Deputy Manager QA, working exp in beverage, juice water , sauces ketchup, mayonnaise and Jam & new product development. FSMS , HACCP & FSSC implementation& auditing
Ranjeet Singh has over 8 years of experience in quality assurance, food safety management systems, and auditing third party vendors. He holds an M.Sc. in Biochemistry and has worked in roles of increasing responsibility at several food and beverage companies. His experience includes implementing and auditing quality management systems, developing standard operating procedures, conducting supplier and product audits, and ensuring compliance with regulatory standards. Currently, he is seeking a position that allows him to continue learning and applying his skills in a growing organization.
Mohammad Imam Hossain has over 15 years of experience in quality assurance and food safety roles. He holds a Master's degree in Food Safety and Control and a Bachelor's degree in Agriculture. His experience includes implementing food safety systems like SQF, developing HACCP plans, conducting audits, ensuring compliance with food safety standards, and responding to customer complaints. Currently he works as a Quality Assurance Senior Food Technologist and SQF Practitioner at QST Ingredients and Packaging, where he helped the company achieve SQF certification and developed their HACCP plans.
Manish Kumar, B.sc-with Microbiology, chemistry, Diploma in dairy Technology.
Having 7 year Experience in Quality assurance in Food & Beverages (snacks, Tea, Water, Juices, Process food, staple foods- spices, flour, Oil and fats).Currently working with TATA global beverage ltd (TATA TEA LTD) in Tea manufacturing plant, handing Quality team. Handling Documentation part like-SOP preparation, change control, deviation control, process validation, IQ, PQ, OQ, System validation, Internal and external audit, Glass policy, Root cause analysis, CAPA, Trainings on GMP, Food safety, PRP, OPRP, HACCP, FSMS, 5S, Pest control management, customer complaint handling, Implementation of FSSAI norms, New product development, R&D in process and staples foods, Vendor management, Regulatory requirements as per FSSAI etc. Handled Microbiological, Analytical testing & Packing Exp, pasteurisation, homogenization, Fumigation in food and dairy industry, Handling team 20 Persons, sensory evolution of food products, SAP software handling, Yellow belt in lean six sigma.
Dairy experience- standardization of milk, pasteurization, homogenization, poly pack of full cream, tond, double tond milk, yogurt, spry drying milk power , nutritional protein powder, Ice-cream manufacturing.
The document is a resume for Mira B. Miguel summarizing her work experience and qualifications. She has over 7 years of experience in quality assurance functions, including experience implementing quality management systems and food safety programs. Currently she works as a Quality System Specialist for Wrigley Philippines Inc. where her responsibilities include auditing, supporting quality management programs, and serving as the company's liaison to government agencies. She has a degree in Chemical Engineering and is knowledgeable in quality standards including ISO 9001 and food safety systems.
10 Principles of Good Manufacturing Practice (GMP)Arrelic
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The document discusses the 10 principles of Good Manufacturing Practice (GMP). It explains that GMP establishes minimum standards for manufacturing products to prevent issues like contamination. Following the 10 principles can help make GMP a lifestyle at companies. The principles include having written procedures, carefully following procedures, documenting work, validating systems, facility and equipment design, maintaining facilities/equipment, job competence, cleanliness, controlling processes, and conducting audits. The document provides details on each principle and how following them helps ensure quality, compliance and safety.
The document provides a resume for Frank Vegeo Datilesespinosa, outlining his work experience in research and development roles for cosmetics and chemical companies over the past eight years, developing new products, evaluating raw materials, and ensuring quality control, as well as his educational background in chemical engineering technology. He possesses skills in product development, laboratory analysis, process development, and quality assurance systems.
G.V.S. Ratna Kumar is seeking senior level positions in production, quality, regulatory, research and development with chemical and pharmaceutical companies. He has over 20 years of experience in these areas and most recently worked as the Senior Manager of Production at Malladi Drugs and Pharmaceuticals Limited. He has extensive knowledge of quality standards, cGMP compliance, audits, documentation, and production planning.
This document provides definitions and descriptions related to Good Manufacturing Practices (GMP) regulations for pharmaceutical manufacturing. It defines key terms like active pharmaceutical ingredient, batch, and validation. It describes GMP requirements for facilities, equipment, documentation, personnel training, hygiene practices, and prevention of cross-contamination. The goal of GMP is to ensure manufactured products are safe, pure and effective.
This candidate has over 9 years of experience in quality control and assurance for vaccines and pediatric food products. Their skills include microbiological analysis, audits, biochemical analysis, and validation studies. They are proficient in techniques such as ELISA testing, sterility testing, and microbiological identification. They have a successful track record of implementing quality standards and process improvements to optimize efficiency and product quality.
