www.brawnlabs.com Brawn Laboratories Ltd Delhi : Regulatory Affairs Executive

[mskavi]

Brawn Laboratories Ltd. Delhi : Regulatory Affairs Executive
brawnlabs.com

Designation: Regulatory Affairs Executive
Experience: 1 - 4 Years
Location: Delhi

Job Description:
Preparation, review, and evaluation of documents for submission to regulatory authorities in Semi-regulated & Un-regulated countries.
Review of BPR, Stability data,COA’s.
Involved in development of packaging components.
Timely response to Queries.

Desired Candidate Profile:
Candidate should be thoroughly familiar with registration requirements for regulated and semi-regulated markets. Basic knowledge of Pharmacopoiea.
Experience in QC/QA is preferred.
Aware of country wise registration guidelines and filling of dossier.

Company Profile:
Brawn Laboratories Ltd. is a successful manufacturer and exporter of a wide range of quality innovative products for health care industry Certified by ISO 9001:2000,WHO cGMP,vouches to consistently progress ahead for making quality health care products

Website: www.brawnlabs.com

Keywords: Regulatory Affairs Executive

[anupama upadhyay]

dear sir
myself anupama upadhyay post graduate in biotechnology and i would like to join your organisation as a dra please update me with your requirments. my mail id is upadhyayanupama_anu AT rediffmail.com/anu_upadhyay1606 AT yahoo.com .
cnt no;

[vikassingh_2511]

i would like to join as a process engineer in pharma industries.

[neha pande]

Hi,
I am presently working as regulatory affair executive . I am keenly interested to join your esteemed organisation. If any vacanies related to my profile please update me. My mail id : nehapantin@gmail.com.

Thanking You ,
Neha Pande

[Guest]

Respected sir/ mam,
myself soni saxena from Rajasthan. presently i m working as a medical representative in Bestochem Formulations. i have a question that, i completed my MBA from CSMM[Chemical Sales and Marketing Management]from Jiwaji university[Gwalior], but in that course i had all the same subjects like as B. Pharme and M. pharma., then can i try for manufacturing or production or H.R. or product management in pharma sector.
pls reply me as soon as possible.
thanx
soni

[Guest]

APPLICATION LETTER
I am D.pharm and B.pharm passed out candidate. I had completed my diploma in pharmacy from M.N. College of pharmacy, (Khambhat) affiliated to Gujarat University at 2008. And my B.pharm is completed from C.U.Shah College of pharmacy and research, (wadhwan) affiliated to Saurastra University, from 2011.
I had a first class aggregate in B.pharm and desperately likely to work in your company at any suitable required post. I had attached my resume which gives the detailed information. Therefore, please kindly respond to this letter.

