1. #Flat No. S-3 Prabhukripa Homes, Peermuchalla
Dist: Mohali SAS Nagar,pincode 140603.
e-mail :- gaurav_rajvanshi2004@yahoo.co.in
gaurav.rajvanshi2010@gmail.com
Mobile No:-09780128673
09041748352
Gaurav Rajvanshi
Date of birth April 08, 1979
Marital status Married
Nationality Indian
Experience 12.0 years
Objective: Looking forward to associate myself with an organization, where there is an opportunity to continue and
upgrade my knowledge and professional growth for self and organization served.
Highlight of professional career:
1. Excellent exposure to product manufacturing, having independently headed large sections of granulation,
compression, capsules, coating and Pellet coating .
2. Handled all types of dosage forms manufacturing (Tablet, Capsule, liquid, semisolid and Dry Syrup).
3. Key role-played in regulated market approvals of
WHO-GMP, USFDA, MHRA, ANVISA, TGA, EMEA, ISO 9001: 2000, OHAS, IDMA, UNICEF, YAMAN
REGULATORY AGENCY,UKRANE,KENYA,GCC.
4. Significant contribution in the field of production operation and training of plant personal during the career
span.
5. Excellent exposure to Quality assurance, regulatory & formulation
6. Key role-played as a coordinating team member of ISO 9001:2000 & get appreciation letter from the
higher management in Ind Swift ltd. Parwanoo.
7. I have got certificate for successfully completion of training for ISO 9001:2000 in Ind Swift ltd. Parwanoo.
Personal Skills: Comprehensive Problem Solving abilities, excellent verbal and written communication skills,
Willingness to learn and very good team facilitator.
Education : Passed Matriculation from K.K. INTEER COLLEGE MEERUT, in 1995 from U.P. BOARD
Passed +2 Sc from K.K. INTEER COLLEGE MEERUT, in 1997 from U.P. BOARD
Passed B.PHARMACY from H.N.B.G.UNIVERSITY SRINAGER GARHWAL , in 2003 with 64% marks.
Computer skill : Knowledge of Computer Applications.
Platforms Known: WIN 2007, WIN XP and MS-DOS.
Software Known: MS-Office with Internet, ERP, CITRIX, SAP

2. Professional experience : -
1. (May 2010 to till date)
Working as Executive Production in Torrent pharmaceutical ltd. Baddi Himachal Pradesh.
Job Profile :
 Review and submission of BMR after completion of manufacturing process and carryout the investigation if
any discrepancy found during the reviewing the BMR.
 Handling of Deviation and change control and prepare the investigation report for the same.
 Active participation for timely installation, commissioning and qualification of all the equipments and
processes validation in the Formulation facility.
 Leading team member from production to give technical assistance to FR&D products and Process
validation.
 Responsible for daily production targets, generation of daily production reports, capacity utilization and yield
statements, preparation of month wise yearly budget.
 Co-Ordination With Qc, Qa, store & Maintenance for production of pure and effective medicine with safety
measures.
 Execution of Daily, weekly, monthly production schedule.
 Execution of day to day activities related to production documentation as per cGMP and SOP’s.
 Improvement of Manufacturing Process by Formulation development On sop floor.
 Increase in productivity and yield by process Development.
 Preparation and Review of Standard Operating Procedures (SOP), Work Instructions (WI), and
manufacturing batch records for Formulation manufacturing.
 Execution of Exhibit and Validation batches and effective co-ordination with the formulation research team
for the technology transfer of Products.
 Ensuring on-line completion and review of all documents such as Manufacturing batch records logbooks, etc.
 Training of operating personnel on the operational and cGMP aspects of the equipments / processes and
systems to ensure timely start of Production operations
 Execution of the production plan and meeting all the delivery schedules for the products as committed in the
Plan.
 Maintaining and up keeping the area as per the cGMP and Regulatory requirements and putting continuous
efforts for improvement in quality and Productivity.
 Handling manpower (work allocation), resolving issues on the shop floor, team building and team player.
 I have experience in handling of granulation, compression, coating, activities. and, able to handle Sejong,
cad mach compression machines
 Skillful allotment of production duties amongst the production chemist and worker for daily shop floor
activities
 To identify and provide training to new staff and operator.
 Export order planning from dispensing to semi finished goods..
 Thorough knowledge of operation, calibration, trouble shooting, and preventive maintenance of production
Equipment.
 Preparation, filling, Review and compliance of BMR, BPR, MFC, Process validation protocol , Process
optimization report, Process validation report.
 Implementation and Improvisation of method as well as procedures for proper utilization of man power,
Equipments and materials to achieve productivity.
 Inventory control: of sieves, screens, finger bags and vent filters.
 Preparation of monthly work in process inventory. and Yield reconciliation of in process materials.
2. (DEC 2009 TO May 2010)
Working as Executive Production in MYLAN(MATRIX) LABORATORIES LTD. NASIK (M.H.)
Production activity
 As a Executive production planning and scheduling of production activities.
 Involved in day to day activities like compression, capsulation
 Leading team member from production to give technical assistance to FR&D products and Process
validation..
 Responsible for daily production targets, generation of daily production reports, capacity utilization and yield
statements..
 Co-Ordination With Qc, Qa, store & Maintenance for production of pure and effective medicine with safety
measures.

