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Vapi

 

Clinical courses

 

Clinical courses

  • One Day National Seminar on Impact of Plagiarism on Research at Academic Level: An Initiative for Plagiarism free India at B.N.B. Swaminarayan Pharmacy College

    ABOUT SMT. B.N.B. SWAMINARAYAN PHARMACY COLLEGE
    To achieve higher learning there is a need of Inspiration. With the divine inspiration and blessings of Lord Swaminarayan and Pujya Swamiji, Smt. B.N.B. Swaminarayan Pharmacy College Salvav Vapi was started in Year 2006 by Shri Swaminarayan Shikshan Seva Kendra trust. Shree Swaminarayan Shikshan seva Kendra trust was established in year 1983 with the noble thought to educate the people of this region. Smt. B.N.B. Swaminarayan Pharmacy College, Salvav, Vapi stands as one of the top Pharmacy college of Gujarat under the pioneering efforts of Pujya KapilJivandas Swamiji and hard-working Team under Principal Dr. Sachin Narkhede, who dreams big and translates it into reality by synthesizing the ideals of our ancient culture with modern technical    education. The institution offers Bachelor of Pharmacy (4 years), Master of Pharmacy (2 years) in specialization subjects like Pharmaceutics and Quality assurance. The college is approved by Pharmacy Council of India (PCI), New Delhi and All India Council for Technical Education (AICTE), New Delhi and affiliated to Gujarat Technological University.

  • REVIEW ON GOOD DOCUMENTATION PRACTICE IN PHARMACEUTICAL MANUFACTURING UNIT AS PER EUROPEAN UNION GMP CHAPTER-4 ON DOCUMENTATION

    { DOWNLOAD AS PDF }

    ABOUT AUTHORS
    Suleman S. khoja * 1, Dr. L J. Patel 2, Sohil S. Khoja 3, Karim R. Panjwani 3, Jagdish Ray3
    1 PhD. Research Scholar, Ganpat University, Mehesana, Gujarat, India
    2 Faculty of Pharmacy, Ganpat University, Mehesana, Gujarat, India
    3 Resource person, Pharmaceutical Quality Assurance, Audit and Compliance, Vapi, Gujarat, India

    ABSTRACT
    Good documentation constitutes an essential part of the quality assurance system and is key to operating in compliance with GMP requirements. Documentation requirements of maintaining complete, accurate, truthful and verifiable data in all cGXP documents that are needed to be maintained as per regulatory requirements and various Governmental regulations, laws, rules and statutes/acts. Documentation may exist in a variety of forms, including paper-based, electronic or photographic media. Ensure that the Document should be free from error and during any point if error identify then rectify with proper reason for correcting including sign and date. A system should be in place to indicate special observations and any changes to critical data. GMP Document must have predefined retention period and document must be stored in secure and easy to retrieve or easily available as and when required. Batch Processing and Packaging Instruction must be in place and Contemporaneous entry provision must be available. Instruction and procedure for using equipment; instrument must be clear and specific.  Specification with authorization should be available for analysis of Raw Material and Packing Material, Intermediate and Bulk Product, Finished Product.

  • Walk in interview for M.Pharm, B.Pharm, M.Sc in Quality Control, Quality Assurance at Glenmark Pharmaceuticals

    Glenmark Pharmaceuticals Ltd is one of India's leading research-driven, global, integrated pharmaceutical company. Glenmark has Offices in over 40 Countries. It has 17 manufacturing facilities in 5 countries, with over 12.000 employees from over 60 nationalities. 5 world-class research and development center, the group is dedicated to improving people live. We have following vacancies at our API Manufacturing location at Ankleshwar, Gujarat.

  • Walk in interview for M.Pharm, B.Pharm, M.Sc in Production, Packing, QC, QA at Alembic Limited

    Alembic Limited, with an established presence in the Indian pharma  industry has a proud, historical track record going back one hundred years. With a turnover in excess of Rs1000 crores today, Alembic Limited is one of India’s leading integrated pharmaceutical companies. We continue to enjoy leadership positions in antibiotics, anti-infective, anti-cough and also have significant worldwide presence in specialty therapeutic areas such as cardiology, neurology, diabetology, etc. We have also plans for expansion in Ophthalmic etc.

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  • Job in Quality Assurance, Quality Control, Production at UMEDICA | M.Pharm, B.Pharm, M.Sc

    UMEDICA is a part of the Amoli Group of Companies, manufacturing and exporting a wide range of formulations viz; Injectable, Tablets, Capsules, Suspensions, Dry Syrups, etc. UMEDICA offers a diverse product portfolio comprising of antibiotics, non-steroidal anti-inflammatory (NSAIDs), analgesics, antifungal, antiviral, anti-malarial, anti-tuberculosis agents, antihistaminic, psychotropic, anti-hypertensive, lipid lowering agents, drugs for sexual dysfunction, multivitamins etc.

  • Job in Quality Assurance, Quality Control, Production, ADL, F&D at Aculife Healthcare | M.Pharm, B.Pharm, M.Sc

    Aculife Healthcare Private Limited is one of world’s largest Infusion & Injectable Company, having its global operation spread across 70 countries including JV Company in Brazil & wholly owned subsidiary in Mexico. 8 Manufacturing Plants Backed up by state of the art. Aculife Research Centre & 4000 plus Employee base in India & abroad. To keep up with the scale of operations & requirements of regulated and semi regulated markets, Aculife is enhancing its focus on healthcare initiatives across the global Markets.

  • Walk in interview for B.Pharm, B.Sc in Quality Control, Quality Assurance, Production, Packaging Development at Mylan Laboratories

    Mylan is one of the world's leading generic and speciality pharmaceutical company, providing products in around, 150 countries, through our global workforce of more than 18,000 passionate leaders. If you resonate with our audacious ambition to provide the world's 7 billion population with access to high quality medicine, with state of art og finished dosage form manufacturing facility at Aurangabad. These facilities are compliant of USFDA, WHO, MHRA & MCC.

  • Walk in interview for M.Pharm, B.Pharm, M.Sc in Production, Packing, Quality Control at Alembic Limited

    Alembic LimitedAlembic Limited, with an established presence in the Indian pharma  industry has a proud, historical track record going back one hundred years. With a turnover in excess of Rs1000 crores today, Alembic Limited is one of India’s leading integrated pharmaceutical companies. We continue to enjoy leadership positions in antibiotics, anti-infective, anti-cough and also have significant worldwide presence in specialty therapeutic areas such as cardiology, neurology, diabetology, etc. We have also plans for expansion in Ophthalmic etc.

  • Walk in interview for M.Pharm, M.Sc in Quality Control, Quality Assurance at Macleods

    Macleods has its presence in over 30 countries with more than 300 registrations.The export range of Macleods are manufactured in a unit that has QSM approval from WHO-Geneva, and certifications from various International Regulatory Authorities like - USFDA, MCC, UKMHRA, MOH – Belarus, INVIMA – Colombia, National Drugs Authority - Uganda, Food and Drugs Board - Ghana, MCAZ – Zimbabwe, Pharmacy and Poisons Board Kenya, Pharmacy Board Tanzania etc.

  • Walk in Interview for M.Pharm, B.Pharm, M.Sc in Quality Control at Ajanta Pharma Limited

    Ajanta Pharma Limited is a specialty pharmaceutical company engaged in development, manufacture and marketing of quality finished dosages in domestic and international markets. We are looking suitable candidates for below openings at our flagship formulation facility located at Paithan Aurangabad, which is approved by the US FDA, UK MHRA. It also holds WHO pre- qualification.

    Post : QC Sr. executive/Executive/Sr. Officer / Officer

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