CURRICULUM VITAE

Email- nagrale.abhishek AT gmail.com
nagrale_abhishek AT yahoo.in
NAGRALE ABHISHEK KISHORBHAI
CAREER OBJECTIVE
- To start career with an organization that provides excellent job opportunity and which enables me to apply my skills to achieve best organizational objectives.
EDUCATIONAL DETAILS
D.PHARM AND B.PHARM (REGISTERED PHARMACIST)
EXAMINATION MON/YEAR OF PASSING BOARD/
UNIVERSITY MARKS OBTAINED OUT OF PER.
S.S.C. MARCH 2004 G.S.H.S.E.B 358 500 74.00
H.S.C. MARCH 2006 G.S.H.S.E.B 394 650 60.61
D.PHARM- I APRIL 2007 GUJARAT UNI. 603 1100 54.81
D.PHARM- II APRIL 2008 GUJARAT UNI. 500 1000 50.00
1st B.PHARM MAY 2009 SAURASHTRA UNI. 467 700 66.71
2nd B.PHARM APRIL 2009 SAURASHTRA UNI. 759 1300 58.38
3rd B.PHARM APRIL 2010 SAURASHTRA UNI. 777 1200 64.75
4th B.PHARM APRIL 2011 SAURASHTRA UNI. 913 1400 65.21
I had completed my D.PHARM from M.N.College of Pharmacy which is affiliated to Gujarat University while B.pharm from C.U.Shah College of pharmacy which is affiliated to Saurastra University & school from Axay higher secondary school affiliated to G.S.H.S.E.B. board.
Aggregate of the D.Pharm :- ) 52.40%
Aggregate of the B.Pharm :-) 63.47 %
COMPUTER AWARENES
- Certificate in M.S. Office
- Window 98, XP,
TECHNICAL COURSES KNOWN
- Inter-net,
TRAINING PROFILE
- 500 hours training as HOSPITAL PHARMACISTS at Civil Hospital, Ahmedabad.
ACHIEVEMENTS
- Workshop on use of blood at B.J.Medical College, Ahmedabad.
- Delegate as poster presentation on ARTIFICIAL BLOOD (pharma Gujfest 09) at Ganpat University, Kherva, Gujarat.
- Drawing competition on ‘DEFENCE’ 2002
PROFESSIONAL PROFILE
- I am REGISTERED PHARMACIST from 2008
- Highly organized and dedicated, with a positive attitude.
- Ready to accept challenge from surrounding to achieve the best.
- Believe in perfection in everything.
- Gives the best of myself.
- Have excellent interpersonal communication skills.
- Eager to learn regarding new technologies.
- Doesn’t get afraid of losing.
HOBBIES
- Playing chess, swimming, internet surfing & other outdoor games.
- Going daily gym.
- Listening songs, & play loud rocking music.
- Reading novels, books & different articles.
- Traveling.
- Like to use technology like GPS and Laptops.
- Eating new things from different culture.

[Guest]

Recently shifted to gurgaon looking for job in QA/QC or RA as i have experience in both these areas.mail id myspace2405@gmail.com

[Guest]

This is Premlata Rani and my updated CV is paste below this . Presently i am working with Health Biotech Limited atChandigarh. I have 2 year experience in pharma sector and one year inRA.
CURRICULUM VITAE
Premlata Rani
E Mail Add : latasingh127 AT gmail.com
CAREER OBJECTIVE
To achieve the highest position in the field of “Pharmacy” by applying my diversified knowledge with determination, dedication and hard work to develop innovative solutions to the Pharma Market.
PROFESSIONAL QUALIFICATION
B.Pharma from Lloyd Institute of Management & Technology (G.Noida) approved by Uttar Pradesh Technical University & PCI.
B. PHARM.
FOURTH YEAR 70%
THIRD YEAR 70%
SECOND YEAR 70%
FIRST YEAR 70%
EDUCATIONAL QUALIFICATION
- 10th +2 from U.P. BOARD in 2004 with 61.7%
- 10th from U.P. BOARD in 2002 with 54.6%
CURRENT APPOINTMENT : July 2011 to till date as Regulatory Executive with Health Biotech Limited Chandigarh.
COMPANY PROFILE :
WHO-GMP Certified Company & Adhering to UK-MHRA system .
PAST EXPERIENCE :
- ONE Year with Ahlcon Parenteral (India) Limited Bhiwadi (RAJ.) as RA EXECUTIVE
COMPANY PROFILE :
Ahlcon Parenterals (India) Ltd. has achieved the Quality Certification WHO – GMP International and ISO 9001 :2008.
Manufacturing Intravenous Fluids & Eye/Ear Drops by highly sophisticated Manufacturing process, From – Fill-Seal Tech.
- ONE Year with Gracure Pharmaceuticals Limited Bhiwadi (RAJ.) as RA EXECUTIVE.
COMPANY PROFILE :
Gracure Pharmaceuticals Limited Bhiwadi (RAJ.) It has near about 200 crore turnover annually and have well market in Europe and Russian countries. The Gracure Pharmaceuticals Limited is now an EU-GMP certified company having strong market Globally.
SUMMER TRAINING
Company : Aurochem (I) Pvt. Ltd
Add : B-74, Sector-2, Noida, 201301, India
Duration : 07-06-2008 to 07-07-2008
Worked in Production, QC and QA Department.
Friability Testing, Dissolution Testing, Weight Variation.
Tablet Manufacturing.
RESPONSIBILITIES HANDELED as a RA Executive
- Preparation of Dossiers as per ACTD and CTD guidelines mainly for Vietnam,Singapore, Indonesia,
Tanzania , Kenya, , Trinidad , Tajikistan ,Taiwan ,Sudan ,Nigeria, Thialand ,Ukraine, Uzbekistan,
Greece, Turkmenistan, Philippines, Mission and Venezuela etc.
- Interact with various departments/ teams to collect documents required for regulatory compilation
on time as per regulatory norms.
- Preparation and review of query (dossier) response.
- Maintaining Regulatory documents as per the procedure.
STRENGTHS
- Honesty
- Team work
- Positive thinking
- Keen Learner with ability to learn and imbibe new knowledge with ease
- Hard Worker
- Sincere

