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3- 4 years of experience in Regulatory submission for US market Description RESPONSIBILITIES: Ensure timely submission of dossiers in US and Canada. Ensure timely submission of ...
validation adherence internetexplorer chemistry annualreports ownership lifecycle regulatoryaffairs oncology api management hplc compliancemanagement maintenanceactivities pharma regulatory compliance research firefox mcDescription: Global Compliance and Reporting is an integrated suite of Tax and Accounting services that EY provides to our multinational clients. GCR offers the ease of managing compliance & regulato...
servicelevel teammanagement servicedelivery globalcompliance projectmanagement regulatoryaffairs servicemanagement regulatoryfilings clientrequirements engagementmanagement tatementsofworksow offshoreteams
Manager - Regulatory Affairs 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 it. Now, we re call...
handlemultiplepriorities environmentalimpactassessment qualityassurance regulatoryissues regulatoryaffairs analyticaltesting pharmaceuticalmanufacturing go visit color testing mcExecutive - Regulatory Affairs Qualification: Msc/ Btech- Biotchnology/ Toxicology/ Microbiology Skills Require: Good communication skill, good in word & Excel, Internet savvy. Compilation of registr...
regulatoryaffairs scientificreports gc word msds excel testing analysis regulatory toxicology microbiology registration communication ElectronicCommonTechnicalDocument RegulatorySubmissions AbbreviatedNewDrugApplication GenericProgramming
SALARY: 3LPA - 4LPA VACANCIES: 1 QUALIFICATION: B.Pharma/ Bsc MALE/FEMALE: Both EXPERIENCE: 2yr - 4yr JOB DETAILS<...
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tKeywords: Financial/ Regulatory Reporting, Regulatory Affairs,R2R. tLevel wise Experience:1. tOperations Manager Post CA 10 yearsu2019 Experience (excluding Article ship)Process Improvements , Change...
recordtoreport teamhandling generalledger changemanagement peoplemanagement regulatoryaffairs regulatoryreporting gl r2r rtr ledger taxation reporting management regulatory communication FA ProcessOrientation AOperationsQualified 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 Visu
Description of the Role:
RESPONSIBILITIES: Manage all aspects of the regulatory process for US and Canada submissions, viz, review and submission of the marketing authorization application, timely and satisfactory response to...
planning marketing database approvals strategy egulatoryapprovals technologytransfer regulatoryaffairs regulatoryrequirements productdevelopment formulationdevelopment projectteamsExecutive - Regulatory Affairs Qualification: Msc/ Btech- Biotchnology/ Toxicology/ Microbiology Skills Require: Good communication skill, good in word & Excel, Internet savvy. Compilation of registr...
regulatoryaffairs scientificreports gc word msds excel testing analysis regulatory toxicology microbiology registration communication ElectronicCommonTechnicalDocument RegulatorySubmissions AbbreviatedNewDrugApplication GenericProgramming2.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 Sanction
Your responsibilities include, but are not limited to:
Provide support to TA according to the needs for delivery activities, i.e. ICSR Medical review; co-authoring safety documents and a...
healthcareprofessionals musicmaking medicalreview riskmanagement medicalwriting computerskills problemsolving productquality drugdevelopment humanphysiology projectmanagement regulatoryaffairs presentationskills communicationskills internatiYour responsibilities include, but are not limited to: Provide support to TA according to the needs for delivery activities, i.e. ICSR Medical review; co-authoring safety documents and assisting in p...
healthcareprofessionals medicalreview riskmanagement medicalwriting productquality drugdevelopment humanphysiology projectmanagement regulatoryaffairs tatementsofworksowExp 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 RegulatoryRequirementsRole: Assistant Manager Regulatory Affairs (CMC) Location: Mumbai , BKC Reporting to: Head Regulatory An opportunity to work within the CMC Regulatory function of an established fast- moving and a...
verbalcommunication projectteams cosmetics drafting continuousimprovementfacilitation problemsolving legislativerelations lateralthinking documentation regulatoryaffairs greaterchina communicationskills talentmanagement medicaldevices envirotKeywords: Financial/ Regulatory Reporting, Regulatory Affairs,R2R. tLevel wise Experience:1. tOperations Manager Post CA 10 yearsu2019 Experience (excluding Article ship)Process Improvements , Change...
recordtoreport teamhandling generalledger changemanagement peoplemanagement regulatoryaffairs regulatoryreporting gl r2r rtr ledger taxation reporting management regulatory communication FA ProcessOrientation AOperationsRole: Assistant Manager Regulatory Affairs (CMC) Location: Mumbai , BKC Reporting to: Head Regulatory An opportunity to work within the CMC Regulatory function of an established fast- moving and a...
verbalcommunication projectteams cosmetics drafting continuousimprovementfacilitation problemsolving legislativerelations lateralthinking documentation regulatoryaffairs greaterchina communicationskills talentmanagement medicaldevices enviroDear Candidate, Greetings for the day! We are hiring forRegulatory Affairs Roles and Responsibilities:
Role: Assistant Manager Regulatory Affairs (CMC) Location: Mumbai , BKC Reporting to: Head Regulatory An opportunity to work within the CMC Regulatory function of an established fast- moving and a...
