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To compile, review, and submit dossiers to different Regulatory Bodies (i.e. ASIAN, AFRICAN, ANVISA, LATAM, EU, USother Regulatory as well as non regulated bodies) Needs: knowledge of CTD and ACTD...
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Roles and Responsibilities Job Opening for RA Officer with 1 to 3 Years of Exp in any pharmaceutical company at Ahmedabad. * To prepare & compile registration dossier of ACTD, CTD & R...
bprartcalibrationctddmfcmc regulatory affairsmaaimpdregulatory operationspilcertified meeting professionalpharmaceutical meetingsregulatory intelligencebatch recordsregistrationneesdossier preparationconventionsconference registrationTo compile, review, and submit dossiers to different Regulatory Bodies (i.e. ASIAN, AFRICAN, ANVISA, LATAM, EU, USother Regulatory as well as non regulated bodies) Needs: knowledge of CTD and ACTD...
certified tips trainerlife cyclesample preparationdossier preparationtechnical requirementsprofessional liabilityctdlatamanvisaartworkpackingmarketingregulatorypreparationServSafe InstructionTIPS CertiThe requirement for Assistant Manager QC Analytical Development & Drug Regulatory Affairs for Pharmaceutical Industry Job Responsibility
Roles and Responsibilities Prepare ACTD and CTD regional dossiers Preparation and review of dossiers as per the current prescribe guidelines of respective regulatory authorities. Preparatio...
regulatory affairsanalytical skillspreparationanalyticalregistrationhospitalsregulatorystrong communication skillscommunication skillsfilingenvironmental toxicologyhealthcarecommunicationbiotechnologyctdbasisapicompilationmedicalRoles and Responsibilities Prepare ACTD and CTD regional dossiers Preparation and review of dossiers as per the current prescribe guidelines of respective regulatory authorities. Preparatio...
regulatory affairsanalytical skillspreparationanalyticalregistrationhospitalsregulatorystrong communication skillscommunication skillsfilingenvironmental toxicologyhealthcarecommunicationbiotechnologyctdbasisapicompilationmedicalTo compile, review, and submit dossiers to different Regulatory Bodies (i.e. ASIAN, AFRICAN, ANVISA, LATAM, EU, USother Regulatory as well as non regulated bodies) Needs: knowledge of CTD and ACTD...
certified tips trainerlife cyclesample preparationdossier preparationtechnical requirementsprofessional liabilityctdlatamanvisaartworkpackingmarketingregulatorypreparationServSafe InstructionTIPS CertiGreetings ! We are in Search of Dynamic Individual for Regulatory Affairs activities (Formulations) as detailed below : Company Profile : The multidivisional organi...
regulatory affairsctdproduct registrationformulationinjectableseuropeeuropeandossierfinished dosageactdWith careers in Sales, Marketing, Manufacturing, Research and Development and various other functions we offer a wide range of opportunities. If you would like to be a part of the GUFIC Family, submi...
compilationqualityprotocolsmarketinggmpvalidationwork managementfinished goodsresearch developmentpurchase ordercontinuous improvement facilitationsupply chain managementsupply chainJob Title: Regulatory Affairs (Domestic/ROW/TGA/EU/MHRA & US FDA) Company: Leading Pharma Company in Chennai Location Designation: Assistant Manager to Deputy Manager ...
life cycletech transferregulatory affairsdigital conversiontgausfdapharmaclinicalpipelinebenefitsmanagementhealthcareregulatoryformulationregistrationElectronic Common Technical DocumentfdamedicalTo compile, review, and submit dossiers to different Regulatory Bodies (i.e. ASIAN, AFRICAN, ANVISA, LATAM, EU, USother Regulatory as well as non regulated bodies) Needs: knowledge of CTD and ACTD...
