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"우리가 꿈꾸는 성공은 대개 혼란과 무질서라는 토대에서 세워진다.
성공 이후에는 깔끔하게 정돈된 모습만 드러나기 때문에 우리가 잘 알기 어려울 뿐이다. "
by 팀 하포드
혼돈을 두려워말고 혼돈 속 기회를 찾는 것, 메시(messy)
그것이 바로 2017년, 혁신의 시작이다.
A detail-oriented, sincere and hardworking individual with a Master of Science and Over Fourteen years of GLP/GMP work experience
Expert in Audit trails review in Empower, Lab solutions, Tiamo and other softwares.
Experience in theoretical and practical knowledge in calibration, preventive maintenance, troubleshooting and problem solving of critical equipment like HPLC, GC, Auto Titrator,DR and UV-Spectrophotometer etc.
1. KRISHTEE SINGH PARIHAR
Mobile No.-8962702407 E-Mail:pharmakrishtee@yahoo.co.in
CAREER OBJECTIVES
To work as a TEAM so as to accomplish Organizational and Personal goals.
PROFESSIONAL SYNOPSIS
About 3 year of professional experience pertaining to the activities for Development Quality Assurance for
Domestic and ROW market.
Expertise on review of R&D Document and design of compliance report.
Presently Working with Plethico Pharmaceuticals Ltd as an officer- Development Quality Assurance.
Worked as Assistant Chemist-Quality Assurance with IPCA Laboratories Limited, Indore for about 1 Year.
Possess excellent communication; inter personal and problem solving skills with the ability to work in multi-
cultural environment.
Successful faced third party audit (MERCK, ABOTT) for formulation and development.
Exposure of audits like WHO, DSIR, ISO, customer audits, corporate audits and internal audits etc.
WORK EXPERIENCE
Officer Development Quality Assurance M/S Plethico Pharmaceuticals Ltd., Indore (MP)
(From September-2013 to Present)
Design and review of Standard operating procedure for Research and Development Department.
Review of stability protocol for adherence to the regulatory requirements.
Review of stability compilation data and Product Release report.
Review of Product development report (PDR) and standard testing procedure for various pharmaceutical
dosage forms.
Monitoring GMP & GLP compliance.
Issuance of documents (i.e. LNB, Raw data sheet, Calibration format, BIN Card, Change Control From, Deviation
Form etc.) related to F&D and ADL.
Review of Bill of raw material (BOM), Master Formula Card (MFC), LNB and Validation protocol.
Management of monthly Training programme at R & D Department.
Co-ordination with scientist for documentation related issues, also coordinate with CQA & Plant QA.
Coordination for design of compliance report for audit observation.
Software handing: SAS, JDE.
Assistant Chemist- Quality Assurance M/S IPCA Laboratories Limited, Indore (MP)
(From September-2012 to August 2013)
BPCR issuance, receipt, controlled copies issuance/withdrawal.
Review of BPCR.
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2. Controlling of Master copy of MPCR and Specification Record.
Data collection and preparation of Annual product review.
Project Associate-Process Development Lab Ranbaxy Laboratories Limited, Dewas (MP)
(From April 2011-September 2011)
Process validation of immediate release dosage form with the help of senior scientist.
Project Associate ADL Department Plethico Pharmaceutical Limited, Indore (MP)
(From November 2010 to March-2011)
Development activity of immediate release tablet formulations.
Comparative multimedia dissolution study of solid oral dosage form.
ACADEMICS
M.Pharm. (Pharmaceutics) from Shri Satya Sai College of Pharmacy, Sehore, Rajiv Gandhi Proudyogiki
Vishwavidyalaya, Bhopal (M.P), 2011 with 74.31%.
B.Pharm. from Pt. Ravishankar Shukla University, Raipur, Chhattisgarh, 2009 with 65.68%.
HANDS ON EXPERTISE
JD, SAS Programming and MS-Office
PERSONAL DETAILS
Date of Birth : 24th
Nov.1987
Father’s Name : Mr. A .P. Singh Parihar
Mother’s Name : Mrs. Sandhya Singh
Nationality : Indian
Marital Status : Single
Languages Known : English, Hindi
Permanent Address : House Number 100, Banganga road, Behind Mahendra Agencie,
Infront of Patel Hostel Shahdol M.P., (India)
REFERENCES
Available on request
DECLARATION
I hereby declare that the information given above is correct to the best of my knowledge.
Date Signature
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