To,
The HR manager
Zuventus Healthcare Ltd
Bangalore
Respected Sir,
With the reference to above, I would be thankful if you offer me good Position in your esteemed
company.
I take this opportunity to introduce myself - Krishna Kumar Mahto as graduate in B. Pharmacy from Biju
Pattnaik University of Technology, Rourkela in year 2012, with a vision to excel with an experience of 9
years 8 Months. I have good exposure in Production activities. I have proved the best during my
services to the organization.
At present, I am working for Zuventus HealthCare Limited. Bangalore as an executive in Production
Department from JUN-2017. I understand that working for your organization requires a candidate who is team oriented and can deal with
people in various departments. I am confident that I process these skills, which will help me
to perform the job effectively.
My goal is to transit my enthusiasm, Productivity & experience into a position, where I continue to provide the
quality output critical to organization growth. I make certain that, my presence in your team will prove to be
beneficial to your organization. As such, I would welcome an opportunity to
speak with you to evaluate your needs & share my ideas. Looking for an opportunity to utilize my skills and abilities towards
the field of pharmaceutical formulation that offers me personal &
professional growth while being resourceful, innovative, and
flexible. I would like to work around high knowledge environment,
gain expertise, and thus make myself an asset of the organization.
Overview
4
years of professional experience
Work History
Zuventus Healthcare Limited
EXECUTIVE -Production
06.2017 - 01.2017
Encube Ethical pvt
Ponda, Goa
OFFICER
01.2016 - 01.2017
Pharmaceuticals, Zuventus Healthcare ltd
Bangalore
Production Chemist
01.2013 - 01.2016
Job overview
To ensure manufacturing, Filling and packing activity are carried out at the plant are as per defined
SOP/work instructions and in compliance to the cGMP
To ensure all safety procedures are followed as per the legislation and RB EHS Guidelines
To ensure effective cleanliness and maintenance program for facility and equipment
To achieve production as per the production targets
Preparation and implementation of approved Standard Operating Procedure (SOP), document of production
and batch documents
To raise change control in Quality one system and implement necessary changes as defined in the change
control
To coordinate and carryout for validation activities as per validation master plan
To issue batch requisition and co-ordinate with store personnel for receipt and verification of the issued
material
Key person in handling Unionised organization
Wellverse in getting penetraing company goals and targets to Union office bearers with smooth
understanding and implementation
Achievements:
Planning of packing lines as per monthly target and achieving the target as per Market requirement
Reduce the manpower by modifying the packing lines
Increased the production capacity upto 40% more by getting involved as key member in process
improvement projects
Successfully started New manufacturing suit (brown field project) – installation of New
Manufacturing and Storage vessels of 10KL X 3 vessels
Implemented CIP / SIP in new manufacturing suit
New validation batch execute succufully.
Group Pharmaceutical ltd
Supervisor
Job overview
As a, In-Charge Production I was responsible for…
Preparation and review of department BMRs, SOPs, Logbooks and GMP documents
To co-ordinate with QA/Engineering department to carry out the qualifications (IQ/OQ/PQ) activities to
the new equipment’s
Training given to all sub-ordinates about the manufacturing activities which should be done by complying
GMP aspects
To perform the filling activities and documentation of filling the cream, ointment, lotion and toothpaste
Arrange all the requirements in advance to do the day-to-day activities successfully without any time delay
and giving the pre-intimation to other departments about the daily production
activities
Raising the purchase request of all required operational supply items and to maintain the inventory
control of all these items
Whenever any unusual observations observed by QA or production, it will be addressed through proper
Quality management system like initiating the Deviation, QA Notifications, or temporary change control
To co-ordinate with QA-Validation to carry out the cleaning validation and process validation of Semisolid
filling facility
Load cell usage and verification of load cell
Achievements:
Product manufacturing vessel - 10000 lts (Pharmatech) - inlcudes HMI based operation system which
included CIP / SIP
pH meter (Pico +)
Inline homogenizer(modern engineering)
Colloidal Milling Machine
(Image)
Ink jet printer (Control Print)
Cross- verifying the dispensed raw materials and transfer to the compounding area through material air
lock
Arranging the basic requirements to manufacture the products
Maintain the Equipment/Area usage and cleaning logbooks according to the day-to-day activity
Operating the manufacturing equipment and carry out the manufacturing process as per the batch
manufacturing record instruction and record the observation and time details in the
records online
Achievements:
Increased the packing quantity of Bottles from 35000 to 1Lac bottle production per day
Qualification of new equiments
Implemented online shipper weighing mechanism
Undergone for training on Hygenic design and microbial contol codcuted by Johnson and Johnson
Encube ethical pvt.ltd
Handling the manufacturing and filling equipments Semisilod ,Ointment,Cream,Lotion
Monitoring the filling and packing activities and filling the batch packing records online
Maintaining the area and machine logbook and update the activity online
Calibration of preparation & storage vessels
Allocation of manpower according to production plan and work priority
Training Technicians on equipment operation, Safety and production process
Major Milestone
Got success in ISO, GSK, Pfizer & J&J Audits without any major observation
Improved the investigation skill of cross functional team at site and strengthen the deviation
Management system
Lead role from production for Process validation, FMECA and other QMS documents
Key person in improving the Production output of Sensodine by reducing
Process time
Introduced the robust guidelines during COVID time which ensured the zero Production
stoppage as well good health of the work force
Lead role in Project CAN DO (Cost savings project) - Reduction of Pages of batch Records which
leads to cost saving, process improvement
Improved the Equipment qualification and validation documents and as per the regulatory
requirements and guidelines
Overall Equipment Efficency has been standarzied and OEE increased from 60% to 68% by altering the
machines
Providing the Basic GMP training to shopfloor personnel
Attended the training on Hygenic Design requirment provided in Zuventus healthcare ltd
Successfully qualified new suppliers for Raw Materials and Packaging Materials by taking trials and PV
Batches
Successfully participated in Uganda & Kenya audit in Zuventus healthcare ltd in 2022
Successfully participated in Customer audits - GSK, Pfizer & J&J in Encube ethical pvt