certified tips trainerlife cyclesample preparationdossier preparationtechnical requirementsprofessional liabilityctdlatamanvisaartworkpackingmarketingregulatorypreparationServSafe InstructionTIPS CertiDear Candidate, Greetings of the day! Preparation of CTD as well as ACTD Dossier for ASEAN and African countries as per Guidelines. Registration of pharmaceuticals ...
ctdcompilationregulatory affairs executiveDevelopment Regulatory Documentation, Preparing Dossiers, Review and Filling of Dossiers, Registration in Semi regulated and Regulated Markets and Dossiers preparation for non regulated markets.B.Phar...
regulatory documentationdractdfillingregulatorypreparationregistrationdocumentationpharmaceuticsRegulatory GuidelinesRegulatory IntelligenceDossier PreparationNeeSRegulatory OperationsRegulatory CommunicationsCommon Technical DocumentRegulDevelopment Regulatory Documentation, Preparing Dossiers, Review and Filling of Dossiers, Registration in Semi regulated and Regulated Markets and Dossiers preparation for non regulated markets.B.Phar...
dractdfillingpreparationregistrationdocumentationDossier PreparationNeeSregulaty documentationregulatRegulaty GuidelinesRegulaty IntelligenceRegulaty OperationsRegulaty CommunicationsCommon TechniB.Pharm with diploma/ certificate in DRA M.Pharm(Pharmaceutics) 2 year Experience should be in Development of CTD and ACTD Development Regulatory Documentation,Preparing Dossiers, Review and Filling o...
dractdfillingpreparationregistrationdocumentationDossier PreparationNeeSregulaty documentationregulatRegulaty GuidelinesRegulaty IntelligenceRegulaty OperationsRegulaty CommunicationsCommon TechniExecutive / Sr. Executive - Regulatory Affairs Desired Eligibility Pharma. Graduate and / or Post - Graduate in Science Minimum 2 4 years relevant experience. As per industry norms. Job responsibili...
regulatory affairsctdichscienceregulatorypreparationeligibilityregistrationElectronic Common Technical DocumentRegulatory SubmissionsAbbreviated New Drug ApplicationGeneric ProgrammingCMC Regulatory AffairsComIndian Retail Services requires Out-bound Sales staff ( also called as Feet on Street ) who will go out of the office and meet the customers / merchants at their offices / shops / house. This job will...
Sales Executive Telesales Telecaller Insurance Sales Banking Sales
To compile, review, and submit dossiers to different Regulatory Bodies (i.e. ASIAN, AFRICAN, ANVISA, LATAM, EU, USother Regulatory as well as non regulated bodies) Needs: knowledge of CTD and ACTD...
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Development Regulatory Documentation, Preparing Dossiers, Review and Filling of Dossiers, Registration in Semi regulated and Regulated Markets and Dossiers preparation for non regulated markets.B.Phar...
regulatory documentationdra ctdfilling regulatorypreparation registrationdocumentationDevelopment Regulatory Documentation, Preparing Dossiers, Review and Filling of Dossiers, Registration in Semi regulated and Regulated Markets and Dossiers preparation for non regulated markets.B.Phar...
dra ctd filling preparation registration documentation DossierPreparation NeeS egulat ydocumentation regulat Regulat yGuidelines Regulat yIntelligence Regulat yOperations Regulat yCommunications CommonTechniB.Pharm with diploma/ certificate in DRA M.Pharm(Pharmaceutics) 2 year Experience should be in Development of CTD and ACTD Development Regulatory Documentation,Preparing Dossiers, Review and Filling o...
dra ctd filling preparation registration documentation DossierPreparation NeeS egulat ydocumentation regulat Regulat yGuidelines Regulat yIntelligence Regulat yOperations Regulat yCommunications CommonTechniWith careers in Sales, Marketing, Manufacturing, Research and Development and various other functions we offer a wide range of opportunities. If you would like to be a part of the GUFIC Family, submi...
