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  • B.Sc /M.Sc/ B.Pharma candidate 2-4 years of experience in handling dossiers, CTD, documentation preferably in R&D function

  • 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 ...

  • * 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 ...

  • in the compilation of all trial related documents during the pre-trial period. Follow up with your site team for timely completion of the EDC and will coordinate with delegated site staff to ensure that all the relevant information required in the Case Record Forms are present in the source documents

  • #Initiation and implementation of GMP #To review and approve Standard Operating Procedure (SOP), Batch Manufacturing Record (BMR), Change control, Deviation controls, OOS, OOT investigation & report and distribution of revised documents. #To co-ordinate for technology transfer #To evaluate the reprocessing and reworking procedures #Finished product release record verification #Regulatory document complies ...

  • #Initiation and implementation of GMP #To review and approve Standard Operating Procedure (SOP), Batch Manufacturing Record (BMR), Change control, Deviation controls, OOS, OOT investigation & report and distribution of revised documents. #To co-ordinate for technology transfer #To evaluate the reprocessing and reworking procedures #Finished product release record verification #Regulatory document complies ...

  • #Initiation and implementation of GMP #To review and approve Standard Operating Procedure (SOP), Batch Manufacturing Record (BMR), Change control, Deviation controls, OOS, OOT investigation & report and distribution of revised documents. #To co-ordinate for technology transfer #To evaluate the reprocessing and reworking procedures #Finished product release record verification #Regulatory document complies ...

  • Quality Assurance Management , Analytical Instruments like HPLC ,GC, Spectrophotometer, IC Handling the operations Providing training to all subordinates in cGMP Ensuring the laboratory activities are being carried out as per documented procedures

  • Quality Assurance Management , Analytical Instruments like HPLC ,GC, Spectrophotometer, IC Handling the operations Providing training to all subordinates in cGMP Ensuring the laboratory activities are being carried out as per documented procedures

  • Sort and arrange the pharma requirements received from the hospitals Asking for quotes as per specifications with minimum 3 vendors Negotiation with existing as well as new vendors for better pricing prepare rate comparison and Take aprovals and finalise

  • 1 to 3 years Exp. in Purchase of Hospital Pharmcy Field Visit to Stockist of Pharma Co. Age below 30 years Job Description : Sort and arrange the pharma requirements received from the hospitals Asking for quotes as per specifications with minimum 3 vendors

  • management of Regulatory Affairs, QA & QC functions Monitor regulatory environment and ensure that manufacturing practices comply with the regulatory requirements Ensure strict compliance to cGMP/GLP guidelines in all areas of QC lab Prepare documentation packages for submission to various overseas Please refer the given job description We welcome your prospective applications

  • - Experience Required is 0 to 3 years. - Sampling of sterile raw material related documentation. - Knowledge of Environmental monitoring in aseptic area. - Knowledge of media preparation, media disposal and sterilization. . - Water Sampling analysis. - Candidate should be ready to relocate to Paonta Sahib. -Candidate should have injectable manufacturing experience. -Only Himachali Bonafide candidates will be preferred ...

  • - Experience Required is 0 to 3 years. - Sampling of sterile raw material related documentation. - Knowledge of Environmental monitoring in aseptic area. - Knowledge of media preparation, media disposal and sterilization. . - Water Sampling analysis. - Candidate should be ready to relocate to Paonta Sahib. -Candidate should have injectable manufacturing experience. -Only Himachali Bonafide candidates will be preferred ...

  • agreements Preparation for Board and General meetings. Incorporation of companies under E-Filing system. Filing of Annual Return and Annual Report. Assisted in Preparation of Minutes of the Board Meeting & General Meeting of various Public as well as Private Companies. Inspection of Companys Documents

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