3.  Execution of Daily, weekly, monthly production schedule.
 Execution of day to day activities related to production documentation as pre cGMP and SOP’s.
 Improvement of Manufacturing Process by Formulation development On sop floor.
 Increase in productivity and yield by process Development.
3.0 (MAY 2007 TO DEC 2009)
Working as officer Production in ALKEM LAB.LTD.BADDI
Production activity
 As an officer production responsible for execution and scheduling of production activities.
 Involved in day to day activities like dispensing, granulation, compression, coating and capsulation .
 Responsible for daily production targets, generation of daily production reports, capacity utilization and yield
statements..
 Co-Ordination With Qc, Qa, store & Maintenance for production of pure and effective medicine with safety
measures.
 Execution of Daily, weekly, monthly production schedule.
 Supervision of day to day activities related to production, dispensing, batch preparation, and documentation
as pre cGMP.
 Improvement of Manufacturing Process by Formulation development On sop floor.
 Increase in productivity and yield by process Development.
 To raise BMR requisitions for taking the Batches from Q.A. dep’t.
 To prepare the document of equipment qualification and calibration data.
 To prepare the process flow diagram with validation parameter.
 Preparation of validation sampling plan.
 To set up the critical parameter and acceptance criteria.
 Validation of process for the formulation of tablet, capsule & dry syrup.
 Validate the suitability of materials and the performance and reliability of equipment / system.
 To trouble shoot any technical problems or equipment problems
4.0. (SEPTEMBER 2004 - MAY 2007 )
Worked as Executive Production in production Department of Ind-Swift Ltd,
Unit – I,2 & 3 Parwanoo and Baddi Himachal Pradesh
 To execute the production manufacturing schedule and co-ordination with the Q.A. Deptt.
 To have effective control on manpower on daily basis.
 To ensure on line documentation of production activity.
 To guide the production operators and helper in case of any problems or issues.
 To ensure strict adherence to SOP’s during all stages of production.
 To correct the people by training who are violating GMP or who are working ineffectively.
 To handle granulation, compression, coating & capsule dept. Some time in packing dept. also
 To maintain cleanliness of the machine and working area in presenting manner.
5. (may-2004 – SEPT. 2004)
Worked as Junior Production chemist in production Department of NEW LIFE PHARMACEUTICAL PVT. LTD. Okhla
new Delhi, it is a WHO GMP approved organization having facility for Tablet, Capsule,& liquid
 Handling manpower, prepare profile of manpower in shift wise.
 Meeting the monthly production target and yield.
 Meeting quality standard as per customer’s specification. Handling various production matters related to
machines, Compression machine, etc.
 Handling all the Activities regarding Production of Tablet and Capsules Departments.
 Process operation as per SOP and process guidelines Interaction with different service departments to run
production smoothly.
 Preparation & Review of SOP.
Personal Details : FATHERS NAME : Dr. Narendra Kumar Rajvanshi
PERMANENT ADDRESS : 322,Brahumpuri Lane opp.power house, Meerut
Dist: MEERUT (U.P.)
Notice period : Three month
Present salary : 8.0 lac / Annam

4. Expected Salary: Negotiable
DECLARATION : I do hereby declare that the data submitted above are true to the best of my knowledge and
belief.
Place: GAURAV RAJVANSHI
Date: