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Roles and Responsibilities Managing Operations, overall functioning of the branch. Responsible for meeting the branch targets and adherence to all guidelines and regulatory requirements Cost ...
operationsabbreviated new drug applicationcmc regulatory affairscompliancesalesneescommon technical documentregulatory requirementscustomer servicebankingcost managementelectronic common technical documentadherenceregulatory intelligencereguPosition : Regulatory Affairs - API ( US ,Europe and CEP Markets) To write, check/review of documents as per regulatory requirements To publish with software submission documentation as per regulato...
new drug applicationrisk analysisin-licensingelectronic common technical documentdocumentationcommon technical documentregulatory intelligenceregulatory requirementsneesabbreviated new drug applicationregulatorycmc regulatory affairsregulatJob location is Mumbai Prior exp in BFSI legal will be added advantage Job entails an in-house legal counsel at the group level. It requires a good understanding and interpretations of the r...
advcompliancefilingregulatory strategy developmentdraftingcommunication skillsregulatory intelligencecustodyagreementsregulatoryregulationsbusinessneescftcbfsiregulatory filingsnbfcRoles and Responsibilities Managing Operations, overall functioning of the branch. Responsible for meeting the branch targets and adherence to all guidelines and regulatory requirements Cost ...
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The OIM is responsible for ensuring the safe operation of an offshore production installation which may be an offshore platform or production vessel, whilst also optimising production through complian...
regulatory requirementscommunicationoptimisingacrylicadditionmanagementregulatoryinspectionoiminstallationsiteelectronic common technical documentbaggage handlingcomplianceoffshoreneeswelfarecommon technical documentThe OIM is responsible for ensuring the safe operation of an offshore production installation which may be an offshore platform or production vessel, whilst also optimising production through complian...
regulatory requirementscommunicationoptimisingacrylicadditionmanagementregulatoryinspectionoiminstallationsiteelectronic common technical documentbaggage handlingcomplianceoffshoreneeswelfarecommon technical documentThe OIM is responsible for ensuring the safe operation of an offshore production installation which may be an offshore platform or production vessel, whilst also optimising production through complian...
regulatory requirementscommunicationoptimisingacrylicadditionmanagementregulatoryinspectionoiminstallationsiteelectronic common technical documentbaggage handlingcomplianceoffshoreneeswelfarecommon technical documentThe OIM is responsible for ensuring the safe operation of an offshore production installation which may be an offshore platform or production vessel, whilst also optimising production through complian...
regulatory requirementscommunicationoptimisingacrylicadditionmanagementregulatoryinspectionoiminstallationsiteelectronic common technical documentbaggage handlingcomplianceoffshoreneeswelfarecommon technical documentThe OIM is responsible for ensuring the safe operation of an offshore production installation which may be an offshore platform or production vessel, whilst also optimising production through complian...
regulatory requirementscommunicationoptimisingacrylicadditionmanagementregulatoryinspectionoiminstallationsiteelectronic common technical documentbaggage handlingcomplianceoffshoreneeswelfarecommon technical documentRoles 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 registrationspecialist_regulatory submissions in chennai PL of Publishing team, assigning of publishing tasks to the team members andupdate the trackers. To Pr...
digital conversionchartered property casualty underwriter cpcuclient requirementapi regulatory affairs manager in gurgaon Managerail experience in Must into API * Compilation, preparation, and review of DMFs for US, Europe, Can...
vendorfilingcosmeticsregulatory agenciesdmfneesregulatoryprocess developmentusfdaregulatory affairsapiichrecord keepingcompliancerecordsctdcmcdrugs cosmeticsThe OIM is responsible for ensuring the safe operation of an offshore production installation which may be an offshore platform or production vessel,...
oimregulatory intelligenceregulatory requirementsoptimisingelectronic common technical documentairportsneesacrylicinspectionoffshorebaggage handlingcompliancesitecmc regulatory affairsregulatory strategy developmentregulatorycommunicationThe OIM is responsible for ensuring the safe operation of an offshore production installation which may be an offshore platform or production vessel,...
oimregulatory intelligenceregulatory requirementsoptimisingelectronic common technical documentairportsneesacrylicinspectionoffshorebaggage handlingcompliancesitecmc regulatory affairsregulatory strategy developmentregulatorycommunicationThe OIM is responsible for ensuring the safe operation of an offshore production installation which may be an offshore platform or production vessel,...
oimregulatory intelligenceregulatory requirementsoptimisingelectronic common technical documentairportsneesacrylicinspectionoffshorebaggage handlingcompliancesitecmc regulatory affairsregulatory strategy developmentregulatorycommunicationThe OIM is responsible for ensuring the safe operation of an offshore production installation which may be an offshore platform or production vessel,...
electronic common technical documentinstallationcmc regulatory affairsregulatory requirementsregulatorycompliancecommunicationneesacrylicinspectionregulatory strategy developmentairportsbaggage handlingoimoffshorecommon technical documentThe OIM is responsible for ensuring the safe operation of an offshore production installation which may be an offshore platform or production vessel,...
electronic common technical documentinstallationcmc regulatory affairsregulatory requirementsregulatorycompliancecommunicationneesacrylicinspectionregulatory strategy developmentairportsbaggage handlingoimoffshorecommon technical documentThe OIM is responsible for ensuring the safe operation of an offshore production installation which may be an offshore platform or production vessel,...
