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23 jobs found for Qa Validation Pharma Gmp Manager

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  • Experience in QA in Pharma Industry. Well-versed with & effective to maintain the reqd GMP norms & QMS in Export oriented unit as a whole. Experience to face the regulatory audits in front line.(SEA, Africa, CIS, GCC etc) Familiar with domestic regulatory procedures & liaison with FDA & CDSCO. Hands-on experience in validations, qualifications & related GMP documentations. FDA approved in QC for batch release ...

  • * Prepare production plan as per requirement * Overall Production department activity * GMP Documentation * Make, Review, Verify SOPs & Train team as per CGMP norms * Online Completion and Reviewing of BMR/BPR * Co-ordinate with all department * Manpower management * participate with CVG/QA during validation of area * Evaluation and investigation of all market complaints and necessary corrective and preventive ...

  • * Prepare production plan as per requirement * Overall Production department activity * GMP Documentation * Make, Review, Verify SOPs & Train team as per CGMP norms * Online Completion and Reviewing of BMR/BPR * Co-ordinate with all department * Manpower management * participate with CVG/QA during validation of area * Evaluation and investigation of all market complaints and necessary corrective and preventive ...

  • * Prepare production plan as per requirement * Overall Production department activity * GMP Documentation * Make, Review, Verify SOPs & Train team as per CGMP norms * Online Completion and Reviewing of BMR/BPR * Co-ordinate with all department * Manpower management * participate with CVG/QA during validation of area * Evaluation and investigation of all market complaints and necessary corrective and preventive ...

  • Experience in QA in Pharma Industry. Well-versed with & effective to maintain the reqd GMP norms & QMS in Export oriented unit as a whole. Experience to face the regulatory audits in front line.(SEA, Africa, CIS, GCC etc ...

  • Experience in QA in Pharma Industry. Well-versed with & effective to maintain the reqd GMP norms & QMS in Export oriented unit as a whole. Experience to face the regulatory audits in front line.(SEA, Africa, CIS, GCC etc ...

  • Experience in QA in Pharma Industry. Well-versed with & effective to maintain the reqd GMP norms & QMS in Export oriented unit as a whole. Experience to face the regulatory audits in front line.(SEA, Africa, CIS, GCC etc ...

  • ANALYTICAL R&D, METHODS, VALIDATIONS, QC KNOWLEDGE, CALIBRATION, FORMULATION DEVELOPMENT, GMP/GLP, SOP/ STP, DOCUMENTATION, TROUBLESHOOTING GC, HPLC. ANALYTICAL R&D IN FORMULATION, KNOWLEDGE OF ICH GUIDELINES, CONDUCT MULTIMEDIA DISSOLUTION, ANALYSIS OF THE DEVELOPMENTAL SAMPLES AND STABILITY SAMPLES AT EACH STAGE OF FORMULATIONS DEVELOPMENT, FOLLW GLP, SOP & STP ...

  • and providing inputs to concerned to schedule. Responsible for review of URS/DQ/IQ/OQ/PQ of new equipment, instruments facility, utility and systems and providing inputs to concerned to schedule. Make proposals and implement actions as part of the continuous improvement program to improve validation policies Should have exposure of regulatory audits e.g. USFDA, MHRA, EDQM etc. Should have experience in ...

  • control, deviations, market complaint handling, product recall, product return, failure investigations & root cause analysis o Facilitation and closure of the CAPA's resulting from audits, investigations, failures, complaints and/or recalls o Maintenance of CGMP Managing GMP / GLP Quality Assurance

  • control, deviations, market complaint handling, product recall, product return, failure investigations & root cause analysis o Facilitation and closure of the CAPA's resulting from audits, investigations, failures, complaints and/or recalls o Maintenance of CGMP Managing GMP / GLP Quality Assurance

  • control, deviations, market complaint handling, product recall, product return, failure investigations & root cause analysis o Facilitation and closure of the CAPA's resulting from audits, investigations, failures, complaints and/or recalls o Maintenance of CGMP Managing GMP / GLP Quality Assurance

  • control, deviations, market complaint handling, product recall, product return, failure investigations & root cause analysis o Facilitation and closure of the CAPA's resulting from audits, investigations, failures, complaints and/or recalls o Maintenance of CGMP Managing GMP / GLP Quality Assurance

  • control, deviations, market complaint handling, product recall, product return, failure investigations & root cause analysis o Facilitation and closure of the CAPA's resulting from audits, investigations, failures, complaints and/or recalls o Maintenance of CGMP Managing GMP / GLP Quality Assurance

  • control, deviations, market complaint handling, product recall, product return, failure investigations & root cause analysis o Facilitation and closure of the CAPA's resulting from audits, investigations, failures, complaints and/or recalls o Maintenance of CGMP Managing GMP / GLP Quality Assurance

  • To lead a team for Qualifications, in-process and Quality management system for effective implementation of Quality Assurance across the sterile Solid Oral Dosage plant. Handling of internal, customer, international and regulatory audits and successful compliance. Management of new projects

  • Urgently required QA - Microbiologist for a Chemical Company (FREE JOBS) Post: QA- Microbiologist Location Gangtok, East Sikkim Experience: 2 - 5 yrs. Job Description: 1. Quality control of all incoming raw materials, water, WIP and finished product for Micro evaluation. 2. Equipment monitoring

  • Handling O&M of Electro-Mechanical setup, HVAC (High & Low Side), Utilities & Water Generation / Distribution system. Exercising Power Trading. Qualification & Validation of Labs / HVAC setup. Compliance with cGMP/GLP norms. Ensuring smooth distribution of power and other utilities to all the R&D facilities including exercising open access power trading on routine basis. O&M of Chillers, BMS, Condenser ...

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