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B.Sc / M.Sc. / BE Chem Engg. / Dip Chem Engg. 08 10 years Exposure in API domain , conversant with regulatory requirements & documentation. Preferred FDA approved - mfg API.,...
bsc api fda mfg ElectronicCommonTechnicalDocument CommonTechnicalDocument NeeS CMC egulat yrequirements regulat CMCRegulat yAffairs Regulat yIntelligence Regulat yStrategyDevelopment AbbreviatedNewDrugPeoplsoft Finance Tester Experienced PeopleSoft Finance testers Should have work experience in International processes, multicurrency etc. Also should have experience in regulatory requirements such...
peoplesoftfinance regulatoryrequirements vat finance testing testers peoplesoft regulatory ElectronicCommonTechnicalDocument CommonTechnicalDocument NeeS CMCRegulatoryAffairs MCQualified pharmacist0 to 5 years experience in retail pharmacy with good knowledge of pharmacy brands & regulatory affairs with good communication skills. ,...
retail communication ElectronicCommonTechnicalDocument AbbreviatedNewDrugApplication GenericProgramming CommonTechnicalDocument IND egulat yaffairs regulat Regulat ySubmissions CMCRegulat yAffairs ReguB.Sc / M.Sc. / BE Chem Engg. / Dip Chem Engg. 08 10 years Exposure in API domain , conversant with regulatory requirements & documentation. Preferred FDA approved - mfg API.,...
bsc api fda mfg ElectronicCommonTechnicalDocument CommonTechnicalDocument NeeS CMC egulat yrequirements regulat CMCRegulat yAffairs Regulat yIntelligence Regulat yStrategyDevelopment AbbreviatedNewDrugQualified pharmacist0 to 5 years experience in retail pharmacy with good knowledge of pharmacy brands & regulatory affairs with good communication skills. ,...
regulatoryaffairs retail regulatory communication ElectronicCommonTechnicalDocument RegulatorySubmissions AbbreviatedNewDrugApplication GenericProgramming CMCRegulatoryAffairs CommonTechnicalDocument RegulatoryRequirements StoreManagement VisuManager/ Sr.Manager Production 08 10 years Predominantly API exposure. Exposure to USFDA Audit, GMP and cGMP guide lines, Exposure to Regulatory affairs & Compliance activities ,...
api gmp cgmp usfda compliance ElectronicCommonTechnicalDocument AbbreviatedNewDrugApplication GenericProgramming CommonTechnicalDocument egulat yaffairs regulat Regulat ySubmissions CMCRegulat yAffairs2.Regulatory Affairs: Incumbent Should be a M.Pharm(Regulatory Affairs) with 1 to 3 years experience in ROW Market.,...
regulatoryaffairs regulatory ElectronicCommonTechnicalDocument RegulatorySubmissions AbbreviatedNewDrugApplication GenericProgramming CMCRegulatoryAffairs CommonTechnicalDocument RegulatoryRequirements RegulatoryRisk FederalRegulations SanctionExp in Regulatory filings (US/EU) (API) (Global Market), Compilation of Regulatory Documents (USDMFs, ANDAs) in CTD & eCTD format, Review of in-house Dossiers as per Good Regulatory Practices for its ...
regulatoryaffairs regulatoryfilings ctd sound regulatory compilation ElectronicCommonTechnicalDocument RegulatorySubmissions AbbreviatedNewDrugApplication GenericProgramming CMCRegulatoryAffairs CommonTechnicalDocument RegulatoryRequirements
Development of different formulations either as generic or differentiated generics. To demonstrate successful stability and scale up at manufacturing site.
Core Job Responsibilities
D...
Assistant Manager - Hyderabad Description: eCTD experience, queries / deficiencies response writing, review of CMC data and DMF, follow up capability with internal departments planning and execution ...
sales mis accounts tat banking cmc dmf writing planning IMPD NewDrugApplication CommonTechnicalDocument CMCdevelopment MAA NeeS MCRegulat yAffairs Regulat yIntelligence Regulat yStrategyDevelopment DossiQualified pharmacist0 to 5 years experience in retail pharmacy with good knowledge of pharmacy brands & regulatory affairs with good communication skills. ,...
retail communication ElectronicCommonTechnicalDocument AbbreviatedNewDrugApplication GenericProgramming CommonTechnicalDocument IND egulat yaffairs regulat Regulat ySubmissions CMCRegulat yAffairs ReguAssistant Manager - Hyderabad Description: eCTD experience, queries / deficiencies response writing, review of CMC data and DMF, follow up capability with internal departments planning and execution ...
sales mis accounts tat banking cmc dmf writing planning IMPD NewDrugApplication CommonTechnicalDocument CMCdevelopment MAA NeeS MCRegulat yAffairs Regulat yIntelligence Regulat yStrategyDevelopment DossiQualified pharmacist0 to 5 years experience in retail pharmacy with good knowledge of pharmacy brands & regulatory affairs with good communication skills. ,...
