaration: I hereby to confirm that all Information given in my Resume are true and Authenticate through
my Knowledge.
THANKING YOU DATED 14/06/16
PLACE: Haridwar.Uttarankhand (AMIT SHARMA)
