Nguyen Trong Tan has over 10 years of experience in pharmaceutical research and development. He is currently an R&D Supervisor at OPV Pharmaceutical, where he leads projects developing new products and improving manufacturing processes. Previously he held roles with increasing responsibility at other pharmaceutical companies, including positions in production supervision and quality control. He has a Bachelor's degree in Chemistry and training in chromatography techniques.
This report provides comprehensive information on the current therapeutic developmental pipeline of Genzyme Corporations, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. It also reviews latest updates, and featured news and press releases, along with special features on late-stage and discontinued projects.
http://www.researchmoz.us/genzyme-corporation-product-pipeline-review-2015-report.html
Vinaykumar P Desai detail job profile- June-2015 for QA QC Technical service...Vinay Desai
Vinaykumar Desai is seeking a position in QA, QC, or technical services with his 28 years of experience in chemical analysis and analytical instrumentation. He currently works as a Technical Services Manager at a large Indian chemicals manufacturer, where he is responsible for product specifications, quality compliance, technical support, and training. Vinaykumar has extensive experience with analytical instrumentation and a strong background in quality systems, including ISO 9001 and the NABL accreditation process.
Pradeep Sarda is seeking assignments in pharmaceutical formulation development. He has over 10 years of experience in formulation and development of various dosage forms including tablets, capsules, and modified release formulations. He has worked at several companies, including IPCA Indore, Famycare Ahmadabad, and Mylan Laboratories. His experience includes preformulation studies, process development, scale-up, technology transfer, and generating documentation for product development and regulatory submissions. He has expertise in pelletization, granulation, compression, and coating processes. Pradeep holds an MPharm in Pharmaceutics and has handled various projects involving formulation of anti-malarial, contraceptive, and anti-Parkinson drugs.
Walid Mohamed Abd Elgelil Saleh is seeking a quality assurance position. He has over 10 years of experience in quality assurance roles for pharmaceutical companies. His experience includes ensuring compliance with GMP regulations, batch release, complaint handling, self inspections, training staff on GMP, and supplier evaluation. He has a Bachelor's degree in pharmaceutical science and is proficient in English and computer skills like Microsoft Office.
Sudeep Killedar is seeking a career enriching role in business development with a focus on the pharmaceutical industry, leveraging his nearly 9 years of experience in production, process enhancement, packaging, and research documentation for well-known pharmaceutical organizations. He has skills in enhancing production operations, optimizing resources, and ensuring compliance with quality standards and regulatory guidelines. The document provides details on his educational background and work experience in various roles with increasing responsibility in the pharmaceutical industry.
Pharmaceutical Industry Departments roles and responsibilities manasa life sc...ManasaLifeSciencesMa
Pharmaceutical Industry Departments and its roles and responsibilities were discussed. Product selection, Development, Manufacturing, Product approval, Marketing
This document provides an overview of Nutramedica Laboratories Sdn Bhd (NLSB), including its services, product development process, standard operating procedures, and regulatory requirements. NLSB is a GMP-certified manufacturer of herbal and plant-based personal care and health supplements. It assists clients with product formulation, certification, and testing. The document outlines the roles and responsibilities of NLSB's R&D staff and lab assistants. It also includes a list of services provided and pricing, as well as charts detailing the business and product development flows.
GMP and cGMP considerations ensure consistent manufacturing and quality control of pharmaceutical products. Key points:
1. GMP aims to minimize risks like contamination or incorrect dosing that cannot be eliminated through final testing.
2. QA, GMP and QC are interrelated but distinct - QA ensures overall quality, GMP covers all production aspects, and QC involves sampling, testing and release procedures.
3. Following GMP guidelines is important for safety, efficacy and export opportunities. GMP requires documented procedures covering all steps to build quality into every batch.
This report provides comprehensive information on the current therapeutic developmental pipeline of Genzyme Corporations, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. It also reviews latest updates, and featured news and press releases, along with special features on late-stage and discontinued projects.
http://www.researchmoz.us/genzyme-corporation-product-pipeline-review-2015-report.html
Vinaykumar P Desai detail job profile- June-2015 for QA QC Technical service...Vinay Desai
Vinaykumar Desai is seeking a position in QA, QC, or technical services with his 28 years of experience in chemical analysis and analytical instrumentation. He currently works as a Technical Services Manager at a large Indian chemicals manufacturer, where he is responsible for product specifications, quality compliance, technical support, and training. Vinaykumar has extensive experience with analytical instrumentation and a strong background in quality systems, including ISO 9001 and the NABL accreditation process.
Pradeep Sarda is seeking assignments in pharmaceutical formulation development. He has over 10 years of experience in formulation and development of various dosage forms including tablets, capsules, and modified release formulations. He has worked at several companies, including IPCA Indore, Famycare Ahmadabad, and Mylan Laboratories. His experience includes preformulation studies, process development, scale-up, technology transfer, and generating documentation for product development and regulatory submissions. He has expertise in pelletization, granulation, compression, and coating processes. Pradeep holds an MPharm in Pharmaceutics and has handled various projects involving formulation of anti-malarial, contraceptive, and anti-Parkinson drugs.