retail communication ElectronicCommonTechnicalDocument AbbreviatedNewDrugApplication GenericProgramming CommonTechnicalDocument IND egulat yaffairs regulat Regulat ySubmissions CMCRegulat yAffairs ReguManager/ Sr.Manager Production 08 10 years Predominantly API exposure. Exposure to USFDA Audit, GMP and cGMP guide lines, Exposure to Regulatory affairs & Compliance activities ,...
api gmp cgmp usfda compliance ElectronicCommonTechnicalDocument AbbreviatedNewDrugApplication GenericProgramming CommonTechnicalDocument egulat yaffairs regulat Regulat ySubmissions CMCRegulat yAffairsB.Sc / M.Sc. / BE Chem Engg. / Dip Chem Engg. 03 04 years Exposure in API domain , conversant with regulatory requirements & documentation. Preferred FDA approved - mfg API.,...
bsc api fda mfg ElectronicCommonTechnicalDocument CommonTechnicalDocument NeeS CMC egulat yrequirements regulat CMCRegulat yAffairs Regulat yIntelligence Regulat yStrategyDevelopment AbbreviatedNewDrugB.Sc / M.Sc. / BE Chem Engg. / Dip Chem Engg. 08 10 years Exposure in API domain , conversant with regulatory requirements & documentation. Preferred FDA approved - mfg API.,...
bsc api fda mfg ElectronicCommonTechnicalDocument CommonTechnicalDocument NeeS CMC egulat yrequirements regulat CMCRegulat yAffairs Regulat yIntelligence Regulat yStrategyDevelopment AbbreviatedNewDrugDescription: eCTD experience, compilation of DMF, review of CMC data. Experience Required: 2 - 4 Years Location: Hyderabad Department: RA Unit: RA Salary: At par within industry,...
cmc dmf compilation IMPD NewDrugApplication CommonTechnicalDocument CMCdevelopment MAA NeeS DossierPreparation BMR DCP MCRegulat yAffairs Regulat yIntelligence Regulat yStrategyDevelopment EntitySelectiAssistant Manager - Hyderabad Description: eCTD experience, queries / deficiencies response writing, review of CMC data and DMF, follow up capability with internal departments planning and execution ...
sales mis accounts tat banking cmc dmf writing planning IMPD NewDrugApplication CommonTechnicalDocument CMCdevelopment MAA NeeS MCRegulat yAffairs Regulat yIntelligence Regulat yStrategyDevelopment DossiDescription: eCTD experience, queries / deficiencies response writing, review of CMC data and DMF, follow up capability with internal departments, planning of day to day activities. Experience Requi...
mis sales customerrelations customerservice delivery cmc dmf writing planning IMPD NewDrugApplication CommonTechnicalDocument CMCdevelopment MAA MCRegulat yAffairs Regulat yIntelligence Regulat yStrategDescription: eCTD experience, queries / deficiencies response writing, review of CMC data and compilation of DMF, follow up of internal departments. Experience Required: 3 - 6 Years Location: Hyder...
mis sales customerrelations customerservice delivery cmc dmf writing compilation IMPD NewDrugApplication CommonTechnicalDocument CMCdevelopment MAA MCRegulat yAffairs Regulat yIntelligence Regulat yStraUnder moderate supervision:
Description: eCTD experience, queries / deficiencies response writing, review of CMC data and compilation of DMF, follow up of internal departments. Experience Required: 3 - 6 Years Location: Hyder...
missalescustomerrelationscustomerservicedeliverycmcdmfwritingcompilationIMPDNewDrugApplicationCommonTechnicalDocumentCMCdevelopmentMAAMCRegulatyAffairsRegulatyIntelligenceRegulatyStraAssistant Manager - Hyderabad Description: eCTD experience, queries / deficiencies response writing, review of CMC data and DMF, follow up capability with internal departments planning and execution ...
salesmisaccountstatbankingcmcdmfwritingplanningIMPDNewDrugApplicationCommonTechnicalDocumentCMCdevelopmentMAANeeSMCRegulatyAffairsRegulatyIntelligenceRegulatyStrategyDevelopmentDossiDescription: eCTD experience, queries / deficiencies response writing, review of CMC data and DMF, follow up capability with internal departments, planning of day to day activities. Experience Requi...
missalescustomerrelationscustomerservicedeliverycmcdmfwritingplanningIMPDNewDrugApplicationCommonTechnicalDocumentCMCdevelopmentMAAMCRegulatyAffairsRegulatyIntelligenceRegulatyStrategDescription: eCTD experience, compilation of DMF, review of CMC data. Experience Required: 2 - 4 Years Location: Hyderabad Department: RA Unit: RA Salary: At par within industry,...
