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Designation: Senior Executive Job Location: Bangalore Department: Quality Assurance - GLP About Syngene Incorpo...
audit trailcustomer relationscontinuous improvement facilitationsalesdeliverymismethod developmentcustomer serviceequal employment opportunityanimal health21 cfrconsumer goodscommitment towards workDesignation: Senior Executive Job Location: Bangalore Department: Quality Assurance - GLP About Syngene Incorpo...
audit trailcustomer relationscontinuous improvement facilitationsalesdeliverymismethod developmentcustomer serviceequal employment opportunityanimal health21 cfrconsumer goodscommitment towards workDesignation: Senior Executive Job Location: Bangalore Department: Quality Assurance - GLP About Syngene Incorpo...
audit trailcustomer relationscontinuous improvement facilitationsalesdeliverymismethod developmentcustomer serviceequal employment opportunityanimal health21 cfrconsumer goodscommitment towards workDesignation: Senior Executive Job Location: Bangalore Department: Quality Assurance - GLP About Syngene Incorpo...
audit trailcustomer relationscontinuous improvement facilitationsalesdeliverymismethod developmentcustomer serviceequal employment opportunityanimal health21 cfrconsumer goodscommitment towards workDesignation: Senior Executive Job Location: Bangalore Department: Quality Assurance - GLP About Syngene Incorpo...
audit trailcustomer relationscontinuous improvement facilitationsalesdeliverymismethod developmentcustomer serviceequal employment opportunityanimal health21 cfrconsumer goodscommitment towards workDesignation: Senior Executive Job Location: Bangalore Department: Quality Assurance - GLP About Syngene Incorpo...
audit trailcustomer relationscontinuous improvement facilitationsalesdeliverymismethod developmentcustomer serviceequal employment opportunityanimal health21 cfrconsumer goodscommitment towards workDesignation: Senior Executive Job Location: Bangalore Department: Quality Assurance - GLP About Syngene Incorpo...
audit trailcustomer relationscontinuous improvement facilitationsalesdeliverymismethod developmentcustomer serviceequal employment opportunityanimal health21 cfrconsumer goodscommitment towards workDesignation: Senior Executive Job Location: Bangalore Department: Quality Assurance - GLP About Syngene Incorpo...
audit trailcustomer relationscontinuous improvement facilitationsalesdeliverymismethod developmentcustomer serviceequal employment opportunityanimal health21 cfrconsumer goodscommitment towards workDesignation: Senior Executive Job Location: Bangalore Department: Quality Assurance - GLP About Syngene Incorpo...
audit trailcustomer relationscontinuous improvement facilitationsalesdeliverymismethod developmentcustomer serviceequal employment opportunityanimal health21 cfrconsumer goodscommitment towards workDesignation: Senior Executive Job Location: Bangalore Department: Quality Assurance - GLP About Syngene Incorpo...
audit trailcustomer relationscontinuous improvement facilitationsalesdeliverymismethod developmentcustomer serviceequal employment opportunityanimal health21 cfrconsumer goodscommitment towards workDesignation: Senior Executive Job Location: Bangalore Department: Quality Assurance - GLP About Syngene Incorpo...
audit trailcustomer relationscontinuous improvement facilitationsalesdeliverymismethod developmentcustomer serviceequal employment opportunityanimal health21 cfrconsumer goodscommitment towards workDesignation: Senior Executive Job Location: Bangalore Department: Quality Assurance - GLP About Syngene Incorpo...
audit trailcustomer relationscontinuous improvement facilitationsalesdeliverymismethod developmentcustomer serviceequal employment opportunityanimal health21 cfrconsumer goodscommitment towards workDesignation: Senior Executive Job Location: Bangalore Department: Quality Assurance - GLP About Syngene Incorpo...
audit trailcustomer relationscontinuous improvement facilitationsalesdeliverymismethod developmentcustomer serviceequal employment opportunityanimal health21 cfrconsumer goodscommitment towards workTo 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 CertiEY- GDS Consulting Enterprise Risk (ER) Regulatory Compliance Senior As part of our EY-ER- Regulatory Compliance team, you will help the clients by understanding their business need...
software quality assuranceit risk21 cfrlife cycleenvironmental impact assessmentclient focuscomputer system validationfortune 500test scriptsbusiness process transformationstatements of work sowEY- GDS Consulting Enterprise Risk (ER) Regulatory Compliance Senior As part of our EY-ER- Regulatory Compliance team, you will help the clients by understanding their business need...
it risk21 cfrlife cycleenvironmental impact assessmentclient focuscomputer system validationfortune 500test scriptssoftware quality assurancebusiness process transformationQUALITY MANAGEMENT SYSTEM:
The opportunity We re looking for Senior Manager with expertise in Life Sciences Regulatory Compliance and Stakeholder Management to join the leadership group of our EY-Regulatory Compl...