Walid Mohamed Abd Elgelil Saleh is seeking a quality assurance position. He has over 10 years of experience in quality assurance roles for pharmaceutical companies. His experience includes ensuring compliance with GMP regulations, batch release, complaint handling, self inspections, training staff on GMP, and supplier evaluation. He has a Bachelor's degree in pharmaceutical science and is proficient in English and computer skills like Microsoft Office.
Sudeep Killedar is seeking a career enriching role in business development with a focus on the pharmaceutical industry, leveraging his nearly 9 years of experience in production, process enhancement, packaging, and research documentation for well-known pharmaceutical organizations. He has skills in enhancing production operations, optimizing resources, and ensuring compliance with quality standards and regulatory guidelines. The document provides details on his educational background and work experience in various roles with increasing responsibility in the pharmaceutical industry.
Pharmaceutical Industry Departments roles and responsibilities manasa life sc...ManasaLifeSciencesMa
Pharmaceutical Industry Departments and its roles and responsibilities were discussed. Product selection, Development, Manufacturing, Product approval, Marketing
This document provides an overview of Nutramedica Laboratories Sdn Bhd (NLSB), including its services, product development process, standard operating procedures, and regulatory requirements. NLSB is a GMP-certified manufacturer of herbal and plant-based personal care and health supplements. It assists clients with product formulation, certification, and testing. The document outlines the roles and responsibilities of NLSB's R&D staff and lab assistants. It also includes a list of services provided and pricing, as well as charts detailing the business and product development flows.
GMP and cGMP considerations ensure consistent manufacturing and quality control of pharmaceutical products. Key points:
1. GMP aims to minimize risks like contamination or incorrect dosing that cannot be eliminated through final testing.
2. QA, GMP and QC are interrelated but distinct - QA ensures overall quality, GMP covers all production aspects, and QC involves sampling, testing and release procedures.
3. Following GMP guidelines is important for safety, efficacy and export opportunities. GMP requires documented procedures covering all steps to build quality into every batch.
Italy Coagulation Testing Market: Innovative Technologies and Emerging Busine...ReportsnReports
This report provides a comprehensive analysis of the Italian coagulation testing market, including 10-year volume and sales forecasts for 40 coagulation procedures. It reviews current coagulation instrumentation technologies and major suppliers, and provides business opportunities and strategic recommendations for companies. The 402-page report costs a single-user license of US$5400 and is available for purchase from the provided website. It contains in-depth analysis of the Italian market structure, key players, technologies, and growth opportunities in coagulation testing.
Copp- Certificate of Pharmaceutical ProductsDr. Jigar Vyas
The document provides guidelines for applying for a WHO GMP Certificate of Pharmaceutical Product (COPP) from the Indian drug regulatory authority, CDSCO. An application for a COPP must be submitted to the respective CDSCO zonal/sub-zonal office, along with documents like a product permission copy, notarized product summary sheet, and documentation of quality control procedures. CDSCO officers will inspect applicant sites to ensure compliance with WHO GMP guidelines before issuing a COPP, which certifies that a pharmaceutical product is manufactured according to proper standards for international distribution and registration.
Olympus impurity is a manufacturer and supplier of Budesonide impurities like Budesonide EP impurity A / 16α-Hydroxy prednisolone, Budesonide EP Impurity B, Budesonide EP Impurity C, Budesonide EP Impurity E / Budesonide Related Compound E / 14,15-Dehydro Budesonide, Budesonide EP Impurity F ...
Fawzy Saad Hassan has over 10 years of experience as a consultant for pharmaceutical, biopharmaceutical, and vaccine projects. He has established quality assurance systems, developed validation master plans, conducted technology transfers, and provided GMP training. He is the executive manager of an international consultancy center and has experience working with companies like GSK, Novartis, Sanofi Aventis, and VACSERA.
Yuanzhen Zhong is seeking a new position and has over 25 years of experience in product formulation and development across various industries including pharmaceutical, cosmetic, beverage, and polymer. He has a PhD in Physical Chemistry of Polymers and has held positions at companies like MonoSol Rx, Hartz Mountain, PepsiCo, L'Oreal, and ISP where he successfully developed new products and delivery technologies. He is looking to continue making contributions to new product development.
Founded in 1993, Galenix offers a complete range of services to the pharmaceutical and biotechnology industries. From early stage drug development to the registration, all development processes are performed within our state-of-the-art facilities.. Using a three-stage strategy, Galenix delivers:
-Our innovative Drug Delivery Solutions portfolio offers 6 technologies platforms for oral delivery: Microgix®, Minextab®, Minextab Floating®, Mucolys Film®, Mucolys Flash® and ODTx®.
