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To compile, review, and submit dossiers to different Regulatory Bodies (i.e. ASIAN, AFRICAN, ANVISA, LATAM, EU, USother Regulatory as well as non regulated bodies) Needs: knowledge of CTD and ACTD...
certified tips trainerlife cyclesample preparationdossier preparationtechnical requirementsprofessional liabilityctdlatamanvisaartworkpackingmarketingregulatorypreparationServSafe InstructionTIPS Certi* OUR COMPANY At Boehringer Ingelheim we develop breakthrough therapies that improve the lives of both humans and animals. Founded in 1885 and family-owned ever since, Boehringer Ingelheim ta...
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certified tips trainerlife cyclesample preparationdossier preparationtechnical requirementsprofessional liabilityctdlatamanvisaartworkpackingmarketingregulatorypreparationServSafe InstructionTIPS CertiThe requirement for Assistant Manager QC Analytical Development & Drug Regulatory Affairs for Pharmaceutical Industry Job Responsibility
To compile, review, and submit dossiers to different Regulatory Bodies (i.e. ASIAN, AFRICAN, ANVISA, LATAM, EU, USother Regulatory as well as non regulated bodies) Needs: knowledge of CTD and ACTD...
certified tips trainerlife cyclesample preparationdossier preparationtechnical requirementsprofessional liabilityctdlatamanvisaartworkpackingmarketingregulatorypreparationServSafe InstructionTIPS CertiROLE SUMMARY Delivery of electronic and paper regulatory transactions in support of New Product Launches, Legalizations, and License maintenance (eg, COPP , GMP , FSC certifications etc) Cont...
change managementregulatory affairsdocument managementlegislative relationsregulatory submissionsgmpsoftwareplanninglaunchesreportingmanagementcomplianceregulatorymonitoringJob Details
SALARY: up to 4 Lakhs LOCATION : Hyderabad, Telangana, India VACANCIES: 1 QUALIFICATION...
regulatorymarketingpermissionsrecruitmentavailabilityrecordssoundnocplacementfacilitiespharmaplanningmedicinedocumentationcontinuous improvement facilitationpreparationcommunication skillsagencymedicalfdaTo compile, review, and submit dossiers to different Regulatory Bodies (i.e. ASIAN, AFRICAN, ANVISA, LATAM, EU, USother Regulatory as well as non regulated bodies) Needs: knowledge of CTD and ACTD...
certified tips trainerlife cyclesample preparationdossier preparationtechnical requirementsprofessional liabilityctdlatamanvisaartworkpackingmarketingregulatorypreparationServSafe InstructionTIPS CertiCandidates with 3 - 5 years experience in liasoning with FDA for Manufacturing License and processing COPP ,FSC, MMC applications & uploading on Sugam portal. Purchase Pharmaceutical Packaging Ma...
continuous improvement facilitationregulatory affairsmaterial procurementpharmaceutical packagingfdammcpharmapackaginglicensingliasoningregulatoryprocurementContinuous Improvement CultureKaizenRoot Cause AnalysisSix SigmaLean Manufacturmin. 1 - 4 years of same area Salary As per industry norms. Job responsibilities : 1) Should have sound knowledge of FDA documentation (Domestic and Exports). 2) Should have multi-tasking attribu...
marketingdocumentationplanningcommunication skillsExecutive / Sr. Executive - Regulatory Affairs Desired Eligibility Pharma. Graduate and / or Post - Graduate in Science Minimum 2 4 years relevant experience. As per industry norms. Job responsibili...
regulatory affairsctdichscienceregulatorypreparationeligibilityregistrationElectronic Common Technical DocumentRegulatory SubmissionsAbbreviated New Drug ApplicationGeneric ProgrammingCMC Regulatory AffairsComJob Title : Mineral Chemist Job Code : MC01 Date of Posting : 14 / 05 / 2018 Profile : Minerals Laboratory Qualification : MSc(Chemistry) Experience : 3 - 5 Years Send Resume to : hr.sta...
resumemineralsCertified Professional Resume WriterExecutive BiosVideo ResumesProfessional BiosEmployee Referral ProgramsBoolean SearchingCareer ChangersBase MetalsNickelCoppStrong Interest InventDicecomCandidates with 3 - 5 years experience in liasoning with FDA for Manufacturing License and processing COPP ,FSC, MMC applications & uploading on Sugam portal. Purchase Pharmaceutical Packaging Ma...
continuous improvement facilitationregulatory affairs material procurementpharmaceutical packaging fdammc pharmapackagingTo compile, review, and submit dossiers to different Regulatory Bodies (i.e. ASIAN, AFRICAN, ANVISA, LATAM, EU, USother Regulatory as well as non regulated bodies) Needs: knowledge of CTD and ACTD...
certifiedtipstrainer lifecycle samplepreparation dossierpreparation technicalrequirements professionalliability eu ctd latam anvisa artwork packing marketing regulatory preparation ServSafeInstruction IPSCertiJob Title : Mineral Chemist Job Code : MC01 Date of Posting : 14 / 05 / 2018 Profile : Minerals Laboratory Qualification : MSc(Chemistry) Experience : 3 - 5 Years Send Resume to : hr.sta...