SKILLS
Computer Basics :
- Ms Office-2003-2010
Date :
Place : (PremLata Rani)

[Guest]

CURRICULAM VITAE
Mr. AMAR NATH BARIK
E-mail : amarnathbarik AT gmail.com

CAREER OBJECTIVE :
Looking forward to an appropriate opportunity of my academic and technical domain in a Pharmaceutical Industry where I can utilize my skills effectively leading to my employer and my success.
INDUSTRIAL EXPERIENCE :

Project experience at GLENMARK GENERICS LTD., FORMULATION DEVELOPMENT DEPARTMENT (NDDS Group) Navi Mumbai
TECHNICAL ACHIEVEMENT :
- Qualified GATE (pharmaceutical sciences) in the year 2009 securing 94.34 percentile (AIR-1351, Score-439) conducted by Indian Institute of Technology ROORKEE
- Qualified the WIPO Worldwide Academy's Distance Learning course “General Course on Intellectual Property DL-101”
- Qualified Distance course of PHARMA REGULATORY AFFAIRS at Bioinformatics Institute of India, New Delhi
TECHNICAL SKILLS :
- Handled equipments used in Solid Orals such as Rapid mixer Granulator, Tablet Compression machine, Ganscoater, Multi mill, Fluidized Bed Dryer, V Cone Blender, Disintegration Apparatus
- Experienced on Solid Orals and Oral Liquids
- Experienced on Hormonal Product Developments
- Well versed with Technical Reports Preparations
COMPUTER SKILLS :
- Operating System : MS Windows, MS Words, MS Excels, MS power points, MS DOS
- Regulatory Literature Search
- Well versed with FDA web page

EDUCATIONAL QUALIFICATION :
Examination Passed Board / University Name of School/ College Year of Passing Marks
M. Pharm (Pharmaceutical Technology) Biju Patnaik University of Technology, Odisha Royal college of Pharmacy and Health Sciences, Berhampur, Odisha Pursuing
CGPA : 8.52 (77.7%) 1st Year
B. Pharm Biju Patnaik University of Technology, Odisha Roland Institute of Pharmaceutical Sciences, Berhampur, Odisha 2009 CGPA : 8.34 (76.1%)
12th CHSE, Odisha J.K.B.K. Govt.college, Cuttack, Odisha 2000 65.66%
10th HSE, Odisha Kalinga Vidyapith, Choudwar,Odisha 1998 72.93%
DISSERTATION WORK :
Formulation Development and Evaluation of Immediate Release Levonorgestrel and Ethinyl Estradiol Tablets (Glenmark Generics Ltd., Formulation Development Department,
Navi Mumbai)
AREA OF INTEREST :
Formulation Research and Development (FR&D)
Drug Regulatory Affairs and Intellectual Property Rights
SYMPOSIUMS ATTENDED :
- Actively participated in 60th Indian Pharmaceutical Congress, 2008, Delhi
- Actively participated in 3rd IPA-APTI State Level Convention-2008, Berhampur
- Actively participated in APTI-13th Annual National Convention-2008, Bilaspur
- Actively participated in 1st OPA state level convention-2010,Berhampur

[Guest]

hello sir/madam

i m post graduate in Drug Regulatory Affairs (M.Pharmacy) From MD, University, rohtak, seeking jpob in Drug Regulatory affairs.