- The Galenix Drug Product Development process offers customers complete, efficient control over all R&D activities including feasibility studies, API sourcing and characterization, preformulation, formulation, analytical development and validation, Regulatories affairs, consulting and Marketing Authorization Application (MAA) registration. Galenix has obtained more than 50 MAAs over 20 years.
- Galenix licensing-out innovatives Drug Product in OTC and RX Market for Europe, US and others country in the word.
Spécialités : Pharmaceutical Drug Delivery Systems; Drug Product Development and DP Licensing-out
Parveen Bhatarah has over 15 years of experience in pharmaceutical management, API development, drug substance manufacturing, technology transfer, and formulation development. They have successfully developed, scaled up, and manufactured a wide range of drug substances and formulations, and have transferred technologies for commercial manufacturing. Parveen also has experience evaluating and qualifying CMOs, building industry partnerships, and presenting scientific findings to regulatory agencies.
This resume summarizes the career experiences and qualifications of Mizanur Rahman. Over 5 years of experience in production roles at pharmaceutical companies including Mundipharma (Bangladesh) Pvt. Ltd. and Asiatic Laboratory Limited. Extensive skills in pharmaceutical manufacturing processes, quality control, instrumentation, and computer systems. Currently seeking a mid-to-high level position in production, quality assurance, or product development at a pharmaceutical company where he can apply his technical expertise and experience. Well qualified with a Bachelor's degree in Pharmacy.
Lee Anthony Joynston provides a curriculum vitae summarizing his personal details, skills, academic and professional experience. He received a BSc in Biochemistry from the University of Sheffield in 2006, and his third year project involved investigating and purifying the McrC gene product. Since 2013, he has worked as the Production Team Leader at DRFP SmartSeal Ltd, a medical device manufacturing company, where he supervises staff and ensures compliance with quality standards. He has strong communication, organization, and laboratory skills developed through his education and career.
Brian Lam is seeking a position as a QA officer. He has over 2 years of experience working as a QA officer for Bristol Laboratories in the UK where his responsibilities included sampling and testing materials, approving artwork, batch record reviews, audits, and validation activities. He also did a pharmacy clerkship with Watsons Ltd in Hong Kong. Brian has an MSc in Pharmaceutical Technology from the University of Bradford and a BSc in Pharmaceutical Science from the University of Manchester. He has strong technical skills and interpersonal skills.
The document discusses pilot plant scale up techniques for herbal extract formulation production. It defines key terms like pilot plant and scale up. The objectives of pilot plant studies are to produce stable products and identify critical process features. Personnel should have experience in both pilot plant operations and production. A review of the formula, raw materials, and equipment is important. Master manufacturing procedures are developed to guide scale up. Product stability studies ensure uniformity. A case study describes scale up of mangiferin extract from mango leaves from bench to pilot scale.
1. Devendra Singh Rathore is seeking a dynamic career in the pharmaceutical industry utilizing 8 years of experience in production, planning, packaging, and resource management.
2. He has worked as an Executive at Zyg Pharma since 2015 and as a Production Chemist at Osmed Formulation Pvt Ltd from 2012-2015 where he oversaw production and packaging operations.
3. Prior to that he worked as a Chemist at Super Pharma Products from 2008-2011 where he managed batch creation, planning, and packaging operations.
Mohamed Shawky is applying for a QC Manager position and has over 12 years of experience in quality control for pharmaceutical companies. He is currently the QC Manager at Western Pharmaceutical Industries where he manages quality control laboratories and ensures compliance. He has a Bachelor's Degree in Pharmacy and provides his contact information expressing interest in an interview.
The document provides a summary of Ms. Dulari H. Gupta's educational background and work experience in the pharmaceutical regulatory industry. It details her 17+ years of experience in regulatory affairs and quality assurance roles at various pharmaceutical companies. Currently, she works as the Manager of Regulatory Affairs at Glenmark Pharmaceuticals, where she leads the Middle East region and is responsible for regulatory submissions and responding to health authority queries. The document also outlines her responsibilities, achievements, skills, and references.
This document is a resume for Cory M. Zach that outlines his objective, education, and work experience. It summarizes that Zach has over 10 years of experience in quality assurance and regulatory roles within the life sciences industry. He holds an MBA from Webster University and a Bachelor's degree in Biological Sciences. Currently, Zach works as an R&D IT Product Specialist at Monsanto, where he is responsible for rolling out software platforms, collaborating with stakeholders, and identifying opportunities to expand platform usage and grow customers.
Mostafa Mohamed Nassar has over 20 years of experience in pharmaceutical production management, including sterile and non-sterile areas. He is currently the Production Manager at Grand Pharma in Egypt, where he helped start new production lines, develop quality systems, and increase productivity five-fold. Previously, he held production management roles at Adwia and Medical Union Pharmaceutical, where he helped start new sterile facilities and improve quality levels. He has a BSc in Pharmacy from Tanta University and extensive training in sterile manufacturing techniques.