financecomplianceadvisory21 cfrcustomer relationsfortune 500life cyclereportingcertified software quality engineersoftware quality assurancebusiness process transformationstatements of work sowEY- GDS Consulting Enterprise Risk (ER) Regulatory Compliance Senior As part of our EY-ER- Regulatory Compliance team, you will help the clients by understanding their business ...
software quality assurancelife cycletest scriptsclient focusquality auditrisk analysisservice linesdata integrityquality systemquality controlrisk managementrisk assessmentPosition Description- Product Support Specialist/Business AnalystRole Description Responsible for a specific area of the system for one or more markets, understandin...
business rulesproduct supportsystem analysisimpact analysischange requestsuser requirementshealth informaticsorganization skillsinformation securitywritten communicationemerging technologiesSALARY: 7-8 LPA LOCATION : Mumbai, Maharashtra, INDIA VACANCIES: 1 QUALIFICATION: At least a Bachelor s Degree in Science MALE/FEMALE:...
isoquality controlsafetyqualitybudgetingcontinuous improvement facilitationman powerrisk assessmentpower managementquality assuranceregulatory auditsmanpower managementLocation:Bengaluru Area, India Qualification: B. Pharma / M. Pharmacy / M.Sc., 2 - 10 years of Experience in BA BE centre (CRO)/ pharma is preferred. 1. To oversee that the quality system is establis...
isofeasibility studiesgraphic designhydraulicsnew product developmentmusic makinginternal auditquality systemquality controlquality managementcase rept fstudy reprective actionsinternationCapabilities: Thorough understanding and on-hand experience in Analytical Method Development, Validation and Stability Studies as per EU/US requirements. Having thorough knowledge of impurity profilin...
method developmentanalytical method developmentJob Description and responsibilities; - Capabilities: In- depth understanding of GMPs, US FDA, MHRA UK, EU, ANVISA Brazil, TGA Australia, MCC South Africa, ICH Regulatory guidelines. Should have exp...
analytical researchcontinuous improvement facilitationJob Description and responsibilities; - Capabilities: Thorough understanding and on- hand experience in Analytical Method Development, Validation and Stability Studies as per EU/ US requirements. Ha...
documentationresearchanalytical method developmentmethod developmentThorough understanding and on- hand experience in Analytical Method Development, Validation and Stability Studies as per EU/ US requirements. Having thorough knowledge of impurity profiling, dissoluti...
operationsmethod developmentregulatory auditsanalytical method developmentCapabilities: Thorough understanding and on- hand experience in Analytical Method Development, Validation and Stability Studies as per EU/ US requirements. Having thorough knowledge of impurity profil...
analytical method developmentregulatorymhraftirusfdatgainstrumentsanvisadissolutionmccvalidationstability studieshplcregulatory auditsanalyticalmethod developmentvariance analysisoperationsfdaCapabilities: In- depth understanding of GMPs, US FDA, MHRA UK, EU, ANVISA Brazil, TGA Australia, MCC South Africa, ICH Regulatory guidelines. Should have experience in ANDA/ DMF filing for advanced m...
analyticalkaizenregulatoryresearchfilingroot cause analysisanalytical researchcontinuous improvement facilitationpharma researchcontinuous improvement cultureJob Title: Quality Assurance (QA) Head Company: Leading Pharma API Bulk drug Company in Vizag Location Designation: GM & Above Reporting to: CEO...
quality controlmusic makingshop floorpurified watercustomer auditsinspectioncomplianceregulatory auditsisomanagement systemauditingquality managementcontinuous improvement facilitationquality management systemraw materialsprocess validationEY- GDS Consulting Enterprise Risk (ER) Regulatory Compliance Senior As part of our EY-ER- Regulatory Compliance team, you will help the clients by understanding their business ...
software quality assurancecomputer system validationenvironmental impact assessmentbusiness process transformationtest scriptsTo 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 CertiQualifications: M. Sc. /5M. Pharm/5Ph. D. Capabilities: Thorough understanding and on-hand experience in Analytical Method Development, Validation and Stability Studies as per EU...
analytical method developmentmethod developmentCapabilities: In- depth understanding of GMPs, US FDA, MHRA UK, EU, ANVISA Brazil, TGA Australia, MCC South Africa, ICH Regulatory guidelines. Should have experience in ANDA/ DMF filing for advanced m...
analyticalkaizenregulatoryresearchfilingroot cause analysisanalytical researchcontinuous improvement facilitationpharma researchcontinuous improvement cultureJob Description and responsibilities; - Capabilities: Thorough understanding and on- hand experience in Analytical Method Development, Validation and Stability Studies as per EU/ US requirements. Ha...