Quality Assurance and Quality Management ConceptsVivek Jain
油
This document provides an overview of key concepts in pharmaceutical quality assurance and quality management, including the relationships between quality assurance (QA), quality control (QC), and good manufacturing practices (GMP). It defines QA, QC, and GMP and explains their roles and responsibilities. QA is a system that ensures products meet requirements, incorporating GMP and other factors. QC is the system for testing samples to maintain standards. GMP covers all production aspects to minimize risks and ensure quality, safety, and efficacy. Together, QA, QC and GMP work to consistently produce pharmaceuticals that meet quality standards.
Current good manufacturing practices and current good compounding Areej Abu Hanieh
油
The document discusses current good manufacturing practices (cGMP) regulations established by the FDA to ensure minimum quality standards for drug products. It covers cGMP requirements for facilities, equipment, components, production processes, packaging, labeling, quality control, audits and more. The regulations aim to help manufacturers produce safe and effective pharmaceuticals for patients.
The document discusses the importance of written procedures, records, and quality control processes for ensuring Good Manufacturing Practices (GMP) compliance. It emphasizes that written procedures provide clear guidance, consistency, and help attain high quality standards. Maintaining thorough records is also essential as they document the manufacturing process and can be referenced in the event of complaints. The key aspects discussed are performance, pride in one's work, and having proof through documentation to demonstrate GMP compliance.
This document provides an overview of Good Manufacturing Practices (GMP) for pharmaceutical manufacturing. It defines GMP as ensuring products are consistently manufactured and controlled to quality standards for their intended use. The document outlines key aspects of GMP, including facilities and equipment qualification, training, documentation, production and process controls, packaging and labeling, quality testing, and distribution. It explains that GMP is important for producing safe, effective drugs and minimizing risks that cannot be detected through final testing alone. International GMP guidelines from organizations like WHO, FDA, and ICH are also referenced.
This document provides a CV for Muhammad Anwar summarizing his professional experience and qualifications. He has over 15 years of experience in quality control and assurance roles in the food industry, specializing in dairy products. Some of the companies he has worked for include Nestle Pakistan, Hico Pak Ice Cream, and AZFPCo in Azerbaijan. His responsibilities have included new product development, quality testing, laboratory management, and production supervision. He holds various technical certifications and has participated in numerous training programs related to food safety, quality management, and processing techniques.
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.
The document discusses Good Manufacturing Practices (GMPs) and Hazard Analysis Critical Control Point (HACCP). It explains that GMPs and HACCP are important food safety systems used in the food industry. HACCP involves identifying potential hazards at critical control points in the manufacturing process and establishing procedures to monitor and control these hazards. The document provides details on the seven principles of HACCP and outlines critical control points in glass manufacturing as an example. It emphasizes that following GMPs and having standard operating procedures are important foundations for an effective HACCP program.
This document contains a resume for M. Saminathan, who has over 16 years of experience in quality, research and development roles in the chemicals and plastics industries. He holds a Master's degree in Chemistry and has worked in various positions related to quality assurance, product development, and laboratory management. His skills include experience with analytical instruments, ISO standards, process improvement tools, and product development from concept to commercialization.
The document outlines principles of good manufacturing practice (GMP) for quality management in a pharmaceutical manufacturing setting. It discusses nine key areas: quality management, personnel, premises and equipment, documentation, production areas, quality control, contract manufacturing, complaints and product recall, and self-inspection. For each area, it lists basic requirements and considerations to ensure consistent and quality production of pharmaceutical products according to regulatory standards.
I am seeking to obtain a position with a progressive, large international company or organization offering responsibility, advancement& individual growth.
To find a career opportunity that would utilized abroad range of my experience
To work in a dynamic & corporate environment, which will enable me to apply my expertise and problem solving skills, gained through advanced tertiary qualifications, work experience & international accreditations, to the best benefit of organization thereby achieving symbiotic growth
David O'Halloran has over 15 years of experience in quality assurance and regulatory roles in the pharmaceutical industry. He has held positions such as Director of QA/QC, Quality Assurance Supervisor, and Quality Assurance Associate. He currently works as an independent quality and regulatory consultant helping companies obtain production licenses from Health Canada.
Sreenivasu Vemulapalli is seeking a senior role in food safety, quality assurance, or regulatory compliance. He has over 18 years of experience in these areas, currently serving as Associate Vice President of Quality and Food Safety at The Global Green Company. His experience includes ensuring compliance with various global food safety standards and regulations.
M.S.R.Krishna Yadav has over 5 years of experience as a microbiologist. He currently works for FirstSource Laboratory Solutions LLP, where he conducts analysis of food, water, and drugs according to national and international standards. His responsibilities include performing tests accurately according to protocols, maintaining laboratory documents and equipment, and participating in inter-laboratory comparisons. Previously, he worked for NCMSL and Heritage Foods in roles involving the microbiological analysis of various agricultural commodities and water. Krishna Yadav has an M.S. in Food and Nutritional Science and a B.Tech in Biotechnology. He is proficient in microbiological techniques and computer skills.
Enoch Barde has over 8 years of experience in quality control and chemical analysis in the pharmaceutical industry. He has worked in roles such as quality control analyst, quality control officer, and R&D chemist. He is skilled in analytical techniques like HPLC and proficient in GMP, quality management systems, and computer programs like Microsoft Office.
