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16 jobs found for Pharma Regulatory Affairs Mumbai Executive

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  • 1 -3 years' work experience in international regulatory affairs from Pharma industry and Confirmed knowledge of EU requirements and ICH guidelines. Knowledge of Regulatory requirements as per UKMHRA, MCC, TGA, USFDA, ANVISA ACTD guidelines ...

  • 1 -3 years' work experience in international regulatory affairs from Pharma industry and Confirmed knowledge of EU requirements and ICH guidelines. Knowledge of Regulatory requirements as per UKMHRA, MCC, TGA, USFDA, ANVISA ACTD guidelines ...

  • 2 -5 years' work experience in international regulatory affairs from Pharma industry and Confirmed knowledge of EU requirements and ICH guidelines. Knowledge of Regulatory requirements as per UKMHRA, MCC, TGA, USFDA, ANVISA ACTD guidelines ...

  • 1 -3 years' work experience in international regulatory affairs from Pharma industry and Confirmed knowledge of EU requirements and ICH guidelines. Knowledge of Regulatory requirements as per UKMHRA, MCC, TGA, USFDA, ANVISA ACTD guidelines ...

  • 1 -3 years' work experience in international regulatory affairs from Pharma industry and Confirmed knowledge of EU requirements and ICH guidelines. Knowledge of Regulatory requirements as per UKMHRA, MCC, TGA, USFDA, ANVISA ACTD guidelines ...

  • 1. Executive / Sr Officer / officer - Regulatory Affairs 2. Location: Mumbai 3) Experience: 2years to 5years 4) Education: B Pharm/ M Pharm/ MSC/ BSC 5) Gender: Male / Female 6) CTC: 2.00L to 6.00L 6) J D : Experience in preparing dosseirs for ROW market ...

  • Qualification: B Pharm/M Pharma. 4-8 years experience. Should have hands on experience for ANDA preparations & submissions. Knowledge of ICH / FDA Guidance documents. OCR, Book marking, hyperlinking, QC check. Coordinating and collating the documents relevant to ANDA compilation from different functions. Review of documents for adequacy (wrt content, requirements, legibility, PDF requirements, et ...

  • 1 -3 years' work experience in international regulatory affairs from Pharma industry and Confirmed knowledge of EU requirements and ICH guidelines. Knowledge of Regulatory requirements as per UKMHRA, MCC, TGA, USFDA, ANVISA ACTD guidelines ...

  • 1 -3 years' work experience in international regulatory affairs from Pharma industry and Confirmed knowledge of EU requirements and ICH guidelines. Knowledge of Regulatory requirements as per UKMHRA, MCC, TGA, USFDA, ANVISA ACTD guidelines ...

  • 2 -5 years' work experience in international regulatory affairs from Pharma industry and Confirmed knowledge of EU requirements and ICH guidelines. Knowledge of Regulatory requirements as per UKMHRA, MCC, TGA, USFDA, ANVISA ACTD guidelines ...

  • -Overall responsibility of DRA-ROW. -Planning and executing of dossiers as per the schedule finalized with marketing -Timely dispatches of queries (within 15days from the day of receipt) -Co-ordination with Marketing / Commercial/ PPIC / other departments within Advent for matters related

  • Exposure in OOS,OOT investigation,Vendor qualification,vendor Audit,CTD,DMF,Root Cause Analysis,CAPA,Change controls,Market Complaints,Preparation and review of Annual product quality review document,Validation & qualification,regulatory affairs ...

  • Exposure in OOS,OOT investigation,Vendor qualification,vendor Audit,CTD,DMF,Root Cause Analysis,CAPA,Change controls,Market Complaints,Preparation and review of Annual product quality review document,Validation & qualification,regulatory affairs ...

  • Exposure in OOS,OOT investigation,Vendor qualification,vendor Audit,CTD,DMF,Root Cause Analysis,CAPA,Change controls,Market Complaints,Preparation and review of Annual product quality review document,Validation & qualification,regulatory affairs,Aud

  • 1. Executive / Sr Officer / officer - QC 2. Location: Mumbai 3) Experience: 2years to 5years 4) Education: MSC/ BSC 5) Gender: Male 6) J D : should have knowledge of Co-ordination with concern department to Q.A. / Production / Stores& regulatory . Experieince into Instrumentation and analysis

  • Obtaining approval of shareholders on all proposals at the Annual General Meeting. Updating of websites Close on all Action items arising out of Board and committee meetings and systematic reporting of the same. Liasioning with various Regulatory authorities / external agencies on behalf Have Past Working Experience in Similar roles. Able to Handle all compliance work ...

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