CURRICULUM VITAE

VIDHYASAGAR SHARMA
Mob.: 07733843080, 09694718040
Email: vidhyasagar25@gmail.com

Career Objective
To achieve personal and professional growth in whichever field of work to accept challenging job
opportunity which could reveal my inner talent & help me to emerge as a competent & satisfy my urge
tolerant more & more.

Working Experience (9 Year 7 month)

 Presently Working as a Sr. Executive at Ahlcon Parenterals (India) Ltd. Bhiwadi Raj.(A
B/ Braun melsungen Group co.) Since Apr. 2018 to till date & As a Executive from Jan.2016
to Mar.2018
M/s Ahlcon Parenterals (India) Limited a B.Braun Group Co. Is located in Bhiwadi Rajasthan and
WHO & EU GMP approved plant. B.Braun Group Co. is Germany based MNCs and 100% share
holder of Ahlcon Parenterals India Limited; it consists of state of art facility meeting all the
international standards. It is one of the leading manufacturers of pharmaceutical products of our
export and domestic market & all multinational companies like Sun Pharma, Cipla, Zydus Cadila,
Dr.Reddy etc.
 Previously Worked as a Sr officer at Albert David Ltd. Ghaziabad U.P. (A Unit of Kothari
group) since month Apr-2015 to Jan 2016 .
Albert David Limited is a Kothari Group of company and having a business of Pharma, APIs and
Medical Devices, tea, textiles and engineering. Albert David Ltd., Ghaziabad is the manufacturer
of Large Volume Parenterals (LVP) in Plastic and Glass, Small Volume Parenterals (SVP) in
plastic vials and Capsules and having a turn over of approx INR 350 crores and group turn over
approx 4500 crores. Albert David Limited, Ghaziabad has been approved from WHO, Uganda,
Ethiopia, Nigeria, Belgium, Peru etc. regulatory bodies and also having a certification of ISO
9001:2008 and ISO 14001: 2004.
 Previously Worked as a Jr Executive at Ahlcon Parenterals (India) Ltd. Bhiwadi Raj.(a B
Braun melsungen Group co.) since month Apr-2012 to March 2015. & As a Officer since
Month Jan.2010 to Apr.2012
 Previously worked as a QA-Chemist at Lark labs. Pvt. ltd Bhiwadi Raj. (Formulation Unit of
Tablet & capsule) since month Sep.2009 to Jan. 2010.
Key Responsibilities:

Quality System implementation and their Compliance, Training, Internal and External audit,
Validation, Qualification, Calibration, IPQA activity, Annual Product quality review , Change Control,
Deviation, Investigation , CAPA & Stability study
VALIDATION & QUALIFICATION ACTIVITIES
 Responsible for Preparation & Maintain Validation Master Plan to ensure compliance with regulatory
requirements and current industry practices.
 Responsible for planning and cordination with external agency for validation and calibration activities
as per schedule and Preparation of Validation and calibration planner.
 Responsible for Qualification ,Validation, Revalidation and Calibration activity for Equipment &
Instruments , Its Documents preparation , Execution & Review.
 Responsible for equipment qualification and periodic re-qualification of Direct Impact Systems

e.g., Mixing & Holding vessel, BP machine, Autoclave, terminal sterilizer, other production
equipment , Store equipment , Packing equipment , QC & Micro instruments.

 Responsible for utility qualification and periodic qualification e.g., Water system , Compressed air ,
Pure steam & Nitrogen air qualification , Its Documents preparation , Execution & Review.

 To responsible for Aseptic process simulation (media fill for SVP line) its Execution & Preparation
of Report.

 Responsible for HVAC System & A- Grade Equipment qualification periodic qualification.Its
Documents preparation , Execution & Review of the document .
 Responsible for process validation & Cleaning validation ,Its Documents preparation , Execution &
Review of the document .
 Responsible for other Re-validation study e.g. Equipment Hold time study, Visual checker
qualification study, Steam in place validation study , Temperature mapping study .
 Responsible for cordination with external person for PLC validation and review the document .

DOCUMENTATION & QMS ACTIVIES

 Responsible for monitoring adherence to various cGMP activities at site.
 Ensure to maintain Quality Management System and their compliances from dispensing to dispatch of
finished products to produce quality products.
  Responsible for the preparation Annual Product Quality Review (APQR) according to the schedule
and batch manufacturing record.
 Responsible for BMR review and release the batch for sale/ supply.
 Responsible for log, investigation and review of Change Control and its management as per standard
procedure.
 Responsible for log, investigation and review of Deviation and its management as per standard
procedure.
 Responsible for log, review and monitor of CAPA and their follow-ups.
 Responsible for conducting self-inspection as per inspection schedule. Review and compilation of
Self Inspection reports.
 Responsible for Audit compliance and their follow-ups and response.
 Responsible for preparation and review SOP.

cGMP COMPLIANCE & IPQA ACTIVITY

 Identification of NC’s and follow up to respective officer/ H.O.D. for their compliance on daily basis,
from production.
 To ensure environmental and microbial monitoring, batch manufacturing activity control in Clean
room.

 Ensure cGMP compliance in Production area. & clean room .

 To ensure sampling activity during batch manufacturing, process validation, cleaning validation.
 To Responsible for monitoring and ensuring on line review of batch manufacturing document, batch
packing document and log books.
 To Ensure control sample management.
 Handling of equipments such as: Anemometer, Non viable particle counter, Viable air sampler, lux
meter, Palltronic flowstar intergrity M/C, Compressed air Gastec assembly, Temperature data logger
etc

Professional
Professional Qualification
Qualification

B. Pharma from B.N.P.G. College of pharmacy Udaipur with first class, Affiliated by Rajasthan
University of health science. Approved by PCI & AICTE.
Audit Exposure
WHO CDSCO , Nigeria, NAFDAC, Ethiopia, EU GMP & Customer Audit : Cipla Ltd., Dr, Reddy’s,
Sun pharma, Glenmark, Cadila, Exphar, IPCA, Lupin, etc.

Computer skills

Ms-office and internet working.

Skills Acquired

 Ability to work in a team as a leader or as a responsible.

 Confident and Positive attitude.
 Hard-working & Honest.

Personal profile

Date of Birth : 25 Jan 1987

Marital Status : Married
Father’s Name : Shri moolchand Sharma
Languages : English, Hindi
Permanent Address : Pahari Distt. –Bharatpur (321204) Raj.

Declaration

I hereby declare that all the information furnished in the present resume is true to the best of my belief
and I promise that if given a chance, I would prove myself to be an asset to your organization.

Vidhya Sagar