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[vinitdabholkar]

Respected sir,
I'm writing to express my interest in the field of regulatory affairs. I am interested in an entry level position with your Company. I have heard that Brawn Labs Ltd holds an outstanding position in market , it will be a great opportunity for me to work with your organisation.
Experience has taught me how to build strong relationships with all departments at an organization. I have the ability to work within a team as well as cross-team. I have a thorough experience in both parentrals and orals related department.I have also faced audits like TGA January 2010,MHRA,ANVISA, customer audit- Novartis,GSK.
I am sending you my CV.
CURRICULUM VITAE
MR. VINIT V. DABHOLKAR
Email : vinit.dabholkar AT rediffmail.com / vinitdabholkar AT gmail.com
________________________________________
CAREER OBJECTIVE :
To work in a competitive and technological advanced atmosphere, realizing the goals of the company and in the process advancing my career.
EDUCATIONAL QUALIFICATION :
Degree University/ College Year Percentage
M. PHARM (Pharmaceutical Chemistry) Sinhgad College of Pharmacy, Off Sinhgad Road, Vadgaon (Bk.)
Pune - 411 041
Maharashtra.
Pune University, Pune. 2006-2008 First class
B. PHARM Sinhgad College of Pharmacy, Off Sinhgad Road, Vadgaon (Bk.)
Pune - 411 041
Maharashtra.
Pune University, Pune 2002-2006 Higher second class

PROFESSIONAL EXPERIENCE :
Company : Micro Labs Goa June 20ll till date
Strides Arco Lab (Onco Therapies Ltd.), Bangalore
[Sterile Manufacturing Facility] From May 2009 to June 2011
Job Responsibilities :
Current work profile :
Process validation execution and report preparation
Work Profile in Strides Arco Lab (Onco Therapies Ltd.)
1) IPQA
Manufacturing facility for the following dosage units :
- Liquid Injection
- Lyo powder for Injection

2) Media fill BMR preparation and Execution
3) BMR preparation & review
4) SOP preparation and review
5) Process validation protocol preparation,
6) Process validation execution and report preparation
Audit Faced :
1) TGA Audit : January 2010
2) MHRA Audit
3) ANVISA
4) Customer Audit – Novartis, GSK, Pfizer
RESEARCH TOPIC :
“Total Microwave Based Synthesis of Novel Condensed Pyrimidine Analogs of Gefetinib.
- Familiar with Gewald Synthesis
- Synthesis of chloroacetonitrile use for the cyclization of o-aminoesters.
- Cyclization reaction of o-aminoesters under acidic condition by passing Dry HCl gas etc.
INSTRUMENTS HANDLED :
- UV/visible Spectrophotometer Jasco V-530
- FTIR Spectrophotometer Perkin Elmer spectrum BX2
- QSAR using Cerius2, Insight II and TSAR (Accelrys)
INDUSTRIAL TRAINING :
Completed one month industrial training at Uni-sankyo Ltd., Lote MIDC,
Chiplun.
ADDITIONAL QUALIFICATION :
- Done Basics in Computer Application
AREA OF INTEREST :
- Quality assurance
- Regulatory Affairs
OTHER PURSUITS :
Poster presentation
At 59th Indian Pharmaceutical Congress, Dec. 2007
Title :
Novel microwave based synthesis, Biological evaluation and 3D QSAR of thienopyrimidine analogs of gefetinib as anticancer agents.
Authors : V. V Dabholkar*, M. S. Phoujdar, K. S. Jain et al
Research Article :
A Novel Microwave Assisted Green Synthesis of Condensed 2-Substituted Pyrimidin-4(3H)-ones Under Solvent Free Conditions.
(Published in Journal of Heterocyclic Chemistry)