verbalcommunication projectteams cosmetics drafting continuousimprovementfacilitation problemsolving legislativerelations lateralthinking documentation regulatoryaffairs greaterchina communicationskills talentmanagement medicaldevices enviroShould be a B.Pharm / M.Pharm with Minimum 1 to 4 years of experience in QA / RA. Should have good communication skills. Should have experience in Pharma Industry. Should have experience in Quality As...
inspection iso iso9001standards microsoftword ctd qualityassurance regulatoryaffairs qa email pharma assurance regulatory communication GxP ChangeControl QualityAuditing Corrective PreventiveAction ComputerSystemValidation SoftwareQualiJob Title: Regulatory Affairs (Labeling) - US Market Company: Leading Pharmaceutical company. Designation: Reviewer No. of Positions: 6 Division: R&D (OSD) Department: Regulatory A...
globalteams changemanagement regulatoryaffairs packagingdevelopment set reach pharma planning clinical packaging management commercial consulting compliance regulatory maintenance regulations preparation availability lobalCrossFunctionaJob Title: Regulatory Affairs (Biologics) Company: Leading BioPharma Company in Bangalore Location (USFDA Approved) Designation: Associate Director Reporting to: Head of Regulatory ...
continuousimprovementfacilitation duediligence strategycreation regulatoryaffairs clinicaldevelopment productmanufacturing emotionalintelligence cmc ich ema cgmp email usfda pharma salary medical biology trategThe Medical Education Specialist will support medical education activities for both external and internal customers. This position directly reports to the Head Medical Education. Key Relationships: ...
marketingcrmsalesusinessdevelopmentmedicaldevicescustomerfocustrainingprogramseducationaltrainingclienthandlingtechnicalsupporttrainingneedsmedicaleducationregulatoryaffairshealthcareindustryPerform 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...
streamschemistryindpharmaceuticsvizpharmacognosyassurancepharmacologyregulatoryschedulemcregulatoryaffairsregulatorysubmissionsqualityassuranceregulatoryaffairscommontechnicaldocumentgenericprogrammingabbreviatednewdrugapplicationelectron1. 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...
streamschemistryindpharmaceuticsvizpharmacognosyassurancepharmacologyregulatoryschedulemcregulatoryaffairsregulatorysubmissionsqualityassuranceregulatoryaffairscommontechnicaldocumentgenericprogrammingabbreviatednewdrugapplicationelectronDesired Profile Dossier compilation & submissions for pharmaceutical product in Asian/ African Countries as per plan. Review of query and to ensure timely response to queries from Regulatory Agency. F...
gmpqmsevaluationstpvalidationcompilationdmfeducationgencydatacollectionlifecyclefillingclinicalprocessvalidationregulatoryaffairsregulatoryproductlifecyclesmfcompensationDesired Profile Dossier compilation & submissions for pharmaceutical product in Asian/ African Countries as per plan. Review of query and to ensure timely response to queries from Regulatory Agency. F...
gmpvalidationevaluationqmsdmfstpeducationcompilationroductlifecycleagencycompensationregulatoryaffairsregulatorylifecycleprocessvalidationsmfdatacollectionclinicalfillingDesired Profile Dossier compilation & submissions for pharmaceutical product in Asian/ African Countries as per plan. Review of query and to ensure timely response to queries from Regulatory Agency. F...
gmpqmsevaluationstpvalidationcompilationdmfeducationgencydatacollectionlifecyclefillingclinicalprocessvalidationregulatoryaffairsregulatoryproductlifecyclesmfcompensationDesired Profile Dossier compilation & submissions for pharmaceutical product in Asian/ African Countries as per plan. Review of query and to ensure timely response to queries from Regulatory Agency. F...
gmpvalidationevaluationqmsdmfstpeducationcompilationroductlifecycleagencycompensationregulatoryaffairsregulatorylifecycleprocessvalidationsmfdatacollectionclinicalfillingGreetings.!!! We, Sarthee Consultancy, are having opening in DRA department , for our client in Pharmaceutical Industry Please find details below Company :Leading name in Pharmaceutical Industry De...
drarugregulatoryaffairsregulatorydossierregulatoryaffairsWE HAVE URGENT OPENING FORRA EXECUTIVE Post: RA EXECUTIVE Job Location:MUMBAI No. of Requirements:06 Required Qualification: B.pharma /M.phbarma /D.pharma Salary:Salary will be deci...
compilationechnicaldocuments.dossiersrowactdregulatoryaffairsregulatorycompliancemanagementctdpreparationhealthcareregulatoryreportinglegaldocumentsa.Develops and initiates standards and methods for inspection, testing, and evaluation of the products b.Establishes program to evaluate precision and accuracy of production equipment an...
fdadaregulationsmethodsforinspectionevaluationoftheproductsqcmanagerisotestingproperdocumentationofqualityregulatoryaffairsfdaapprovedmaintainingofbmrrecords© 2019 Hireejobs All Rights Reserved