This document contains the curriculum vitae of Mohamed Hosny Abo-samra. It includes his personal details, education history, employment history, training, courses, skills, and personal characteristics. His employment history includes roles as a Quality Control Engineer, Lab Chemist/Supervisor, QC Analytical Chemist, QC Chemist, and Medical Representative. He has a Bachelor's degree in Chemistry and Biochemistry from Alexandria University and specialized training and certifications in quality control, food safety, laboratory analysis, and English.
Tomislav Filipović has over 15 years of experience in laboratory management, sales, and production roles. He has a Bachelor's degree in Food Technology and has worked as a laboratory manager at KONMARKLAB Ltd. where he implemented quality assurance systems and methods validation. He also served as Director, managing business and accounts. Filipović held roles as a laboratory manager and sales representative at LABENA Ltd., and was a production technologist and shift leader at Roto Promet Ltd. His skills include Microsoft Office, English proficiency, and he holds a B category driver's license.
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.
This document discusses pilot plant scale-up techniques for pharmaceutical manufacturing. It defines a pilot plant and scale-up process. The key steps in scale-up involve conducting laboratory and smaller pilot studies, designing and constructing a pilot plant, evaluating results to make corrections, and deciding whether to proceed to full-scale production. General considerations for a pilot plant include personnel requirements, equipment, production rates, process evaluation, and ensuring product stability and uniformity. GMP must also be followed in areas like process validation and documentation.
This document discusses pilot plant scale-up techniques for pharmaceutical manufacturing. It defines a pilot plant and scale-up process. The key steps in scale-up involve conducting laboratory and smaller pilot studies, designing and constructing a pilot plant, evaluating results to make corrections, and deciding whether to proceed to full-scale production. General considerations for a pilot plant include personnel requirements, equipment, production rates, process evaluation, and ensuring product stability and uniformity. GMP must also be followed in areas like process validation and documentation.
This document discusses pilot plant scale-up techniques for pharmaceutical manufacturing. It defines a pilot plant and scale-up process. The key steps in scale-up involve conducting laboratory and smaller pilot studies, designing and constructing a pilot plant, evaluating results to make corrections, and deciding whether to proceed to full-scale production. General considerations for a pilot plant include personnel requirements, equipment, production rates, process evaluation, and ensuring product stability and uniformity. GMP must also be followed in areas like process validation and documentation.
Italy Coagulation Testing Market: Innovative Technologies and Emerging Busine...ReportsnReports
This report provides a comprehensive analysis of the Italian coagulation testing market, including 10-year volume and sales forecasts for 40 coagulation procedures. It reviews current coagulation instrumentation technologies and major suppliers, and provides business opportunities and strategic recommendations for companies. The 402-page report costs a single-user license of US$5400 and is available for purchase from the provided website. It contains in-depth analysis of the Italian market structure, key players, technologies, and growth opportunities in coagulation testing.
Copp- Certificate of Pharmaceutical ProductsDr. Jigar Vyas
The document provides guidelines for applying for a WHO GMP Certificate of Pharmaceutical Product (COPP) from the Indian drug regulatory authority, CDSCO. An application for a COPP must be submitted to the respective CDSCO zonal/sub-zonal office, along with documents like a product permission copy, notarized product summary sheet, and documentation of quality control procedures. CDSCO officers will inspect applicant sites to ensure compliance with WHO GMP guidelines before issuing a COPP, which certifies that a pharmaceutical product is manufactured according to proper standards for international distribution and registration.
Olympus impurity is a manufacturer and supplier of Budesonide impurities like Budesonide EP impurity A / 16α-Hydroxy prednisolone, Budesonide EP Impurity B, Budesonide EP Impurity C, Budesonide EP Impurity E / Budesonide Related Compound E / 14,15-Dehydro Budesonide, Budesonide EP Impurity F ...
Fawzy Saad Hassan has over 10 years of experience as a consultant for pharmaceutical, biopharmaceutical, and vaccine projects. He has established quality assurance systems, developed validation master plans, conducted technology transfers, and provided GMP training. He is the executive manager of an international consultancy center and has experience working with companies like GSK, Novartis, Sanofi Aventis, and VACSERA.
Yuanzhen Zhong is seeking a new position and has over 25 years of experience in product formulation and development across various industries including pharmaceutical, cosmetic, beverage, and polymer. He has a PhD in Physical Chemistry of Polymers and has held positions at companies like MonoSol Rx, Hartz Mountain, PepsiCo, L'Oreal, and ISP where he successfully developed new products and delivery technologies. He is looking to continue making contributions to new product development.
