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601 jobs found for Bank Assurance Delhi

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  • and development needs Knowledge of and understanding of processes, tools and techniques for assuring high level of quality of technology products, systems and components. Knowledge of major functional processes and associated operating requirements; ability to apply this knowledge appropriately to diverse

  • Opening for quality assurance with exp in tablets , syrups , capsules in formulation etc

  • of an Associates Degree in Chemistry or related field. 4+ years lab experience. Planning and organizational skills. Quality Assurance experience preferred ...

  • requirements. Quality monitoring on machines as well as finishing for the compliance audit. Co-ordination with Q.C inspection of buying house to get the inspection done at the time of Fittings , Initials, Inline, Midline & Final. To make assurance that the all quality standards are followed on the production

  • requirements. Quality monitoring on machines as well as finishing for the compliance audit. Co-ordination with Q.C inspection of buying house to get the inspection done at the time of Fittings , Initials, Inline, Midline & Final. To make assurance that the all quality standards are followed on the production

  • requirements. Quality monitoring on machines as well as finishing for the compliance audit. Co-ordination with Q.C inspection of buying house to get the inspection done at the time of Fittings , Initials, Inline, Midline & Final. To make assurance that the all quality standards are followed on the production

  • Purpose of the Position Head- QA: The Profile requires the person to handle all QA activities and to ensure that QMS is effectively implemented as per ISO 9001:2008 & current GMP guidelines. Job Responsibility: 1. Responsible for review and approval of all SOPs, protocols and master controlled documents. 2. Responsible for review and approval of all OOS, Deviation, Change Control, Market Complaint and product ...

  • Experience in the field of quality- inspection, test and monitoring Preparing rejection analysis, charts and R& D. 3-4 years experience in the field of quality- inspection, test, monitoring Preparing rejection analysis, charts and R& D. Location - Noida

  • Purpose of the Position (Incharge- CQA): The Profile requires the person to handle CQA activities and to ensure that all CQA guidelines are prepared based on current GMP and ISO guidelines. 1. Responsible for preparation, review and approval of guidelines to prepare QMS documents as per ISO and GMP guidelines. 2. Responsible to conduct trainings on QMS guidelines as per ISO and GMP requirements. 3. To give ...

  • 1- To perform and monitor document and data control of all controlled documents (Issuance, retrieval, archival and distribution). 2- To update all master documents periodically. 3- To ensure that APQRs are prepared, reviewed and approved as per approved procedure 4- To prepare & review of all SOPs, protocols and master controlled documents. 5- To do documentation related to OOS, Non conformity, Deviation, CAPA ...

  • Purpose of the Position Head- QA: The Profile requires the person to handle all QA activities and to ensure that QMS is effectively implemented as per ISO 9001:2008 & current GMP guidelines. Job Responsibility: 1. Responsible for review and approval of all SOPs, protocols and master controlled documents. 2. Responsible for review and approval of all OOS, Deviation, Change Control, Market Complaint and product ...

  • 1. Responsible for review and approval of all SOPs, protocols and master controlled documents. 2. Responsible for review and approval of all OOS, Deviation, Change Control, Market Complaint and product recall. 3. To represent company during external/regulatory audits. 4. Responsible for conducting self-inspection/ internal audit as per schedule. 5. To impart trainings on QMS, ISO and cGMP guidelines. 6. To ...

  • 1- To perform and monitor document and data control of all controlled documents (Issuance, retrieval, archival and distribution). 2- To update all master documents periodically. 3- To ensure that APQRs are prepared, reviewed and approved as per approved procedure 4- To prepare & review of all SOPs, protocols and master controlled documents. 5- To do documentation related to OOS, Non conformity, Deviation, CAPA ...

  • Purpose of the Position Head- QA: The Profile requires the person to handle all QA activities and to ensure that QMS is effectively implemented as per ISO 9001:2008 & current GMP guidelines. Job Responsibility: 1. Responsible for review and approval of all SOPs, protocols and master controlled documents. 2. Responsible for review and approval of all OOS, Deviation, Change Control, Market Complaint and product ...

  • Purpose of the Position Head- QA: The Profile requires the person to handle all QA activities and to ensure that QMS is effectively implemented as per ISO 9001:2008 & current GMP guidelines. Job Responsibility: 1. Responsible for review and approval of all SOPs, protocols and master controlled documents. 2. Responsible for review and approval of all OOS, Deviation, Change Control, Market Complaint and product ...

  • To carry out all kind of controls/inspections like PPM, Inline, Mid, Final audits etc. as per AQL system & as defined by the buyer in order to get product in right desired quality within the given delivery date To ensure that the quality SOPs

  • Purpose of the Position (Incharge- CQA): The Profile requires the person to handle CQA activities and to ensure that all CQA guidelines are prepared based on current GMP and ISO guidelines. 1. Responsible for preparation, review and approval of guidelines to prepare QMS documents as per ISO and GMP guidelines. 2. Responsible to conduct trainings on QMS guidelines as per ISO and GMP requirements. 3. To give ...

  • 1- To perform and monitor document and data control of all controlled documents (Issuance, retrieval, archival and distribution). 2- To update all master documents periodically. 3- To ensure that APQRs are prepared, reviewed and approved as per approved procedure 4- To prepare & review of all SOPs, protocols and master controlled documents. 5- To do documentation related to OOS, Non conformity, Deviation, CAPA ...

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