documentationresearchanalytical method developmentmethod developmentCapabilities: Thorough understanding and on-hand experience in Analytical Method Development, Validation and Stability Studies as per EU/US requirements. Having thorough knowledge of impurity profilin...
method developmentanalytical method developmentJob Description and responsibilities; - Capabilities: In- depth understanding of GMPs, US FDA, MHRA UK, EU, ANVISA Brazil, TGA Australia, MCC South Africa, ICH Regulatory guidelines. Should have exp...
analytical researchcontinuous improvement facilitationThorough understanding and on- hand experience in Analytical Method Development, Validation and Stability Studies as per EU/ US requirements. Having thorough knowledge of impurity profiling, dissoluti...
operationsmethod developmentregulatory auditsanalytical method developmentCapabilities: Thorough understanding and on- hand experience in Analytical Method Development, Validation and Stability Studies as per EU/ US requirements. Having thorough knowledge of impurity profil...
analytical method developmentregulatorymhraftirusfdatgainstrumentsanvisadissolutionmccvalidationstability studieshplcregulatory auditsanalyticalmethod developmentvariance analysisoperationsfdaLocation:Bengaluru Area, India Qualification: B. Pharma / M. Pharmacy / M.Sc., 2 - 10 years of Experience in BA BE centre (CRO)/ pharma is preferred. 1. To oversee that the quality system is establis...
isofeasibility studiesgraphic designhydraulicsnew product developmentmusic makinginternal auditquality systemquality controlquality managementcase rept fstudy reprective actionsinternationSound knowledge of about semi regulated and regulated markets like USFDA, EU, MHRA, TGA, ANVISA, Canadian market. Knowledge of addressing regulatory deficiencies. Exposure to regulatory audits. Review...
tgamhrasoundusfdaanvisafillingpreparationEuropean PoliticsEuropean IntegrationEuropean StudiesEuropean AffairsEU FundingEuropean Union PoliticsInternational OrganizationsDemocracyregulatTransatlanKnowledge of about Preparation of Dossier. Sound knowledge of about semi regulated and regulated markets like USFDA, EU, MHRA, TGA, ANVISA, Canadian market. Knowledge of addressing regulatory deficien...
tgamhrasoundusfdaanvisafillingpreparationEuropean PoliticsEuropean IntegrationEuropean StudiesEuropean AffairsEU FundingEuropean Union PoliticsInternational OrganizationsDemocracyregulatTransatlanTo 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...
certifiedtipstrainer lifecycle samplepreparation dossierpreparation technicalrequirements professionalliability eu ctd latam anvisa artwork packing marketing regulatory preparation ServSafeInstruction IPSCertiKnowledge of about Preparation of Dossier. Sound knowledge of about semi regulated and regulated markets like USFDA, EU, MHRA, TGA, ANVISA, Canadian market. Knowledge of addressing regulatory deficien...
tga mhra sound usfda anvisa filling preparation EuropeanPolitics EuropeanIntegration EuropeanStudies EuropeanAffairs EUFunding EuropeanUnionPolitics InternationalOrganizations Democracy egulat TransatlanQualifications: M. Sc. /5M. Pharm/5Ph. D. Capabilities: Thorough understanding and on-hand experience in Analytical Method Development, Validation and Stability Studies as per EU/US requirements. Ha...
nalytical method development method developmentCapabilities: Thorough understanding and on- hand experience in Analytical Method Development, Validation and Stability Studies as per EU/ US requirements. Having thorough knowledge of impurity profil...
analyticalmethoddevelopment regulatory mhra ftir usfda tga instruments anvisa dissolution mcc validation stabilitystudies hplc gc regulatoryaudits analytical methoddevelopment varianceanalysis operations daJob Description and responsibilities; - Capabilities: In- depth understanding of GMPs, US FDA, MHRA UK, EU, ANVISA Brazil, TGA Australia, MCC South Africa, ICH Regulatory guidelines. Should have exp...
nalytical research continuous improvement facilitationJob Description and responsibilities; - Capabilities: Thorough understanding and on- hand experience in Analytical Method Development, Validation and Stability Studies as per EU/ US requirements. Ha...
documentation research nalyticalmethoddevelopment methoddevelopmentThorough understanding and on- hand experience in Analytical Method Development, Validation and Stability Studies as per EU/ US requirements. Having thorough knowledge of impurity profiling, dissoluti...
operations ethoddevelopment regulatoryaudits analyticalmethoddevelopmentCapabilities: Thorough understanding and on-hand experience in Analytical Method Development, Validation and Stability Studies as per EU/US requirements. Having thorough knowledge of impurity profilin...
ethod development analytical method development
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