Robert Sereno has 10 years of experience in food safety, quality assurance, and laboratory management. He holds a B.S. in Chemistry and seeks a managerial position where he can utilize his scientific background and communication skills. Sereno has a proven track record of implementing food safety systems, analyzing process data, and leading laboratory operations and staff.
Neslie Rebares is seeking a position where she can utilize her management, quality assurance, and production control experience. She has over 10 years of experience in quality assurance, documentation, regulatory affairs, and production supervision roles. Her educational background includes a Bachelor's degree in Food Technology. She is looking to join a dynamic team where she can continue her professional and personal growth.
Master of Good Manufacturing Practice - Course Detailsutspharmacy
油
Staff who hold postgraduate degrees in Good Manufacturing Practice (GMP) are essential for many pharmaceutical, biologic, medical device and food manufacturing companies.
This presentation provides an overview of the Master of Good Manufacturing Practice offered at the University of Technology, Sydney (UTS) in Australia. For more information visit www.gmp.uts.edu.au
This document provides a summary of Manoj Kumar Parida's professional experience and qualifications. It lists his current role as Senior Manager of Quality Control (Microbiology) at Emcure Pharmaceuticals Ltd. It then outlines his 16 years of experience in microbiology roles at various pharmaceutical companies. The document details his responsibilities in directing microbiology laboratories and ensuring compliance with regulatory standards.
This document contains the resume of Sudhanshu Tripathi, who has 6 years of experience as a Quality Executive in the food manufacturing industry. He has expertise in quality assurance, quality control, implementing food safety systems like HACCP and ISO 22000. He is seeking a role as a Quality Executive where he can oversee quality operations and ensure compliance with food safety standards. His professional experience includes roles at various food manufacturing companies where he was responsible for quality management, audits, supplier evaluation and ensuring product quality.
Pravin Ingle is seeking a position in quality assurance or quality control in the FMCG industry, preferably in Maharashtra. He has over 6 years of experience in roles such as quality control, quality assurance, food safety management systems auditing, and raw material/packaging material analysis. He is a lead auditor for ISO 22000:2005 and has experience implementing and auditing various management systems like ISO 9001, ISO 14001, and OHSAS 18001. He is proficient in SAP ERP systems and has a M.Sc. in Biotechnology.
This candidate has over 9 years of experience in quality control and assurance for vaccines and pediatric food products. Their skills include microbiological analysis, audits, biochemical analysis, and validation studies. They are proficient in techniques such as ELISA testing, sterility testing, and microbiological identification. They have a successful track record of implementing quality standards and process improvements to optimize efficiency and product quality.
Quality Assurance and Quality Management ConceptsVivek Jain
油
This document provides an overview of key concepts in pharmaceutical quality assurance and quality management, including the relationships between quality assurance (QA), quality control (QC), and good manufacturing practices (GMP). It defines QA, QC, and GMP and explains their roles and responsibilities. QA is a system that ensures products meet requirements, incorporating GMP and other factors. QC is the system for testing samples to maintain standards. GMP covers all production aspects to minimize risks and ensure quality, safety, and efficacy. Together, QA, QC and GMP work to consistently produce pharmaceuticals that meet quality standards.
Current good manufacturing practices and current good compounding Areej Abu Hanieh
油
The document discusses current good manufacturing practices (cGMP) regulations established by the FDA to ensure minimum quality standards for drug products. It covers cGMP requirements for facilities, equipment, components, production processes, packaging, labeling, quality control, audits and more. The regulations aim to help manufacturers produce safe and effective pharmaceuticals for patients.
The document discusses the importance of written procedures, records, and quality control processes for ensuring Good Manufacturing Practices (GMP) compliance. It emphasizes that written procedures provide clear guidance, consistency, and help attain high quality standards. Maintaining thorough records is also essential as they document the manufacturing process and can be referenced in the event of complaints. The key aspects discussed are performance, pride in one's work, and having proof through documentation to demonstrate GMP compliance.
This document provides an overview of Good Manufacturing Practices (GMP) for pharmaceutical manufacturing. It defines GMP as ensuring products are consistently manufactured and controlled to quality standards for their intended use. The document outlines key aspects of GMP, including facilities and equipment qualification, training, documentation, production and process controls, packaging and labeling, quality testing, and distribution. It explains that GMP is important for producing safe, effective drugs and minimizing risks that cannot be detected through final testing alone. International GMP guidelines from organizations like WHO, FDA, and ICH are also referenced.
This document provides a CV for Muhammad Anwar summarizing his professional experience and qualifications. He has over 15 years of experience in quality control and assurance roles in the food industry, specializing in dairy products. Some of the companies he has worked for include Nestle Pakistan, Hico Pak Ice Cream, and AZFPCo in Azerbaijan. His responsibilities have included new product development, quality testing, laboratory management, and production supervision. He holds various technical certifications and has participated in numerous training programs related to food safety, quality management, and processing techniques.
