Pulkiit parikh
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This document contains a summary of qualifications and work experience for Parikh Pulkit D, who has over 4 years of experience in quality assurance for pharmaceutical companies. He has a M.Pharma in Quality Assurance and a B.Pharm degree. His experience includes ensuring cGMP compliance, conducting audits, handling deviations and complaints, document review, and participating in validation activities. He is currently an Executive in QA at Jai Pharma and seeks to use his skills and knowledge in a well-established pharmaceutical company.
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Shyam KSG has over 20 years of experience in quality assurance for pharmaceutical companies. He currently works as an Associate Director of Quality Assurance at Agila Specialties, where he oversees quality compliance and systems. Prior roles include executive roles in quality assurance and quality control. He has expertise in aseptic processing, validations, compliance with regulatory agencies like USFDA and MHRA, handling audits, and leading cross-functional teams.
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Margesh J. Shah is seeking a position in the pharmaceutical industry utilizing her MS in Pharmaceutics and experience as a QC Chemist and Pharmacy Supervisor. She has over 10 years of experience in quality control and assurance testing pharmaceutical products and raw materials to ensure compliance with FDA regulations. Her technical skills include performing tests and analyses using instruments such as HPLC, UV-Vis spectroscopy, and dissolution apparatus.
Resume Anurag
Anurag Tiwari is a Junior Manager in Quality Assurance at Caprihans India Ltd in Nashik with over 7 years of experience in quality assurance in the pharmaceutical industry. He has worked at multiple companies, including Cipla, Wockhardt, and Caprihans. His responsibilities include ensuring compliance with quality measures through documentation, conducting audits, developing standard operating procedures, and supervising manufacturing processes to ensure regulatory compliance. He has expertise in areas like quality management systems, training and development, process validation, and product quality reviews.
Vipul Patel
Vipul Patel has over 20 years of experience in pharmaceutical quality control and laboratory management. He is currently an Associate Director of Laboratory Operations at Sun Pharmaceutical Industries in Detroit, Michigan, where he oversees quality control, analytical development, stability testing, and other laboratory functions. Patel has extensive experience ensuring regulatory compliance, leading inspections, and driving continuous improvement in laboratory operations.
MADHUKUMAR GOWDRU Updated
Madhukumar Nerlige Gowdru has nearly 8 years of experience in quality assurance roles in the FMCG and food & beverage industries. He is currently the Manager of Quality Assurance at Dairy Classic Ice Cream Pvt. Ltd., where he is responsible for quality audits, ensuring regulatory compliance, process improvements, and team management. Prior to this, he held quality assurance roles at SABMiller India Ltd. and Hindustan Coca-Cola Beverage Pvt. Ltd., where he improved product quality scores and reduced waste. He has extensive experience in quality control, auditing, regulatory compliance, and people management.
CV Ejaz - 2016
Ejaz Shahid has over 30 years of experience in pharmaceutical quality assurance and quality control. He holds a Master's degree in Pharmacy and has worked in senior QA roles for several pharmaceutical companies in Saudi Arabia, Pakistan, and the UAE. Currently he is the Senior Manager of Quality Assurance at Global Pharma in Dubai, where he oversees QA, QC, validation, auditing and ensures compliance with cGMP regulations.
Hitesh Maheshbhai Patel
Hitesh Patel has over 3 years of experience in the pharmaceutical industry working in quality assurance and quality control roles. He holds a Master's degree in Pharmaceutical Science from the University of Greenwich in the UK and a Bachelor's degree in Pharmacy. Currently he works as a Senior Quality Assurance Officer at Famycare Ltd in Ahmedabad, India where he is involved in validation activities, documentation review, and audits. Previously he worked at Nirlife Healthcare as a Quality Assurance Officer where his responsibilities included batch record review, deviation handling, and pre-dispatch inspections.
Cv mvv-nandakumar
M.V.V. Nanda Kumar has over 25 years of experience in quality control, quality assurance, regulatory affairs, research and development, and production in the pharmaceutical industry. He has extensive experience ensuring regulatory compliance and successfully completing audits from agencies like USFDA, MHRA, and EDQM. Nanda Kumar holds an MBA in Total Quality Management and has authored over 27 Drug Master Files submissions to various regulatory agencies. He is currently seeking a position where he can apply his skills and experience to improve quality systems and processes.
Resume-vipul patel
Vipul Patel is seeking an entry-level position in quality control where he can utilize his technical skills and experience. He has over 15 years of experience as a quality control chemist in pharmaceutical and food testing laboratories, handling instruments like HPLC, GC, and AAS. He has a Bachelor of Science degree and qualifications in computer applications and quality assurance systems.
