CURRICULUM VITAE

[pic] KRISHAN KUMAR

DINDHORIA

PRESENT ADDRESS

HOUSE NO.:-5/15 SECTOR-5

U.I.T COLONY BHIWADI

RAJASTHAN 301019

Mobile:080********

Email: abgrgm@r.postjobfree.com

CAREER AIM

To be there where I can exaggerate my knowledge and explore my skills to

become a part of today's technology.

PROFILE SUMMERY

A Quality Assurance professional with experience more than 8+ years in the

good pharmaceuticals industries both in factory and corporate level. Proven

leadership skills involving managing, developing and motivating teams to

achieve their objectives. Dedicated to maintaining high quality standards.

Able to work on own initiative and as part of a team.

Endeavor

To become a distinguish professional in the area of Quality Assurance.

Personal Aptitude

Discipline, Sincerity & performance are the essence to my existence.

EDUCATIONAL QUALIFICATIONS

Exam Passed Passed Out Board/University division

M.Sc. 2004 Barkatullah University, Ist Div.

(Biotech.) Bhopal

B.Sc. (Medical) 2002 MD University, Rohtak IInd Div.

10th+2 1999 H.B.S.E Board llnd Div.

(Medical)

Matriculation 1995 H.B.S.E Board IInd Div.

CARRIER ACHIEVEMENTS

> About eight years plus work experience in Quality Assurance both in

factory and corporate level.

> Lead the QA team for Successful Certification for UKRAINE, W.H.O.

> Developed a proactive IPQA team to counter act the day-to-day problems.

> Solved major quality assurance problems, which temporarily halted in

production, with support from department heads.

CUURENT APPOINTMENT: 25th NOV. 2010 to till date.

Designation: ASSISTANT MANAGER Q. A.

Company: LARK LABORATORIES INDIA LIMITED BHIWADI (RAJASTHAN)

Company Profile: LARK LABORATORIES INDIA LIMITED which is situated in

BHIWADI (RAJASTHAN) is a WHO - GMP certified truly exports oriented

organization with annually turn over more than 100 crore.

AUDIT EXPOSURE

WHO -GMP

GMP- KENYA

EU -GMP

GMP- COMBODIA

GMP-NEPAL

Present job profile:

1) Preparation and review of all Departments Standard operating

procedures (SOP's) for cGMP compliance.

2) Implementation of cGMP practices in the facility.

3) Responsible for In-process of products.

4) Preparation and update the Site Master File.

5) Preparation of Annual Product Reports.

6) Investigation of root causes and implementation of corrective and

preventive actions.

7) Handling of Deviations, Non-conformances, Out of Specification, Change

Controls and CAPA Tracking.

8) Preparation of Training syllabus, Training needs, Training modules &

training calendars. Imparting training on shop floor.

9) Review Master BMR's and BPR's.

10) Supporting Validation activities. HVAC validation, cleaning

validation, Process validation and also preparation of all type of

qualification documents.

11) Assuring seniors in conducting Self-inspection/internal Audits at

plants.

12) Co-ordination with Validation team to perform validations.

13) Preparation of IQ, OQ, PQ of Equipments.

14) Attended few important trainings conducted by external party regarding

cGMP.

15) Coordinating with rest of departments for smooth functioning.

16) Knowledge of Temperature Mapping and done by External.

17) Training to Fresher's & New Joining.

Details of Experience

1) Experience as an Assistant Quality Assurance Chemist with Brawn

Laboratories Limited. N.I.T. Faridabad (An ISO 9001-2000 WHO, GMP

Certified) since 7th Sep. 2004 to 18th Oct. 2005.

Company Profile: - Brawn Laboratories Limited is a WHO GMP and 9001-

2000 certified company with annual turnover of 150 crore with a strong

performance in domestic and international market manufacturing wide

range of pharmaceutical product like Tablets, Capsules, Syrups, Cream,

Ointments and parental.

2) Experience as a Q.A. Executive with Synmedic Laboratories Sec-31 HSIDC

Faridabad. (An ISO 9001-2000 WHO Certified Pharmaceutical Company)

since 10th Nov. 2005 to 21st Sep.2008.

Company Profile: - Synmedic Laboratories is a WHO, GMP and ISO

Certified

Company with annual turnover of 100 crore with a strong performance in

the International Market and CIS countries. The company has the

approx. 10% domestic Market also and ready for enter the US and Europe

Market.

3) Experience as a Sr. Executive Q.A. with Gracure Pharmaceuticals Ltd.

Bhiwadi. (An ISO 9001-2000 WHO & also EU-GMP Certified company) since

25th Sept. 2008 to 03rd Sept. 2010.

Company Profile: - Gracure Pharmaceuticals Limited is an ISO, WHO, GMP

and EU-GMP Certified Company with annual turnover of 150 crore with a

strong performance in the International Market of Russia and CIS

countries. The company has the approx. 5% domestic Market.

AREAS OF EXPOSURE

> Knowledge of all Quality Assurance related activities and internal

audits.

> Qualification and Validation & all related documents.

> Knowledge of In-process work of all sections like Tablet, Capsule,

Dry syrup, Liquid, Cream, Ointment & Parental section.

> Flair knowledge of Regulatory work and well versed with CTD and

ACTD.

TRAINING UNDERGONE

. "ONLINE DOCUMENTATION" Conducted by Jimmy Karihalu

. CGMP & EU-GMP Training conducted by S.W. Kolhatkar.

. Qualification & Validation by Gery Demarteau.

. Market & Product recall by Gery Demarteau.

. Risk Assessment by Gery Gemarteau.

. "HACCP" Training conducted by S.W. Kolhatkar

. Many more conducted in house.

INTEREST

My interest is to continuously work on my general awareness. I do this by

watching informative programs and reading books.

VALUES

Commitment, Dedication, Discipline, Self confident, Hard working, punctual,

positive attitude and very honest towards my work.

PERSONAL PROFILE

Name : Krishan Kumar Dindhoria.

Father's name : Sh.H.S. Dindhoria.

Mother's name : Smt. Geeta Devi.

Date of birth : 3rd November 1978.

Nationality : Indian.

Marital Status : Married.

Languages Known : English, Hindi, Punjabi & Haryanvi.

Permanent address : House No. 1639 Sec-23/A

Housing Board Colony

N.I.T. Faridabad

HARYANA

PIN-121005

Salary Drawn : Rs. 5.0 Lac per annum.

Place

(Krishan Kumar Dindhoria)

Date

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