Founded in 1993, Galenix offers a complete range of services to the pharmaceutical and biotechnology industries. From early stage drug development to the registration, all development processes are performed within our state-of-the-art facilities.. Using a three-stage strategy, Galenix delivers:
-Our innovative Drug Delivery Solutions portfolio offers 6 technologies platforms for oral delivery: Microgix®, Minextab®, Minextab Floating®, Mucolys Film®, Mucolys Flash® and ODTx®.
- The Galenix Drug Product Development process offers customers complete, efficient control over all R&D activities including feasibility studies, API sourcing and characterization, preformulation, formulation, analytical development and validation, Regulatories affairs, consulting and Marketing Authorization Application (MAA) registration. Galenix has obtained more than 50 MAAs over 20 years.
- Galenix licensing-out innovatives Drug Product in OTC and RX Market for Europe, US and others country in the word.
Spécialités : Pharmaceutical Drug Delivery Systems; Drug Product Development and DP Licensing-out
Parveen Bhatarah has over 15 years of experience in pharmaceutical management, API development, drug substance manufacturing, technology transfer, and formulation development. They have successfully developed, scaled up, and manufactured a wide range of drug substances and formulations, and have transferred technologies for commercial manufacturing. Parveen also has experience evaluating and qualifying CMOs, building industry partnerships, and presenting scientific findings to regulatory agencies.
This resume summarizes the career experiences and qualifications of Mizanur Rahman. Over 5 years of experience in production roles at pharmaceutical companies including Mundipharma (Bangladesh) Pvt. Ltd. and Asiatic Laboratory Limited. Extensive skills in pharmaceutical manufacturing processes, quality control, instrumentation, and computer systems. Currently seeking a mid-to-high level position in production, quality assurance, or product development at a pharmaceutical company where he can apply his technical expertise and experience. Well qualified with a Bachelor's degree in Pharmacy.
Lee Anthony Joynston provides a curriculum vitae summarizing his personal details, skills, academic and professional experience. He received a BSc in Biochemistry from the University of Sheffield in 2006, and his third year project involved investigating and purifying the McrC gene product. Since 2013, he has worked as the Production Team Leader at DRFP SmartSeal Ltd, a medical device manufacturing company, where he supervises staff and ensures compliance with quality standards. He has strong communication, organization, and laboratory skills developed through his education and career.
Brian Lam is seeking a position as a QA officer. He has over 2 years of experience working as a QA officer for Bristol Laboratories in the UK where his responsibilities included sampling and testing materials, approving artwork, batch record reviews, audits, and validation activities. He also did a pharmacy clerkship with Watsons Ltd in Hong Kong. Brian has an MSc in Pharmaceutical Technology from the University of Bradford and a BSc in Pharmaceutical Science from the University of Manchester. He has strong technical skills and interpersonal skills.
The document discusses pilot plant scale up techniques for herbal extract formulation production. It defines key terms like pilot plant and scale up. The objectives of pilot plant studies are to produce stable products and identify critical process features. Personnel should have experience in both pilot plant operations and production. A review of the formula, raw materials, and equipment is important. Master manufacturing procedures are developed to guide scale up. Product stability studies ensure uniformity. A case study describes scale up of mangiferin extract from mango leaves from bench to pilot scale.
1. Devendra Singh Rathore is seeking a dynamic career in the pharmaceutical industry utilizing 8 years of experience in production, planning, packaging, and resource management.
2. He has worked as an Executive at Zyg Pharma since 2015 and as a Production Chemist at Osmed Formulation Pvt Ltd from 2012-2015 where he oversaw production and packaging operations.
3. Prior to that he worked as a Chemist at Super Pharma Products from 2008-2011 where he managed batch creation, planning, and packaging operations.
Mohamed Shawky is applying for a QC Manager position and has over 12 years of experience in quality control for pharmaceutical companies. He is currently the QC Manager at Western Pharmaceutical Industries where he manages quality control laboratories and ensures compliance. He has a Bachelor's Degree in Pharmacy and provides his contact information expressing interest in an interview.
The document provides a summary of Ms. Dulari H. Gupta's educational background and work experience in the pharmaceutical regulatory industry. It details her 17+ years of experience in regulatory affairs and quality assurance roles at various pharmaceutical companies. Currently, she works as the Manager of Regulatory Affairs at Glenmark Pharmaceuticals, where she leads the Middle East region and is responsible for regulatory submissions and responding to health authority queries. The document also outlines her responsibilities, achievements, skills, and references.
This document is a resume for Cory M. Zach that outlines his objective, education, and work experience. It summarizes that Zach has over 10 years of experience in quality assurance and regulatory roles within the life sciences industry. He holds an MBA from Webster University and a Bachelor's degree in Biological Sciences. Currently, Zach works as an R&D IT Product Specialist at Monsanto, where he is responsible for rolling out software platforms, collaborating with stakeholders, and identifying opportunities to expand platform usage and grow customers.