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.
The document discusses Good Manufacturing Practices (GMPs) and Hazard Analysis Critical Control Point (HACCP). It explains that GMPs and HACCP are important food safety systems used in the food industry. HACCP involves identifying potential hazards at critical control points in the manufacturing process and establishing procedures to monitor and control these hazards. The document provides details on the seven principles of HACCP and outlines critical control points in glass manufacturing as an example. It emphasizes that following GMPs and having standard operating procedures are important foundations for an effective HACCP program.
This document contains a resume for M. Saminathan, who has over 16 years of experience in quality, research and development roles in the chemicals and plastics industries. He holds a Master's degree in Chemistry and has worked in various positions related to quality assurance, product development, and laboratory management. His skills include experience with analytical instruments, ISO standards, process improvement tools, and product development from concept to commercialization.
The document outlines principles of good manufacturing practice (GMP) for quality management in a pharmaceutical manufacturing setting. It discusses nine key areas: quality management, personnel, premises and equipment, documentation, production areas, quality control, contract manufacturing, complaints and product recall, and self-inspection. For each area, it lists basic requirements and considerations to ensure consistent and quality production of pharmaceutical products according to regulatory standards.
I am seeking to obtain a position with a progressive, large international company or organization offering responsibility, advancement& individual growth.
To find a career opportunity that would utilized abroad range of my experience
To work in a dynamic & corporate environment, which will enable me to apply my expertise and problem solving skills, gained through advanced tertiary qualifications, work experience & international accreditations, to the best benefit of organization thereby achieving symbiotic growth
David O'Halloran has over 15 years of experience in quality assurance and regulatory roles in the pharmaceutical industry. He has held positions such as Director of QA/QC, Quality Assurance Supervisor, and Quality Assurance Associate. He currently works as an independent quality and regulatory consultant helping companies obtain production licenses from Health Canada.
Sreenivasu Vemulapalli is seeking a senior role in food safety, quality assurance, or regulatory compliance. He has over 18 years of experience in these areas, currently serving as Associate Vice President of Quality and Food Safety at The Global Green Company. His experience includes ensuring compliance with various global food safety standards and regulations.
M.S.R.Krishna Yadav has over 5 years of experience as a microbiologist. He currently works for FirstSource Laboratory Solutions LLP, where he conducts analysis of food, water, and drugs according to national and international standards. His responsibilities include performing tests accurately according to protocols, maintaining laboratory documents and equipment, and participating in inter-laboratory comparisons. Previously, he worked for NCMSL and Heritage Foods in roles involving the microbiological analysis of various agricultural commodities and water. Krishna Yadav has an M.S. in Food and Nutritional Science and a B.Tech in Biotechnology. He is proficient in microbiological techniques and computer skills.
Enoch Barde has over 8 years of experience in quality control and chemical analysis in the pharmaceutical industry. He has worked in roles such as quality control analyst, quality control officer, and R&D chemist. He is skilled in analytical techniques like HPLC and proficient in GMP, quality management systems, and computer programs like Microsoft Office.
Robert Sereno has 10 years of experience in food safety, quality assurance, and laboratory management. He holds a B.S. in Chemistry and seeks a managerial position where he can utilize his scientific background and communication skills. Sereno has a proven track record of implementing food safety systems, analyzing process data, and leading laboratory operations and staff.
Neslie Rebares is seeking a position where she can utilize her management, quality assurance, and production control experience. She has over 10 years of experience in quality assurance, documentation, regulatory affairs, and production supervision roles. Her educational background includes a Bachelor's degree in Food Technology. She is looking to join a dynamic team where she can continue her professional and personal growth.
Master of Good Manufacturing Practice - Course Detailsutspharmacy
油
Staff who hold postgraduate degrees in Good Manufacturing Practice (GMP) are essential for many pharmaceutical, biologic, medical device and food manufacturing companies.
This presentation provides an overview of the Master of Good Manufacturing Practice offered at the University of Technology, Sydney (UTS) in Australia. For more information visit www.gmp.uts.edu.au
This document provides a summary of Manoj Kumar Parida's professional experience and qualifications. It lists his current role as Senior Manager of Quality Control (Microbiology) at Emcure Pharmaceuticals Ltd. It then outlines his 16 years of experience in microbiology roles at various pharmaceutical companies. The document details his responsibilities in directing microbiology laboratories and ensuring compliance with regulatory standards.
This document contains the resume of Sudhanshu Tripathi, who has 6 years of experience as a Quality Executive in the food manufacturing industry. He has expertise in quality assurance, quality control, implementing food safety systems like HACCP and ISO 22000. He is seeking a role as a Quality Executive where he can oversee quality operations and ensure compliance with food safety standards. His professional experience includes roles at various food manufacturing companies where he was responsible for quality management, audits, supplier evaluation and ensuring product quality.
