CURRICULUM –VITAE

VAIBHAV K. TIWARI E-Mail :- vaibhav.tiwari40@gmail.com

6, Bada Bazaar Ganesh Mandir Rau
Mob :- 9926344986, 9691901121

OBJECTIVE :-

 To working in challenging environment which conductive or development & learning & in

Process creates a symbiotic relationship with the organization.

PERSONAL DETAILS:-

Father’s Name : Shri Rajendra Kumar Tiwari

Date of Birth : 01st – Dec – 1984

Language Known : Hindi & English

Nationality : Indian

Martial Status : Unmarried

PRESENT JOB DETAILS:-

 Working as a Management staff Section Head (Sr. Production Executive) in Cipla LTD. at
Indore SEZ (Pithampur).

CARRIER SUMMARY:-

 Been in operation for the past four years in various roles as a production supervisor
production Officer & now as a Sr. production executive.

SOMETHING ABOUT ORGANIZATION:-

 Cipla is an ISO 9001-2000 WHO-USFDA certified organization it is heaving wide variety of

Pharmaceuticals products human as well as veterinary.

ACHIVEMENT:-

 Performed FAT (Factory Acceptence Test) of flow wrapping machine/pouch packing

machine in Beijing china.
ACADEMIC PROFILE:-

 Graduate in science Biology/chemistry from Holkar Science College.

 H.S.C. from M.P. Board Bhopal
 S.S.C. from Keshar Vidya Niketan (M.P. Board Bhopal)

OTHER QUALIFICATION:-

 1 year computer diploma exposer to work with MS Excel, MS word, Windows 2007,MS
Office , Fox Pro & having grade A by Academic Council.

AUDIT FACED:-

 Tanzania drug & food association (TDFA) – Tanzania.

 National drug authority (NDA) – Uganda
 Drug authority & control agency (DACA) – Ethiopia
 Food & drug Board (FBD) – Ghana
 Ministry of Health (MOH) – Yemen
 Medicine and healthcare product agency -MHRA

JOB RESPOSIBILTY:-

 Responsible for all filling & packing activity related to FFS department.
 Improvement, continuous review and up gradation of existing production SOPs and work
system and to ensure their strict implementation.
 To fill, evaluate and sign all document before they are made available to quality assurance
department.
 To restrict deviations / noncompliance’s and working for zero market complaints.
 Preventive and corrective actions for observed non-conformance.
 To coordinate with planning, R&D, prc department for technology transfer.
 To ensure proper planning and execution of the batches in accordance with the plan.
 To conduct risk analysis of product, system, Equipment, item, process in order to obtained
the required quality. FMEA (Failure mode effect and critical analysis).
 Perform validation of packing & filling equipment as per validation protocol, and
documentation as per validation report.
 Prepare the DQ/URS/IQ/OQ/PQ of packing and filling line equipment.
 Raising the capital expenditure requisition / indent to fulfill new requirement and maintain
inventory.
 Co-ordinate with the stores,QA,QC to exceed the plan and activities,
 Perform calibration/verification.
 Creation of formulation code, manufacturing code, batch number, BMR, EMCM and EMRM
in production system.
 To plan manpower requirement required for filling and packing line activities with respect to
planning.
  Maintain achieved productivity level & further improvement Constantly to meet the
market requirements.
 Training sub-ordinate and workers.
 Perform any other consignment allocated by Unit Head and Department Head.

SPECIAL ASSIGNMENT-
 To optimize the set facilities to maximum productivity in terms of yields and output.
 On the job & classroom training to the fresher technicians on different aspects.
 Member of Task force team.
 Finalization of Documentation such as subsequent development of Batch
Documents.

PROJECT UNDERTAKEN:-

 Participation in installation of FFS machines(weiler) pack leaders(Taiwan ) respules , unims

& vial labeling machine, check weigher (Nikka densok Japan), pouch packing
machine(omori Japan) terminal sterilizer (fedegari), Deflasher machine( skan USA) Pinhole
Inspector (Nikka Japan) Sleeving and shrink tunnel machine, CAM Cartonator (Italy).
 Prepare document, design qualification, installation qualification, operational qualification, &
performance qualification.

ATTEND TRAINING SESSION:-

 Validation of sterilization processes by Mr. Nigel Halls (Brighton. UK) \

 Cross contamination & Contamination control
 Documentation in pharmaceuticals in manufacturing, cGMP, Personal Hygiene & many
more.

TECHNICAL EXPERIENCE:-

 Well known knowledge of FBS machine, FFS machine( Weiler USA), Pack leaders
Respules, Unims & vial labeling machine, check weigher(Nikka densok Japan), pouch
packing machine, terminal sterilizer(Germany), pouch labeling machine(Taiwan), Sleeving
& shrink tunnel machine(Pack leader Taiwan), CAM Cartonator (Italy).

EXTRA CURRICULAR ACTIVITIES:-

 Participated in cultural activities in school & college

 Participated in wrestling in under 65 Kg’s Weight & secured Ist Position.
INTEREST & HOBBIES:-

 Cricket, Chess, Wrestling, Listing Music.

PROFESSIONAL:-

 Familiar with the basic requirement as per USFDA GMP norms for production.

REFERENCE:-

 Shri Jitendra Vyas former HR head M/s Ipca Laborites Ratlam (M.P.) and presently working
with Essar Group as HR head Hajire (Surat).
 Shri Shreerang Chopde former general Manager M/s Anglo French, Pithampur (M.P.).
 Shri Ashish Shrivas Department head Cipla Limited Pithampur.

DECLARATION:-

I here by declare that the above given information is true & best of my knowledge & belief.

I hope you consider me & give the opportunity to serve your organization I will submit you
Necessary certificate at the time of interview.

Date:………… (VAIBHAV K. TIWARI)