Mostafa Mohamed Nassar has over 20 years of experience in pharmaceutical production management, including sterile and non-sterile areas. He is currently the Production Manager at Grand Pharma in Egypt, where he helped start new production lines, develop quality systems, and increase productivity five-fold. Previously, he held production management roles at Adwia and Medical Union Pharmaceutical, where he helped start new sterile facilities and improve quality levels. He has a BSc in Pharmacy from Tanta University and extensive training in sterile manufacturing techniques.
This document contains the curriculum vitae of Mohamed Hosny Abo-samra. It includes his personal details, education history, employment history, training, courses, skills, and personal characteristics. His employment history includes roles as a Quality Control Engineer, Lab Chemist/Supervisor, QC Analytical Chemist, QC Chemist, and Medical Representative. He has a Bachelor's degree in Chemistry and Biochemistry from Alexandria University and specialized training and certifications in quality control, food safety, laboratory analysis, and English.
Tomislav Filipović has over 15 years of experience in laboratory management, sales, and production roles. He has a Bachelor's degree in Food Technology and has worked as a laboratory manager at KONMARKLAB Ltd. where he implemented quality assurance systems and methods validation. He also served as Director, managing business and accounts. Filipović held roles as a laboratory manager and sales representative at LABENA Ltd., and was a production technologist and shift leader at Roto Promet Ltd. His skills include Microsoft Office, English proficiency, and he holds a B category driver's license.
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.
This document discusses pilot plant scale-up techniques for pharmaceutical manufacturing. It defines a pilot plant and scale-up process. The key steps in scale-up involve conducting laboratory and smaller pilot studies, designing and constructing a pilot plant, evaluating results to make corrections, and deciding whether to proceed to full-scale production. General considerations for a pilot plant include personnel requirements, equipment, production rates, process evaluation, and ensuring product stability and uniformity. GMP must also be followed in areas like process validation and documentation.
This document discusses pilot plant scale-up techniques for pharmaceutical manufacturing. It defines a pilot plant and scale-up process. The key steps in scale-up involve conducting laboratory and smaller pilot studies, designing and constructing a pilot plant, evaluating results to make corrections, and deciding whether to proceed to full-scale production. General considerations for a pilot plant include personnel requirements, equipment, production rates, process evaluation, and ensuring product stability and uniformity. GMP must also be followed in areas like process validation and documentation.
This document discusses pilot plant scale-up techniques for pharmaceutical manufacturing. It defines a pilot plant and scale-up process. The key steps in scale-up involve conducting laboratory and smaller pilot studies, designing and constructing a pilot plant, evaluating results to make corrections, and deciding whether to proceed to full-scale production. General considerations for a pilot plant include personnel requirements, equipment, production rates, process evaluation, and ensuring product stability and uniformity. GMP must also be followed in areas like process validation and documentation.
This resume summarizes the educational and professional experience of Mr. Ekkalak Intarapanich. He received a Bachelor's degree in Industrial Chemistry and a Master's degree in Chemical Engineering. He has over 15 years of experience managing projects and production operations in various industries including beverages, plastics, and baby care products. His duties have included project management, production planning, quality control, and facility management. He is proficient in English and seeks a position as a Project Manager.
INDUSTRIAL TRAINING REPORT (B-pharmacy ) Zentiva pharmaceutical industry PrakashKumar721
Location:- GIDC Estate Ankleswar
393002, Dist. Bharuch ,Gujrat India
Zentiva is a producer of high-quality affordable medicines serving patients in Europe and beyond. With a dedicated team of more than 4,700 people and a network of production sites - including flagship sites in Prague, Bucharest and Ankleshwar - Zentiva strives to be the champion of branded and generic medicines in Europe to better supportpeople’s daily healthcare needs. At Zentiva it is our aspiration that healthcare should be a right and not a privilege. More than ever, people need better access to high quality affordable medicines and healthcare. We work in partnership with physicians, pharmacists, wholesalers, regulators and governments to provide the everyday solutions that we all depend on.
About Zentiva’s Ankleshwar site
Established in 1987, the Ankleshwar manufacturing site has a chemistry and biotechnology development center, and manufactures both intermediates and pharmaceutical formulations. A large producer of tablets, the Ankleshwar site manufactures more than 6 billion tablets annually.
Mission &Values:-
Zentiva is a leading developer and supplier of high-quality affordable prescription medicines and consumer brands. As Zentiva grows more people get the medicine they need. Our business is built on trust and responsibility with the patient at the heart of everything we do. Zentiva has established 6 shared SuperpowerZ which frame the values and behaviours we expect of our team and how we will build a healthy business that we can all be proud of.
TABLET-SECTION
Tablet:-
A tablet is a mixture of active substances and excipients, usually in powder form, pressed or compacted into a solid. The excipients include binders, Glidants (flow aids) and lubricants to ensure efficient tabletting, disintegrates to ensure that the tablet breaks up in the digestive tract; sweeteners or flavors to mask the taste of bad-tasting active ingredients; and pigments to make uncoated tablets visually attractive. A coating may be applied to hide the taste of the tablet's components, to make the tablet smoother and easier to swallow, and to make it more resistant to the environment, extending its shelf life.