Pravin Ingle is seeking a position in quality assurance or quality control in the FMCG industry, preferably in Maharashtra. He has over 6 years of experience in roles such as quality control, quality assurance, food safety management systems auditing, and raw material/packaging material analysis. He is a lead auditor for ISO 22000:2005 and has experience implementing and auditing various management systems like ISO 9001, ISO 14001, and OHSAS 18001. He is proficient in SAP ERP systems and has a M.Sc. in Biotechnology.
Shivpal Baghel is seeking a position that utilizes his skills and promotes professional development. He has over 4 years of experience as a Quality Incharge in the biscuit industry. Currently, he works at Graintech Foods India Pvt. Ltd. ensuring product quality, food safety, and compliance with standards. His responsibilities include quality control, audits, customer complaint resolution, and staff training. He holds a B.Sc. and has experience operating laboratory instruments and conducting analyses.
The document provides a summary of the candidate's areas of strength, work experience, education, and skills. It highlights 7 years of experience in quality management and process improvement at PepsiCo, including managing quality systems, vendor management, and process enhancement. It also lists various quality and process improvement training programs attended and awards received for achievements like cost savings initiatives and productivity improvements.
Paul Joseph has over 25 years of experience in quality assurance and operations management roles in the food industry. He currently works as the Quality Assurance and Operations Manager for Nutritional Choice Australia, where he has helped establish quality systems and achieve growth for their export dairy business. Previously, he held quality assurance roles at several food manufacturers, demonstrating a track record of implementing food safety certifications and improving quality management systems.
Sumanraj is seeking a quality assurance role and has 4 years of experience in quality control, material inspection, and process improvement. He has expertise in techniques like HACCP, 5S, TPM, and OE. Sumanraj has a Master's degree in Microbiology and has worked at Hindustan Coca-Cola and Aachi Masal Foods in quality roles. At Hindustan Coca-Cola, he improved quality scores, implemented SMED for changeovers, and led water saving initiatives.
Ashish Kumar Mishra has over 9 years of experience in quality assurance and operations management. He is currently an Assistant Manager at Cargill India Pvt. Ltd., where he oversees quality assurance operations at three locations. He has expertise in implementing food safety and quality standards like HACCP, ISO 22000, and FSSC 2200. He also has a Green Belt certification in Lean Six Sigma and has received several awards for his work improving processes around recipe accuracy, moisture management, and inventory control.
The document provides a summary of Tarun's professional experience and qualifications. It outlines his over 5 years of experience in quality assurance and manufacturing excellence in the food industry, including current role as Quality Executive at Pernod Ricard India Pvt. Ltd. It also lists his education qualifications of a B.E. in Food Technology and certifications in areas like HACCP, Six Sigma and FSSC 22000. Key responsibilities and achievements from previous roles at companies like PepsiCo, Perfetti Van Melle are also highlighted.
The document is a curriculum vitae for Dr. Zakia Saeed, who has over 15 years of experience in pharmaceutical quality control, quality assurance, and regulatory affairs. She holds a PhD and MPhil in Pharmaceutical Chemistry from Karachi University. Her experience includes positions as Quality Control & Quality Assurance Manager at C.K.D Pharmaceuticals Pakistan and Senior Manager of Quality Assurance & Regulatory Affairs at Medisure Laboratories Pakistan, where she oversaw quality management, inspections, and regulatory compliance. She is skilled in methods validation, documentation, auditing, and ensuring compliance with cGMP standards.
Baidyanath Sah has 6 years of experience in quality management for the FMCG sector. He holds an MBA in Operations and Strategy and is a Lean Six Sigma Green Belt. At Dabur Nepal Pvt Ltd, he was responsible for quality assurance activities including sensory evaluation, HACCP, GMP compliance and ensuring products met quality standards. His experience includes quality audits, process validation, data analysis, hygiene monitoring and documentation. He is proficient in microbiological and chemical testing, effluent analysis, equipment calibration and HACCP verification.
Arra Nampally is currently an Assistant Manager at Sanofi India, with over 11 years of experience in quality control for pharmaceutical formulations. She has a Master's degree from Periyar University and a BSc from Osmania University. As Assistant Manager, she leads a team and is responsible for day-to-day operations of the quality control microbiology department to ensure goals are achieved. She has experience with audits, equipment qualification, method development and validation, and ensuring regulatory compliance.
The document is a curriculum vitae for S. Kalithas seeking a quality control or quality assurance role in the pharmaceutical or FMCG sector. It summarizes his over 10 years of experience in pharmaceutical quality control, including his current role as Deputy Manager of Quality Control at Biocon Ltd since 2008 where he manages a team of 8 members and oversees analytical work, documentation, and ensuring compliance. It also lists his educational qualifications including an MSc in Chemistry from Madurai Kamaraj University in 2003.
This document is a curriculum vitae for Ashvini Jaiswal. It outlines his work experience including his current role as a Technical Officer with the Food Safety and Standards Authority of India since 2016, previous roles as a Quality Officer with PepsiCo India Holdings from 2012 to 2015 and as an Executive Quality Assurance with Health Care Energy Foods from 2011 to 2012. It also lists his educational qualifications including an MSc in Food Technology from the University of Allahabad and training programs. His key strengths are listed as team leadership, risk assessment, hard work, and time management.