electronic common technical documentinstallationcmc regulatory affairsregulatory requirementsregulatorycompliancecommunicationneesacrylicinspectionregulatory strategy developmentairportsbaggage handlingoimoffshorecommon technical documentLead Consultant, Publishing In this role, you will be responsible to work on deadlines, in a fairly high pressure business environment while being a good team member. You should have...
sapenvironmentdeliverycustomer relationssalesmusic makinghigh pressurecustomer focusproblem solvingtime managementanalytical skillscustomer handlingProfessional 2 Life Sciences BPS Experience: 7+ years of Regulatory Publishing Job Location: Hyderabad
Lead Consultant - Regulatory Affairs - CPG019712 With a startup spirit and 90,000+ curious and courageous minds, we have the expertise to go deep with the world s biggest brands and we have fun doing...
sapdeliveryproduct life cycle managementmusic makingenvironmentproblem solvingcustomer focusproduct life cyclepostinglife cycletime managementsalescustomer relationsstatements of work sowRoles and Responsibilities :- Urgently required Company Secretary for renowned Realestate Developer located at Mumbai. To take care of companys legal compliances. Co-ordinates for the company and ma...
rocdocumentationapprovalsagendaregulatory requirementsmanagementneesstatutorycommon technical documentsecretarial compliancecarefemarbicompliancecmc regulatory affairsreturnsstatutory complianceregulatoryelectronic common technical documB.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.,...
bscapifdamfgElectronic Common Technical DocumentCommon Technical DocumentNeeSCMCregulaty requirementsregulatCMC Regulaty AffairsRegulaty IntelligenceRegulaty Strategy DevelopmentAbbreviated New DrugLead Associate, Publishing
We are inviting applications for the role of Business Analyst, Publishing! In this role, you will be responsible to work on deadlines, in a fairly high pressure business environment while bein...
customer relationsdocumentationrequirementsfunctionalbusiness requirementspostingmusic makinghigh pressurecustomer focusstatements of work sowSM, Regulatory Affairs! In this role, you are expected to have good knowledge of Planning and timely execution of product life cycle management projects. We are looking for some who should be o...
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AM, CMC PA Changes In this role, you will work on ICH guidelines and CTD Structure & Expertise with Publishing Tools like Liquent , Docubridge, etc. Responsibilities <...
salesmisaccountstatbankingms officepostingmusic makingcustomer focusdigital conversioncommunication skillsverbal communicationWorks effectively within a team environment but may work independently delivering services within their area of competence Must be able to work independently on submissions, mentor publishers and pro...
clinical trialsdocumentationapacdcgisopadobe acrobatmicrosoft officemanagement systemsdigital conversiondocument managementsoftware validationneeswindowsdesktopsoftwareadobeWorks effectively within a team environment but may work independently delivering services within their area of competence Must be able to work independently on submissions, mentor publishers and pro...
clinical trialsdocumentationapacdcgisopadobe acrobatmicrosoft officemanagement systemsdigital conversiondocument managementsoftware validationneeswindowsdesktopsoftwareadobeWorks effectively within a team environment but may work independently delivering services within their area of competence Must be able to work independently on submissions, mentor publishers and pro...
clinical trialsdocumentationapacdcgisopadobe acrobatmicrosoft officemanagement systemsdigital conversiondocument managementsoftware validationneeswindowsdesktopsoftwareadobeWorks effectively within a team environment but may work independently delivering services within their area of competence Must be able to work independently on submissions, mentor publishers and pro...
clinical trialsdocumentationapacdcgisopadobe acrobatmicrosoft officemanagement systemsdigital conversiondocument managementsoftware validationneeswindowsdesktopsoftwareadobe
Job description : Handling of country audits. Not less than 10 years of experience in Pharmaceutical Industry. Conversant with local and international regulatory Guidelines and GMP requirements. Candi...
regulatoryRegulatory AgenciesNeeSRegulatory IntelligenceRegulatory DocumentationRegulatory PolicyRegulatory Strategy DevelopmentRegulatory OperationsDossier PreparationRegulatory FilingsMarket AccessB.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.,...
bscapifdamfgElectronic Common Technical DocumentCommon Technical DocumentNeeSCMCregulaty requirementsregulatCMC Regulaty AffairsRegulaty IntelligenceRegulaty Strategy DevelopmentAbbreviated New Drug- Responsible for compilation and review of dossier for a product for the regulated markets and customers - Circulate checklist for dossier requirements - Coordinate with R&D, QA, QC and productio...
annual reportsandaneessoftwarecompilationAnnual MeetingsPrint CollateralAnnual ReviewsAnnual PlanningQuarterly ReportingLetterheadBookletsPostcardsAnnual BudgetsGxPChange ControlQuality AuditingDevelopment 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 TechniB.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.,...
bscapifdamfgElectronic Common Technical DocumentCommon Technical DocumentNeeSCMCregulaty requirementsregulatCMC Regulaty AffairsRegulaty IntelligenceRegulaty Strategy DevelopmentAbbreviated New Drug© 2019 Hireejobs All Rights Reserved