Advantage
• Production aspect
Large scale production at lowest cost
Easiest and cheapest to package and ship
High stability
• User aspect (doctor, pharmacist, patient)
Easy to handling.
Lightest and most compact.
Greatest dose precision & least content variability.
Coating can mark unpleasant tastes & improve pt. acceptability.
PHARMACEUTICAL PRODUCT BY ZENTIVA PHARMACEUTICAL PVT.LTD:-
1. Avil -25 mg
2. Trental-400
3. Paracetamol-500mg
4. Ramilich-( 5, 25mg)
5. Ramipril-25mg
6. Zuglimate-500mg
7. Clopidogrel-75mg
8. Metformin-100mg
QUALITY CONTROL AND QUALITY ASSUARANCE
Quality control is the part of GMP that deals with sampling, specification, and testing, as well as organisation, documentation, and release procedures to ensure that necessary and
This is an introduction about CCM's experienced projects and products till Feb, 2010, to give you a clear concept about what CCM expertise in and what CCM can help you.
Carmella Moody has over 30 years of experience in regulatory affairs, project management, and quality assurance for pharmaceutical and biotechnology products. She has directed regulatory strategies and submissions to the FDA and international agencies. Her experience includes developing regulatory dossiers, managing clinical trials, gaining regulatory approvals, and developing quality systems. Currently she is the Director of Regulatory Affairs at Pearl Therapeutics, where she is responsible for submissions to approval COPD products.
1. 1/6
SOCIAL REPUBLIC OF VIETNAM
Independence – Freedom – Happiness
CURRICULUM VITAE
PERSONAL DETAILS:
Full Name : Nguyen Trong Tan.
Gender : Male.
Date of Birth : October, 08th
1984.
Marital Status : Married.
Permanent resident : 341/F11 Lac Long Quan, Ward 5, 11 Dist, HCM City, Vietnam.
Hand phone : 0907 290 047
Email : tannt84@gmail.com
Language : Vietnamese (Native), English (Rather)
PERSONAL PROFILE:
+ Character:
Diligent, disciplined and conscientious, self-confident, honest, realistic.
+ Soft Skills:
Independence and decision in working; friendly, collaborative and easily adaptable into new working
environments.
+ Hobby & Passion:
Reading, Pop/Country/Concert music, swimming, ping-pong, football.
EDUCATION PROFILE:
University/Certification Department Degree
Ho Chi Minh City University of Natural Science Chemistry Bachelor
Institute of Science and Technology Catalysis Department Assistant
Education and Development of Chromatography Center Chromatograph Department Assistant
2. 2/6
PRACTICAL EXPERIENCE:
Time Company Description Position
May-2015-
> current
OPV
Pharmaceutical
Co,.Inc
+ Execute project lines and policy of OPV Board of
Director about New Product Development.
+ Improve current formulation quality product, and
make production process more efficient.
+ Research and improve production process for
some dosage form:
- Liquid products (syrup, oral solution):
Lycalci, Opelodil, Acedexphen, etc.
- Semiliquid products: Opeaka cream
- Compressed solid products: Hepeverex,
Askaben 400, Mesalamin 500 EC,etc.
+ Research some medical care products:
- Mouthwash: Fresh gum, Fresh gum 2 in 1.
- Pain gel, Pain cream
+ Provide assistance to Production Head/ Production
Supervisor in resolving technical problems in
operation
R&D
Supervisor.
Responsibility:
o Research new products are suggested and report to Board of Director.
o Scale up to production batch.
o Improve quality of product and manufacturing process.
o Support Registration team to compile pharmaceutical development document (P2) and
manufacturing process for registration and re-registration.
o Advice Board of Director to update R&D machine.
Other Technological Skills:
- Understand in fluently machines using in pharmaceutical field such as: high speed mixer; high speed
granulator; fluid bed dryer; tablet machine; emulsifying machines etc.
3. 3/6
Time Company Description Position
Mar-2012-
> May-
2015
Glomed
Pharmaceutical
Co,.Inc
+ Execute project lines and policy of Board of
Director about New Production.
+ Co-operate and inform project to the concerning
departments preparing (raw material, package,
machine, documents, etc…) for production.
+ Transfer technology and manufacturing process of
new product. Scaling up to production batch.
+ Promote new idea for improvement quantity of
product, efficient production.
+ Transfer successful manufacturing process some
products into production batch:
- Uncompressed solid products (capsule, sachet):
Glucosamin, Eulimen, Optein, etc
- Compressed solid products: Glosicon, Aplorar,
Gliovan-H, Gliovan-HCTZ, Glociten MSM,
Glotadol flu, etc.