This document is a curriculum vitae for Ashvini Jaiswal. It outlines his work experience including his current role as a Technical Officer with the Food Safety and Standards Authority of India since 2016, previous roles as a Quality Officer with PepsiCo India Holdings from 2012 to 2015 and as an Executive Quality Assurance with Health Care Energy Foods from 2011 to 2012. It also lists his educational qualifications including an MSc in Food Technology from the University of Allahabad and training programs. His skills and strengths include food safety, auditing, inspection, and being a team leader.
Rahul Chavan is a quality assurance professional with over 9 years of experience in the food processing industry. He currently works as the QA and PD in-charge for Heritage Foods Ltd in Sangvi, India, where he oversees quality inspection, testing, documentation, and staff training. Previously, he held QA roles at various dairy and beverage companies where he implemented quality systems, conducted audits, and reduced operational losses. Chavan has a bachelor's degree in microbiology and certifications in quality management systems and auditing. He is seeking a responsible quality role where he can contribute to quality assurance.
Hi, I'm Ahmed, R&D Associate Scientist who loves to explore F&B trends. I recently developed a wide range of products in many categories ( juice, CSD, dairy, tomato products, jam,...), I'd like to combine my passion for research and innovation with the consumer needs.
01141305280
Bhavesh Patel has over 5 years of experience in quality assurance, quality control, and analytical method development using HPLC. He has a strong background in auditing and ensuring compliance with regulations from agencies like USFDA, WHO, and MHRA. His experience includes preparing SOPs, conducting audits, developing and validating analytical methods, stability testing, and serving as a training coordinator to ensure employees receive necessary GMP and GLP training. He has a M.Pharm in Pharmaceutical Chemistry and skills in statistical tools, instrumentation like HPLC and GC, method development and validation.
Commercial scale fermented dairy production unit.pptxmauryavikas465
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How can be fermented products produce in commercial scale, what are the problems faced by them and other various things about commercially fermented product like dahi, buttermilk, etc.
Italian vs. American Pizza 7 Key Differences and What Makes Each Unique.pdfallHungry
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Discover the 7 key differences between Italian and American pizza! From crust thickness to toppings and preparation, explore what makes each style unique. Whether you love authentic Neapolitan flavors or classic deep-dish indulgence, this blog breaks it all down.
WEEK-9-HM-ELEC-5PRODUCTION EQUIPMENT AND EQUIPMENT SELECTION.pptxtrishajhoyalmario
油
Selecting and purchasing food production equipment requires careful planning due to high costs and long-term impact. The process starts by identifying kitchen needs and determining equipment capacity for different areas. Next, various selection factors are considered, and equipment specifications (SPECS) are established. These SPECS are sent to suppliers for quotations, which are then evaluated before making a final purchase decision.
For equipment measured by volume
To ensure equipment can handle production needs, first determine the required production volume. Follow these steps for equipment measured by volume:
Estimate the number of portions needed per meal period using sales history.
Identify the portion size of each menu item.
Calculate total production quantity (portions portion size).
Consider the preparation method and total prep time.
Determine the number of batches based on prep method and timing.
Divide total production quantity by the number of batches to estimate equipment volume.
Consult manufacturer catalogs to select the best equipment for the establishment.
Call For research Articles.!!! Bioscience & Engineering: An International Jo...bioejjournal
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Call For research Articles.!!!
Bioscience & Engineering: An International Journal (BIOEJ)
ISSN : 2349 - 848X
webpage URL; https://airccse.com/bioej/index.html
Authors are invited to submit papers through the Journal Submission System.
https://airccse.com/submission/home.html
Submission Deadline; April 05, 2025
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Here's where you can reach us : bioej@airccse.com (or) bioejsecratry@yahoo.com (or) bioej@aircconline.com
Maintaining a well-balanced diet can be challenging, especially for those committed to plant-based nutrition. While a plant-based diet is rich in fiber, antioxidants, and essential nutrients, it can sometimes lack key vitamins and minerals like B12, iron, and omega-3s. Without careful planning, these gaps may lead to fatigue, weakened immunity, and nutrient imbalances that impact overall health. To ensure proper nourishment, individuals must incorporate a diverse range of whole foods, fortified products, and supplements that provide the necessary nutrients to thrive.
key companies:-
Taj hotels[IHCL]
Oberoi hotels and resorts
OYO rooms
Lemon tree hotels
tell me the industry size, growth rate and market potential.
market share of different companies.
STP strategy of top 3 companies.