resume minerals CertifiedProfessionalResumeWriter ExecutiveBios VideoResumes ProfessionalBios EmployeeReferralPrograms BooleanSearching CareerChangers BaseMetals Nickel Copp trongInterestInvent Dicecommin. 1 - 4 years of same area Salary As per industry norms. Job responsibilities : 1) Should have sound knowledge of FDA documentation (Domestic and Exports). 2) Should have multi-tasking attribu...
marketing documentation planning ommunicationskillsCandidates with 3 - 5 years experience in liasoning with FDA for Manufacturing License and processing COPP ,FSC, MMC applications & uploading on Sugam portal. Purchase Pharmaceutical Packaging Ma...
continuous improvement facilitationregulatory affairs material procurementpharmaceutical packaging fdammc pharmapackagingROLE SUMMARY Delivery of electronic and paper regulatory transactions in support of New Product Launches, Legalizations, and License maintenance (eg, COPP , GMP , FSC certifications etc) Continuous Im...
rainee Executive License maintenance legalizations Legal Supp Product License SuppJob responsibilities : 1) Should have sound knowledge of FDA documentation (Domestic and Exports). 2) Should have multi-tasking attributes and should have excellent communication skills to interact ...
marketing pharma xecutive knowledgeoffdadocumentationViewsimilarjobsJob responsibilities : 1) Should have sound knowledge of FDA documentation (Domestic and Exports). 2) Should have multi-tasking attributes and should have excellent communication skills to interact ...
pharma marketing xecutive knowledgeoffdadocumentationViewsimilarjobsTo compile, review, and submit dossiers to different Regulatory Bodies (i.e. ASIAN, AFRICAN, ANVISA, LATAM, EU, USother Regulatory as well as non regulated bodies) Needs: knowledge of CTD and ACTD...
certifiedtipstrainer lifecycle samplepreparation dossierpreparation technicalrequirements professionalliability eu ctd latam anvisa artwork packing marketing regulatory preparation ServSafeInstruction IPSCertiExecutive / Sr. Executive - Regulatory Affairs Desired Eligibility Pharma. Graduate and / or Post - Graduate in Science Minimum 2 4 years relevant experience. As per industry norms. Job responsibili...
regulatory affairsctd ichscience regulatorypreparation eligibilityregistration Electronmin. 1 - 4 years of same area Salary As per industry norms. Job responsibilities : 1) Should have sound knowledge of FDA documentation (Domestic and Exports). 2) Should have multi-tasking attribu...
marketing documentation planning ommunicationskillsUrgent opening in pharmaceutical industry - (Delhi) Designation: Executive-Drug Regulatory Affairs Qualification: B.Pharma Experience: Minimum 2 years Job Location: Delhi Salary: 4 LPA 1. RA tea...
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Executive / Senior Executive DRA -ROW Markets
ROLE SUMMARY Delivery of electronic and paper regulatory transactions in support of New Product Launches, Legalizations, and License maintenance (eg, COPP , GMP , FSC certifications etc) Continuous Im...
rainee Executive License maintenance legalizations Legal Supp Product License SuppJob Title : Mineral Chemist Job Code : MC01 Date of Posting : 14 / 05 / 2018 Profile : Minerals Laboratory Qualification : MSc(Chemistry) Experience : 3 - 5 Years Send Resume to : hr.sta...
resume minerals CertifiedProfessionalResumeWriter ExecutiveBios VideoResumes ProfessionalBios EmployeeReferralPrograms BooleanSearching CareerChangers BaseMetals Nickel Copp trongInterestInvent DicecomURGENT REQUIREMENT FOR QUALIFIED AND EXPERIENCED REGULATORY AFFAIRS SPECIALIST FOR FAST GROWING, FINISHED FORMULATIONS CO. QUALIFIED CANDIDATES WITH RELEVANT EXPERIENCE IN REGULATORY AFFAIRS FOR SEMI...
pharma egulatoryaffairsJOB PURPOSE
ROLE SUMMARY Delivery of electronic and paper regulatory transactions in support of New Product Launches, Legalizations, and License maintenance (eg, COPP , GMP , FSC certifications etc) Continuous Im...
rainee ExecutiveLicense maintenancelegalizationsLegal SuppProduct License SuppDear ALL, We have Urgent Vacancy for QA MANAGER in boisar location. Company will be API PLANT USFDA APPROVED. Experience - 7 to 20 Yrs Designation - SR.EXECUTIVE / MANAGER CTC Range - 7 TO 14 Lac...
bprgmpbomcomsopoosqmsapiisoaptootsmfbmrJob Details : HR Executive ( Pharma Company) To maintain Attendance, Leave & other statutory registers/ Records. To Recruit manpower as per requirement. To prepare KRA of the employees To co-or...
payrollcommunicationrecruitmentwelfareacquisitionmployeeengagementtalentbenefitshumaninternalheadhuntingresourcecompensationDear All, We have vacancy for QA EXECUTIVE / Manager in Boisar Location . Company will be Pharma API PLANT USFDA APPROVED Qualification - B.sc/ M.sc Experience Required - 5 to 18 Years Package Ra...
1. RA team handling 2. Dossiers / Documents review 3. Guidelines of different regulatory authority updation to team. 4. Arranging documents from plant 5. Liasioning with plant QA / QC / Production...
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