+ Improve manufacturing some product:
- Semiliquid products (cream): Glonazol,
Glomazin neo, Glokort, etc.
- Uncompressed solid products (capsule, sachet):
Glucosamin, Glociten , Glothistle, Idium,
Tytdroxil 250, etc
- Compressed solid products: Glotal, Ibumed,
Lodovax, Zadirex, Ranipin, Actixim, etc.
R&D Senior
Specialist.
Responsibility:
o Research new products are suggested and report to R&D Director.
o Execute project lines and policy of Board of Director about new production.
o Improve manufacturing process and control alterations in manufacturing
o Cooperate with QC-RD lab to establish specification of final new product.
4. 4/6
o Support Registration team to compile pharmaceutical development document (P2) and
manufacturing process for registration and re-registration.
o Suggest General Director to buy some machine improving research and production.
Other Technological Skills:
- Understand in fluently machines using in pharmaceutical field such as: high speed mixer; high speed
granulator; fluid bed dryer; tablet machine; film coated machine; Blister packaging machine; Sachet
packing machine; emulsifying machines etc.
Time Company Description Position
Jan-2011-
> Mar-
2012
Glomed
Pharmaceutical
Co,.Inc
+ Ensuring production batches to meet the
requirement of quality and on time of planning.
+ Conduct line audit prior to start of operation as
follows: line purgation, line clearance, line
identification, equipment, materials and document
+ Resolve processing in case of significant deviation
or technical problem and report to Production
Director.
+ Receive transferring and scaling up to production
batch.
+ Review and evaluate batch records accomplished
by Production Operator prior to submission to
Production Director.
+ Planning maintain equipment for production.
+ Perform other duties and responsibility as may be
assigned from time to time.
Production
Supervisor.
Responsibility:
o Cooperate with related departments to planning production batches.
o Manage and supervise manufacturing process.
o Report daily capacity, quality status and arising problem during mass production to Production
Director.
o Contact to maintenance department or outside partners doing maintaining plan.
5. 5/6
Technological skills:
Equipment used for production: high speed mixer; high speed granulator; fluid bed dryer; tablet machine;
film coated machine; Blister packaging machine; Sachet packing machine; emulsifying machines …
Time Company Description Position
Aug-2009-
> Aug-
2010
Glomed
Pharmaceutical
Co,.Inc
+ Research new products are suggested by R&D
Director.
+ Overview the database of new product establishes
formula for lab scale.
+ Monitoring stability testing for lab scale in
accelerated condition, normal conditions reporting to
R&D Director.
+ Send completed formula to Registration team for
Registration.
R&D Staff.
Responsibility:
o Research pharmaceutical products are suggested and report to R&D Director.
o Prepare sample for registration and re-registration (modified formula if any).
o Cooperate with Registration team to compile production document, production validation
document for Registration.
Technological skills:
Equipment used for researching: high speed mixer; high speed granulator; fluid bed dryer; tablet machine;..
Time Company Description Position
Aug-2007
-> Aug-
2009
SPM (Saigon
Pharmaceutics)
Research and application the way of preparing
medicines in manufacture.
R&D Staff
Responsibility:
o Research pharmaceutical products are suggested and report to manager.
o Monitoring of the stability of pharmaceutical products researched.
o To examine the degradation of active ingredient under recommended storage condition & identify
the potential degradation product.
o To innovate manufacturing process.
o Checking before application for manufacture.
o Cooperate with Quality Control Department to compose technical specification of finished product.
o Compile registering medicine documents in Vietnam and overseas.
6. 6/6
Technological skills:
o Equipment used for researching: high speed mixer; high speed granulator; fluid bed dryer; tablet
machine; …
Aug-2008
-> Jan-
2009
SPM (Saigon
Pharmaceutics)
Trained as Quality Control Staff. R&D Staff
Responsibility:
o Learning how to use equipment in Quality Control Department.
o To examine the content of active ingredient in medicine.
o Monitoring of the stability of pharmaceutical products researched.
o To examine the degradation of active ingredient under recommended storage condition.
Technological skill:
o Equipment used for testing: Liquid chromatography machine; UV Spectrophotometer; …
Fer-2007 -
> Jul-2007
Technology
Science Institute
Studying catalysis for hydrogenation of COx
reaction.
Research
Student
Project detail:
o Preparing catalysis for hydrogenation of COx reaction.
o Carry out reaction on those catalysis
o Comparing those catalysis with the catalysis is using in Phu My Manufacture
Responsibility in project:
o Studying catalysis for hydrogenation COx reaction and the way to prepare and report to team
leader.
o Choosing the best catalysis for hydrogenation COx reaction and preparing.
o Designing reaction system to test.
o Testing active and selective catalysis.
o Propose the best catalysis to replace industrial catalysis.
Technologies used in project:
o Equipment used for preparing: Ultrasonic bath; Muffle furnace; …
o Equipment used for testing: Gas chromatography machine.