1. Curriculum vitae
RANJEET SINGH S/O Kunwar singh
Ram jaipal path Baily road singh
Near Jalalur city gate
Danapur Patna 801503
Phone: 09164835017
Email:ranjeetsingh083@yahoo.com
Total Experience 9.0 Year FMCG/QA/QC, and food safety management
system implementation & Auditing of third party vendors & NPD
JOB OBJECTIVE
Setting suitable position that offers me and environment of learning and allows me
free freedom to be creative, to reach the point of perfection in a dynamic and growing
organization through my work in a synergic and growing organization through my
work and contribution.
EDUCATION/DEGREES
M.Sc. Biochemistry with 74% -2006 - 2008
P.G Diploma in Biotechnology with 64% -2005 - 2006
B.Sc. (Chemistry, Botany ) with 63% -2002 - 2005
SKILLS
QMS, HACCP, FSMS, FSSC ,TPM ,Kaizen& Six Sigma, Audit
Documentation, SOP,SPI, Program & Manual developments.
SAP , MS Office , & Hardware
PROFESSIONAL EXPERIENCE 9.0 year in FMCG
2. Current Status
Sublime foods Pvt. Ltd /India food park Pvt. Ltd (KA)
(Future Group)
Deputy Manager Quality Assurance.
Company Profile: An ISO 22000:2005 certifiedcompany. Name - Sublime Foods Pvt
Ltd (J.V of future group) India food park Tumkur Karnataka (Bangalore)
Brand Name Sangis kitchen & Tasty treat
Products Name Sauce, Ketchup, Jam, Mayo & spread
Supplierpartner of Big Bazaar & future group, Sangiskitchen
Job responsibilities:-
To ensure Quality (physical, chemical & microbiological) of product as per
committed Specifications at procurement, in process, Storage and dispatch.
Develop and ensure various test procedures necessary and required in order to
establish Quality of a products as per company and FSSAI requirements.
To develop and execute sampling plan and analysis plan for various product.
To ensure the quality of products at outsourced location as per standard.
To plan and Carrying out the supplier audit at existing and new vendorfacility for
ensuring proper quality of supplied products & lab equipments.
Ensure proper infrastructure and resource for developing and smooth functioning
of analysis and R&D lab activities on day to day basis.
To develop the new systems, infrastructure, resources as per management
requirements.
Development of new vendors for Raw & packaging materials.
To provide support and training to the QA personal and develop them as a team.
To implement, strengthen and improve Quality Management Systems and Food
Safety Management Systems.
To plan & execute internal Audits, food safety audits in order to enforce proper
SOP, documentation, GMP, GHP and GLP
To coordinate with External Laboratory for product testing and timely results.
To coordinate with statutory and regulation Agencies in order to system
compliances, support and guidance.
To actively initiate and participate in various NPD Projects and successfully
accomplish them with in timeframe.
3. Root cause analysis & CAPA .
MIS reports to the top management on daily basis.
Damyaa P.J Foods Pvt. LtdRampur U.P
August 2015 toMar- 16 as an AssistantManager- Quality Assuranceand
My job profile includes:
Create SOP, SPI & programs of all process system,
Developed HACCP & its validation & review critical control point.
Process validation & evaluate the problem in process which affects the quality of
product.
PRP, OPRP & CCP validation and focused on food safety.
Internal Auditing of each area of plant.
ISO22000 Documentation & systemimplementation.
Developed new product packaging and sensory evaluation to enhance product
quality .
Quality analysis of raw materials-
Physical, chemical analysis of raw materials and documentation as per the same.
Manage internal and external auditing of quality systems.
Provide qualitytrainingtoproductionemployees.
Trend analysis of all customer complaints and report to corporate.
Controlling the all aspects related to the quality and team handling.
Analysisof process systemandimplementsome new approachforbetterqualitywith
increase productivity.
Company Profile: An ISO 22000:2005 certifiedcompany.
Name P.J. FOODS
Brand Name 9AM, CHAT, PURE
Products Name Sauce,Ketchup,Noodles,Jam
Supplierpartner of Big Bazaar, Metrocash & carry ,PVRCinemas,Sbarro.
SAHARA Q SHOP UNIQUE PRODUCT RANGE LTD.GURGAON Package drinking
water Division (Natural & packaged drinking water).
30/AUG/2012 to 31 AUG 15
As Senior Executive- Food, 'Quality water Department
Vendor development & Plant Auditing
4. Quality auditing as per Quality norms and implement of PRP.CCP OPRP HACCP
GMP GHK and developed FSMS in vendor site.
FSSAI,ISO HACCP & CAPA GMP GHK and SOP & OPL
R.O membrane cleaning at low cost chemical.
Plant chemical & Microbial test validation.
Hot water CIP system Installation.
RM & PM testing as per standard
QA/QC testing of finished products on the basis of FMEA and QI.
CRC study & CCP & CP developments and monitoring
Microbiological testing of finished product.
Arrangement of Carbon media (ACF) send filter media & filter as per
requirement from genuine or specific Quality.
Validation of Carbon media.
Regulatory & statutory compliances as per FSSAI
Perform testing and validation of quality after filling.