Tarek-CV
A.F.M Tarek is seeking a challenging position in quality assurance where he can utilize his skills and experience. He has over 7 years of experience in quality assurance roles at pharmaceutical companies, ensuring compliance with cGMP guidelines and preparing for regulatory audits. His resume outlines his educational background in pharmaceutical science, work history managing quality systems, and track record of contributions and achievements across multiple employers.
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- 1. Parikh Pulkit D, M.Pharm (QA) Address: 39, Ganesh Park, Nr. Shayona city, R.C Tech. Road, Ghatlodia, Ahmedabad-380061. Telephone: 9662052330 (M), 8264254348 (M), 07927662509 (R) E-mail: parikhpulkit09@gmail.com CAREER GOAL To work in Quality assurance department in well-established pharmaceutical company, where I can use my knowledge and skills at there best ability. SUMMARY OF QULIFICATION Remarkable experience in Quality Assurance and Handling of various Quality Audits Proficiency in MS Office, SAP, Internet surfing Thorough knowledge of GMP regulations, protocols and SOPs Strong attention to details, Good interpersonal skills, excellent written and oral communication skills EDUCATION PROFESSIONAL APPOINTMENTS 4 Years & 1 Month of Total experience in Qaulity Assurance- Injectable Executive in QA at JAI PHARMA LIMITED- Mylan Lab. Group Company (Previously known as FAMY CARE LTD.), From Apr - 2015 to Present Executive in QA at INTAS PHARMACEUTICAL LTD., From Apr - 2014 to Apr-2015 Sr.Officer in QA at INTAS PHARMACEUTICAL LTD., From Jan - 2013 to Apr-2014 Tr. Officer in QA at INTAS PHARMACEUTICAL LTD., From Jan - 2012 to Jan-2013 Tr. Officer in QA at NIRLIFE HEALTHCARE LTD., From July - 2011 to Jan - 2012 Examination/ Degree Board/ University Year completed Passing class M.Pharma (Quality Assurance) NIMS University, JAIPUR 2009-2011 FIRST B.Pharm RGUHS, KARNATAKA 2004-2008 FIRST H.S.C. G.S.H.E.B 2004 FIRST S.S.C. G.S.E.B. 2002 DISTINCTION
- 2. JOB RESPONSIBILITY Executive-QA at JAI PHARMA LIMITED- Mylan Lab. Group Company • Ensure cGMP compliance during Different activity in plant • Responsible for line clearance, In-process checks, sampling in manufacturing and packing • Identification of GAP in Process & SOP and highlighted to QA manager and Revised it through raising Change control • SOP preparation related to IPQA. • Responsible for handling of Deviation & Market Complaint, Investigate and report it • Document Review • BMR & BPR Review • Participate in Validation Activity going in a Shop-floor • Submission of BMR & BPR to Doc-QA for its submission to Party • Communicate with Various other Department for smooth Functioning Executive-QA at INTAS PHARMACEUTICAL LTD. • Ensure cGMP compliances & responsible for Line clearance, In-process & surprise checks in all department store, formulation and packing • Assure Quality of product maintain during Batch manufacturing, Filling & sealing • Ensure all operation performed on shop floor as per SOP • Identify any non-compliance at various stages & ensure that there is no effect on product quality & treating such things with deviation • To check material requisition slip • Withdrawal & Handling of QC sample, sterility sample, retained sample, ADC sample, QP sample • Ensure online batch record • Facing & handling of International audits • Raise Vendor complaint in-case of any material with OOS observed and fill vendor complaint form with required information and preliminary investigation and forward complaint to CQA department • Investigation of product related market complains • BMR & BPR Review and its final submission to Doc-QA • Responsible for Issuance of various production records • Log books verification of all departments • Ensure Preventive Maintenance of equipment and its verification against plan • Perform SAP related QA transaction • Responsible for non-viable particle count monitoring and preparation of its report • Responsible for performing AQL • Actively participate in various validation activities and also in media fill • Co-ordination with Various other departments for smooth functioning Tr. Officer-QA at NIRLIFE HEALTHCARE LTD., • Stability Analysis of Drug Product for physical and chemical test as per ICH Guideline • Preparation and Review of Stability Protocol • Review of Batch Manufacturing and Batch Packing Records • Provide Stability related documents to Regulatory Department for preparing dossiers and also assist them in solving queries related to stability. • Handling of Instruments: HPLC, IR Spectrophotometer, U.V spectrophotometer AUDIT EXPERIENCES: USFDA, MHRA, ANVISA, TGA, Various Party Audits
- 3. PERSONAL DETAILS: Date of Birth: 15 th March 1987 Nationality: Indian Laugages known: English, Gujarati and Hindi Marital Staus: Married Hobbies: Travelling, Listing Music and playing cricket