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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...
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 CommonTechniExecutive/ Sr. Executive - Quality Assurance Desired Eligibility Pharma. Graduate and/ or Post- Graduate Minimum 1 5 years of same area. Candidates having similar experience in production or quality c...
drugtesting rawmaterials qualitycontrol processquality productquality printbrokering packingmaterial materialcontrol qualityassurance finishedproducts marketcomplaints dtp spc egulat ydocumentationKnowledge of Oral and Injectable dosage forms. Handling of Tablets, Capsules, Oral Liquids and Oral Suspensions. Handling of Injectable Liquid and Lyophilized Formulations. Knowledge about the handlin...
research validation hplc documentation calibration glp tablets capsules injectable NeeS egulat yguidelines regulat Regulat yAgencies Regulat yIntelligence Regulat yDocumentation Regulat yPolicy Regulat yStraHandling of Tablets, Capsules, Oral Liquids and Oral Suspensions. Handling of Injectable Liquid and Lyophilized Formulations. Knowledge about the handling of Cytotoxic materials. Knowledge about the s...
research validation hplc documentation calibration glp tablets capsules injectable NeeS egulat yguidelines regulat Regulat yAgencies Regulat yIntelligence Regulat yDocumentation Regulat yPolicy Regulat yStraResearch Associate / Sr. Research Associate - Formulations R&D Department name R&D Position Name Research Associate / Sr. Research Associate M.Pharmacy (Pharmaceutics/ Industrial Pharmacy) Age Limit 3...
research validation hplc documentation calibration glp tablets capsules injectable NeeS egulat yguidelines regulat Regulat yAgencies Regulat yIntelligence Regulat yDocumentation Regulat yPolicy Regulat yStraResearch Associate / Sr. Research Associate - Formulations R&D Department name R&D Position Name Research Associate / Sr. Research Associate M.Pharmacy (Pharmaceutics/ Industrial Pharmacy) Age Limit 3...
research validation hplc documentation calibration glp tablets capsules injectable NeeS egulat yguidelines regulat Regulat yAgencies Regulat yIntelligence Regulat yDocumentation Regulat yPolicy Regulat yStraKnowledge of Oral and Injectable dosage forms. Handling of Tablets, Capsules, Oral Liquids and Oral Suspensions. Handling of Injectable Liquid and Lyophilized Formulations. Knowledge about the handlin...
research validation hplc documentation calibration glp tablets capsules injectable NeeS egulat yguidelines regulat Regulat yAgencies Regulat yIntelligence Regulat yDocumentation Regulat yPolicy Regulat yStraDevelopment 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 CommonTechniHandling of Tablets, Capsules, Oral Liquids and Oral Suspensions. Handling of Injectable Liquid and Lyophilized Formulations. Knowledge about the handling of Cytotoxic materials. Knowledge about the s...
research validation hplc documentation calibration glp tablets capsules injectable NeeS egulat yguidelines regulat Regulat yAgencies Regulat yIntelligence Regulat yDocumentation Regulat yPolicy Regulat yStraResearch Associate / Sr. Research Associate - Formulations R&D Department name R&D Position Name Research Associate / Sr. Research Associate M.Pharmacy (Pharmaceutics/ Industrial Pharmacy) Age Limit 3...
research validation hplc documentation calibration glp tablets capsules injectable NeeS egulat yguidelines regulat Regulat yAgencies Regulat yIntelligence Regulat yDocumentation Regulat yPolicy Regulat yStraExecutive/ Sr. Executive - Quality Assurance Desired Eligibility Pharma. Graduate and/ or Post- Graduate Minimum 1 5 years of same area. Candidates having similar experience in production or quality c...
drugtesting rawmaterials qualitycontrol processquality productquality printbrokering packingmaterial materialcontrol qualityassurance finishedproducts marketcomplaints dtp spc egulat ydocumentationM.Sc. , M.Pharm. , B.Pharm. with mnimum 15 years of experience in related field. Ensuring compliance to cGMP , GDP for plant operations. Successfully managed Regulated and Semi- regulated market audi...
cgmp attrition compliance directives NeeS egulat yguidelines regulat Regulat yAgencies Regulat yIntelligence Regulat yDocumentation Regulat yPolicy Regulat yStrategyDevelopment Regulat yOperations DossieM.Sc. , M.Pharm. , B.Pharm. with mnimum 15 years of experience in related field. Ensuring compliance to cGMP , GDP for plant operations. Successfully managed Regulated and Semi- regulated market audi...
cgmp attrition compliance directives NeeS egulat yguidelines regulat Regulat yAgencies Regulat yIntelligence Regulat yDocumentation Regulat yPolicy Regulat yStrategyDevelopment Regulat yOperations Dossie274754BR Sr. Executive MRC Job Description Position Purpose Provide and ensure timely preparation of high quality CMC regulatory documentation and support in line with global regulatory submissio...
continuousimprovementfacilitationlifecycledigitalconversioncmcsagesoundanicchemistryregulatyaffairsregulatycomplianceregulatyguidelinesregulatysubmissionsregulatydocumentationageM.Sc. , M.Pharm. , B.Pharm. with mnimum 15 years of experience in related field. Ensuring compliance to cGMP , GDP for plant operations. Successfully managed Regulated and Semi - regulated market aud...
cgmpattritioncompliancedirectivesNeeSegulatyguidelinesregulatRegulatyAgenciesRegulatyIntelligenceRegulatyDocumentationRegulatyPolicyRegulatyStrategyDevelopmentRegulatyOperationsDossieResearch Associate / Sr. Research Associate - Formulations R&D Department name R&D Position Name Research Associate / Sr. Research Associate M.Pharmacy (Pharmaceutics/ Industrial Pharmacy) Age Limit 3...
researchvalidationhplcdocumentationcalibrationglptabletscapsulesinjectableNeeSegulatyguidelinesregulatRegulatyAgenciesRegulatyIntelligenceRegulatyDocumentationRegulatyPolicyRegulatyStraHandling of Tablets, Capsules, Oral Liquids and Oral Suspensions. Handling of Injectable Liquid and Lyophilized Formulations. Knowledge about the handling of Cytotoxic materials. Knowledge about the s...
researchvalidationhplcdocumentationcalibrationglptabletscapsulesinjectableNeeSegulatyguidelinesregulatRegulatyAgenciesRegulatyIntelligenceRegulatyDocumentationRegulatyPolicyRegulatyStraKnowledge of Oral and Injectable dosage forms. Handling of Tablets, Capsules, Oral Liquids and Oral Suspensions. Handling of Injectable Liquid and Lyophilized Formulations. Knowledge about the handlin...
researchvalidationhplcdocumentationcalibrationglptabletscapsulesinjectableNeeSegulatyguidelinesregulatRegulatyAgenciesRegulatyIntelligenceRegulatyDocumentationRegulatyPolicyRegulatyStra© 2019 Hireejobs All Rights Reserved