VARUN BEVERAGE LTD. 6-FEB-2012 TO 28-aug-2012
As Process Quality executive & Quality Executive
Preparation of RAW & Ready Syrup.
Operation of tetra pak CIP & Dala Toffola
Operation of Beverage blanding like Mosonear , KHS ,contiflow (Krones) & Mass
bland (shipa).
Works on TPM & CRC control
Microbiological testing of water, juice and soft drink.
Raw & packaging material testing.
Bisleri International Pvt. Ltd New Delhi 4/Aug/2010 to 31-Jan-12
As Quality&ProductionExecutive
Material analysis of raw and packing material as per standard specification,
interacting of Quality issues, keeping records of analysis.
RM&PM Testing.
HACCP, PRP.OPRP Validation etc.
Production planning, shift handling and wastage control.
Enhance productivity, break down analysis.
Handling All Quality and Production Issue.
Control the CRC complains in product.
All Raw materials testing as per standard.
Maintain GMP/GHK /GHP TPM in Plant.
Control the break down and enhance Productivity.
5. Hindustan Coca Cola Beverage Pvt. Ltd | Dasna Ghaziabad U.P
(ISO22000:2005, 14001& PAS 220) 4/Mar/2009 to 4/Aug/2010
As Quality Executive
Follow effectively company's SOP, SPI and PROGRAM during working.
Ensure GMP, GHP, and TPM & FIFO system followed.
Maintain sanitation and hygiene standards as per the company's approved
Standard Sanitation and operating procedures (SOP) within production and
packaging section.
Responsible for reports of all Raw materials, packing material, finished product
testing & keeping records.
Ensuring uniformity in product quality. If deviation found take corrective action.
Handle customer complaints (CRC), root cause analysis of complaints, take
corrective action and records.
Ensure online quality analysis of Coca Cola product.
Establishment of process quality system-Help in development of process quality
monitoring scheme and cleaning plan.
Ensure compliance of laid down process parameters- recording in log sheets,
analysis of parameters and results.
Identification of cause and effects of process deviations, initiate corrective
measures and implement solutions.
I integrated pest management -demarcation of defenses' lines, determination
and use of pest control instrument (Glue traps, RBS, Spray guns etc.)
categorization and use of pesticides.
Sensory evaluation and release of materials and products-sensory panel
screening, conducting blind test to evaluate Performance, sensory of incoming
raw materials, intermediate and finished product as pre-requisite to quality
release and RM & PM.
OE PROJECT IN COKE
Reduced The CRC complains in finished Product In carbonated and non -
carbonated Beverage.
Enhanced the concentrate yield in RGB (Returnable Glass Bottle Beverage)
TRAINING UNDER TAKEN
10 Days QA training by DNV on ISO 22000:2005, PAS 220 AND FSMS. TPM, 7
QC TOOL, SIX - SIGMA, POKA- YOKE. KAIZEN.
3 Days Training on Domino inkjet coding machine AX300, AX 100.
4- Day Training on Krones Pet line 600bpm, Operation of countiflow and filler.
EXTRA CURRICULAR ACTIVITIES
6. Successfully streamlined SOPs, SPI, PROG, SPL, KIZEN, 7 QC TOOLS and Poka-Yoke
and implemented GMP, GHK/GHP, ISO, HACCP, FSMS,ISO, QMS Programs.
INDUSTRIAL INSTRUMENT HANDLING & OPERATION
Mojoneer, Paramix, ASEBI, EBI (Filtec), Krones EBI, Tunnel Pasteurizer, Dynatron
Bottle Washer,
Hilden Labeler, Anton par Co-Brix, Pu- Recorder, Domino coding Machine, Dead
Weight Calibration
Spectrophotometer, TDS Meter, PH-Meter, Torque tester,
RESEARCH WORK
INDIAN VATERNARY RESEARCH INSTITUTE (IVRI) Bareilly, Work on
identification of goat Vitronectin (ECM Protein) Binding S. Aureus Adhesions.
Extraction and Purification of Blood Clotting factors. ByDEAE-Sepharose ION
Exchange chromatography and Affinity chromatography.
LAB INSTRUMENT HANDLING `
SDS-PAGE Analysis, ELISA, Blotting Technique, Affinity Column
Chromatography, DNA Isolation, Plasmid Isolation, Silver Staining.
PCR AGRAOSE Gel electrophoresis. Rapid Microbiology Technique, protein
purification from Bacteria and its Binding Study.
ACTIVITIES & ACHIEVEMENTS
Actively participated in INTERNATIONAL SYMPOSIUM on Microbial Diversity
organized by S.B.A.M, R.D. University, M.P
Actively participated in MICROTECT-2005, Junior Scientist Award organized by
S.B.A.M, R.D. University, M.P
Participated In National workshop of Applied Molecular tools and technique.
Participated in Seminar, got first prize.
Hobbies
Reading & Traveling
LANGUAGE Known
Hindi, English
DECLEARATION
7. I hereby declare that the statements provided above are true to the best of my
knowledge and belief.
Date. Place.