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SALARY: up to 4 Lakhs LOCATION : Hyderabad, Telangana, India VACANCIES: 1 QUALIFICATION: B.E. Mechancal MALE/FEMALE: Male ...
internal auditplant expansionequipment supplyintelligent networksapiqmsfuelmhrausfdapharmaagencySALARY: 25-30K VACANCIES: 1 QUALIFICATION: B E Mechanic MALE/FEMALE: Male EXPERIENCE: 3-7 years JOB DETAILS 1...
mechanicalinspectionsafetysitecommissioninginternal auditplant expansionregulatory auditscontrol engineeringintelligent networksapiqmsmhrausfdapharmaagencycontrolvendorsplacementoperations Hiring for well known Pharma Industry Pithampur/ Indore
Job Profile - Production / QC /QA / MICROBIOLOGIST /R&D / PRODUCTION MANAGER
Experience - Fresher to 12 Years
...
Capabilities: 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 validationJob 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 DocumentfdamedicalQualifications: 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 analysisoperationsfdaAny Graduate/ Post Graduate with 1- 2 years of IT experience in Java and related areas with SQL knowlegde in any of the databases We prefer enthusiastic learners willing to adapt to new and demanding...
fdaedctroubleshootingcdmsqljavadata managementsql servermanagement servicesmanagement systemclinical triallaboratory information management systeminformation management
Ensuring compliance with regulations set by the Medicines and Healthcare products Regulatory Agency (MHRA) Maintaining familiarity with company product ranges Providing advice about regulations to m...
draftinglegalcompliancefilinglegislative relationssetagencyhealthcarenegotiationregulationsdocumentationAppropriationsCoalitionsLegislative AffairsConstituent ServicesexpregulatLegislative Researc
Visakhapatnam To follow and implement the systems, procedures and practices for packaging operations and execution of production packing plan. READ MORE Drug Product Manufacturing - Packing Drug Produ...
shop floorteam buildingfloor planningquality controlmedical affairsquality assurancemanpower handlingmarket complaintspackaging operationsregulatory guidelinesregulatory requirementsSound 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 OrganizationsDemocracyregulatTransatlanhead - quality in mumbai Responsibilities: - Lead the Quality function at site and ensure that the site meets local and international regulatory requirements and remains incompliance to cGMP at all t...
quality management systemquality systems customer auditssenior management service providersmanagement system management reviewHiring for well known Pharma Industry Pithampur/ Indore Job Profile -Production Experience - Fresher to 12 Years Education- Any Graduate (B Pharma, M Pharma, BSC or MSC ) Salary - 2.0- 5.90 L/ A (...
pharmachemistryKnowledge 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 TransatlanOrganize appointments & meetings with Healthcare Professionals (HCP) to promote company products and generate prescriptions. Achieve assigned sales targets and identify new business opportunities. E...
conferences research client consulting keyskills newbusiness marketcomm top nowVisakhapatnam To follow and implement the systems, procedures and practices for packaging operations and execution of production packing plan. READ MORE Drug Product Manufacturing - Packing Drug Produ...
shop floorteam building floor planningquality control medical affairsquality assurance manpower handlingmarket complaintsQualifications: 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 developmentOpenings Executive (QC) - M.Sc / B. Sc (Chem) HPLC MUST Executive (QC- Microbilogy) : 3 to 9 Yrs Executive QA -Formulation (USFDA) - M.Sc Sr Executive -Engineering (API) Asst. Mgr - Production (S...
qualitycontrol qualityassurance qa qc sc bsc api hplc mhra usfda pharma salary control openings assurance injectable microbiology RadiographicTesting NDE SPharmacopeiaPosition - DGM - Corporate Engineering Location Corporate Office, Mumbai Reporting to Head Engineering & Projects Team Size 1 Position Overview Res...
continuous improvement facilitationinternal audit problem solvingregulatory audits working experienceapi gmppharmaCapabilities: 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...
analytical kaizen regulatory research filing ootcauseanalysis analyticalresearch continuousimprovementfacilitation pharmaresearch continuousimprovementcultureJob 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 methoddevelopmentCapabilities: 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 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...
nalytical research continuous improvement facilitationCapabilities: 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 daThorough 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 analyticalmethoddevelopmentVisakhapatnam To follow and implement the systems, procedures and practices for packaging operations and execution of production packing plan. READ MORE Drug Product Manufacturing - Packing Drug Produ...
shop floorteam building floor planningquality control medical affairsquality assurance manpower handlingmarket complaintsJob Title Packing Development and Operations Position Associate Manager Required Educational Qualification M. Pharm or B.Pharm having 9-12 years of experience in pharmaceutical packing developmen...
regulatory compliancepharmaceutical packaging packaging developmentcontinuous improvement facilitation change controlquality systemJob Title Packing Development and Operations Position Associate Manager Required Educational Qualification M. Pharm or B.Pharm having 9-12 years of experience in pharmaceutical packing developmen...
regulatory compliancepharmaceutical packaging packaging developmentcontinuous improvement facilitation change controlquality systemJob Title Packing Development and Operations Position Associate Manager Required Educational Qualification M. Pharm or B.Pharm having 9-12 years of experience in pharmaceutical packing developmen...
regulatory compliancepharmaceutical packaging packaging developmentcontinuous improvement facilitation change controlquality systemJob Title Packing Development and Operations Position Associate Manager Required Educational Qualification M. Pharm or B.Pharm having 9-12 years of experience in pharmaceutical packing developmen...
regulatory compliancepharmaceutical packaging packaging developmentcontinuous improvement facilitation change controlquality system© 2019 Hireejobs All Rights Reserved