cmcdmfcompilationIMPDNewDrugApplicationCommonTechnicalDocumentCMCdevelopmentMAANeeSDossierPreparationBMRDCPMCRegulatyAffairsRegulatyIntelligenceRegulatyStrategyDevelopmentEntitySelectiTo be responsible for the credit administration related work. Key Accountabilities
Perform and document results of regularly scheduled laboratory tests Assist in new product development and improvements of existing products Perform entry-level testing and comparison of experimental ...
streamschemistrypharmaceuticsresumepharmacognosyassurancepharmacologyregulatoryschedulemcregulatoryaffairsregulatorysubmissionsqualityassuranceregulatoryaffairscommontechnicaldocumentgenericprogrammingabbreviatednewdrugapplicationelectroniPerform and document results of regularly scheduled laboratory tests Assist in new product development and improvements of existing products Perform entry-level testing and comparison of experimental ...
streamschemistrypharmaceuticsresumepharmacognosyassurancepharmacologyregulatoryschedulemcregulatoryaffairsregulatorysubmissionsqualityassuranceregulatoryaffairscommontechnicaldocumentgenericprogrammingabbreviatednewdrugapplicationelectroniCandidate should have knowledge of pharma. Chemical , Food with good knowledge of communication skills Innovate bent of mind Analytical and Problem solving skills Vacancy:02 Venue: Company:Autosyste...
streamschemistryindpharmaceuticsvizpharmacognosyassurancepharmacologyregulatorymcregulatoryaffairsregulatorysubmissionsqualityassuranceregulatoryaffairscommontechnicaldocumentgenericprogrammingabbreviatednewdrugapplicationelectroniccommont1. Handling a team BE (Business Executives) 2. Responsible for Business Achievement for their assigned Head Quarters. 3. Meet the doctors (along with their BE if required) to introduce the company b...
streamschemistryindpharmaceuticsvizpharmacognosyassurancepharmacologyregulatoryschedulemcregulatoryaffairsregulatorysubmissionsqualityassuranceregulatoryaffairscommontechnicaldocumentgenericprogrammingabbreviatednewdrugapplicationelectronPerform and document results of regularly scheduled laboratory tests Assist in new product development and improvements of existing products Perform entry-level testing and comparison of experimental ...
streamschemistrypharmaceuticsresumepharmacognosyassurancepharmacologyregulatoryschedulemcregulatoryaffairsregulatorysubmissionsqualityassuranceregulatoryaffairscommontechnicaldocumentgenericprogrammingabbreviatednewdrugapplicationelectroni1. Handling a team BE (Business Executives) 2. Responsible for Business Achievement for their assigned Head Quarters. 3. Meet the doctors (along with their BE if required) to introduce the company b...
streamschemistryindpharmaceuticsvizpharmacognosyassurancepharmacologyregulatoryschedulemcregulatoryaffairsregulatorysubmissionsqualityassuranceregulatoryaffairscommontechnicaldocumentgenericprogrammingabbreviatednewdrugapplicationelectron-Preparation of Doctors List -Doctor/Product selection through Chemist Survey -Regular coverage of customers with right frequency -Have a track of liquidation of stock of assigned territories. Vacanc...
streamschemistryindpharmaceuticsvizpharmacognosyassurancepharmacologyregulatoryschedulemcregulatoryaffairsregulatorysubmissionsqualityassuranceregulatoryaffairscommontechnicaldocumentgenericprogrammingabbreviatednewdrugapplicationelectronCandidate will be responsible for Sales & Business development activities. Relationship building with doctors and hospitals Will have to maintain regularity in relationship building Do chemist survey ...
chemistryschedulepharmaceuticsstreamspharmacologyregulatorypharmacognosyassurancebbreviatednewdrugapplicationcommontechnicaldocumentdrugregulatoryaffairscmcregulatoryaffairsgenericprogrammingregulatorysubmissionsqualityassuranceregulatoryafCandidate will be responsible for Sales & Business development activities. Relationship building with doctors and hospitals Will have to maintain regularity in relationship building Do chemist survey ...
chemistryschedulepharmaceuticsstreamspharmacologyregulatorypharmacognosyassurancebbreviatednewdrugapplicationcommontechnicaldocumentdrugregulatoryaffairscmcregulatoryaffairsgenericprogrammingregulatorysubmissionsqualityassuranceregulatoryaf1. Handling a team BE (Business Executives) 2. Responsible for Business Achievement for their assigned Head Quarters. 3. Meet the doctors (along with their BE if required) to introduce the company b...
streamschemistryindpharmaceuticsvizpharmacognosyassurancepharmacologyregulatoryschedulemcregulatoryaffairsregulatorysubmissionsqualityassuranceregulatoryaffairscommontechnicaldocumentgenericprogrammingabbreviatednewdrugapplicationelectron© 2019 Hireejobs All Rights Reserved