compilation quality protocols marketing gmp validation orkmanagement finishedgoods researchdevelopment purchaseorder continuousimprovementfacilitation supplychainmanagement supplychain
Development Regulatory Documentation, Preparing Dossiers, Review and Filling of Dossiers, Registration in Semi regulated and Regulated Markets and Dossiers preparation for non regulated markets.B.Phar...
dra ctd filling preparation registration documentation DossierPreparation NeeS egulat ydocumentation regulat Regulat yGuidelines Regulat yIntelligence Regulat yOperations Regulat yCommunications CommonTechniB.Pharm with diploma/ certificate in DRA M.Pharm(Pharmaceutics) 2 year Experience should be in Development of CTD and ACTD Development Regulatory Documentation,Preparing Dossiers, Review and Filling o...
dra ctd filling preparation registration documentation DossierPreparation NeeS egulat ydocumentation regulat Regulat yGuidelines Regulat yIntelligence Regulat yOperations Regulat yCommunications CommonTechniTo compile, review, and submit dossiers to different Regulatory Bodies (i.e. ASIAN, AFRICAN, ANVISA, LATAM, EU, USother Regulatory as well as non regulated bodies) Needs: knowledge of CTD and ACTD...
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Job Location : Mahape, Nearest Station Ghansoli (Navi Mumbai) Look for people from Navi Mumbai or Mumbai Only Only Female Candidates required Qualification : B.Pharm / M.pharm Experience : 1yr 3yr...
clinicalresearch healthcareconsulting research consulting translation egulat yaffairs dossierpreparation ctd pharma salary clinical healthcare regulat preparation registration transp tation MedicalEducation ClinExecutive / Sr. Executive - Regulatory Affairs Desired Eligibility Pharma. Graduate and / or Post - Graduate in Science Minimum 2 4 years relevant experience. As per industry norms. Job responsibili...
regulatory affairsctd ichscience regulatorypreparation eligibilityregistration ElectronJob Location : Mahape, Nearest Station Ghansoli (Navi Mumbai) Look for people from Navi Mumbai or Mumbai Only Only Female Candidates required Qualification : B.Pharm / M.pharm Experience : 1yr 3yr...
clinicalresearch healthcareconsulting research consulting translation egulat yaffairs dossierpreparation ctd pharma salary clinical healthcare regulat preparation registration transp tation MedicalEducation ClinWith careers in Sales, Marketing, Manufacturing, Research and Development and various other functions we offer a wide range of opportunities. If you would like to be a part of the GUFIC Family, submi...
compilation quality protocols marketing gmp validation orkmanagement finishedgoods researchdevelopment purchaseorder continuousimprovementfacilitation supplychainmanagement supplychain
Executive / Senior Executive DRA -ROW Markets
Job Location : Mahape, Nearest Station Ghansoli (Navi Mumbai) Look for people from Navi Mumbai or Mumbai Only Only Female Candidates required Qualification : B.Pharm / M.pharm Experience : 1yr 3yr...
clinicalresearch healthcareconsulting research consulting translation egulat yaffairs dossierpreparation ctd pharma salary clinical healthcare regulat preparation registration transp tation MedicalEducation ClinURGENT REQUIREMENT FOR QUALIFIED AND EXPERIENCED REGULATORY AFFAIRS SPECIALIST FOR FAST GROWING, FINISHED FORMULATIONS CO. QUALIFIED CANDIDATES WITH RELEVANT EXPERIENCE IN REGULATORY AFFAIRS FOR SEMI...
pharma egulatoryaffairsStrong with Regulatory documentation MFR/SOP/AMV(analytical Method Varidation),ACTD/CTD, Dossier Preparation Having a sound knowledge of BMR preparation and filing, FR&D Documentation, PV ETC Will ...
pharmafilingassurancepreparationdocumentationElectronicCommonTechnicalDocumentAbbreviatedNewDrugApplicationGenericProgrammingegulatyaffairsregulatRegulatySubmissions© 2019 Hireejobs All Rights Reserved