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Description: Handling IPQA Execution of Engg Related Filing , Reviewing the documents of ADL and QC (Analytical method validation protocol and reports, Audit trials, Routine QC sample analytical repor...
analyticalmethoddevelopment changecontrol methodtransfer methodvalidation methoddevelopment qc adl ipqa filing trials control protocol monit analytical validation preparation VarianceAnalysis egulat ing SecoCapabilities: Thorough understanding and on- hand experience in Analytical Method Development, Validation and Stability Studies as per EU/ US requirements. Having thorough knowledge of impurity profil...
analyticalmethoddevelopment regulatory mhra ftir usfda tga instruments anvisa dissolution mcc validation stabilitystudies hplc gc regulatoryaudits analytical methoddevelopment varianceanalysis operations daThorough understanding and on- hand experience in Analytical Method Development, Validation and Stability Studies as per EU/ US requirements. Having thorough knowledge of impurity profiling, dissoluti...
operations ethoddevelopment regulatoryaudits analyticalmethoddevelopmentRole :AR&D Expert Role Band :Blue No. of Positions : 1 Work Location : IPDO, Bachupally Key Responsibilities:
Capabilities: Thorough understanding and on- hand experience in Analytical Method Development, Validation and Stability Studies as per EU/ US requirements. Having thorough knowledge of impurity profil...
analyticalmethoddevelopment regulatory mhra ftir usfda tga instruments anvisa dissolution mcc validation stabilitystudies hplc gc regulatoryaudits analytical methoddevelopment varianceanalysis operations daThorough understanding and on- hand experience in Analytical Method Development, Validation and Stability Studies as per EU/ US requirements. Having thorough knowledge of impurity profiling, dissoluti...
operations ethoddevelopment regulatoryaudits analyticalmethoddevelopmentResearch Associate / Sr. Research Associate - Analytical R&D Research Associate / Sr. Research Associate M.Pharma / M.Sc. (Analytical Chemistry / Organic Chemistry) 3 - 5 years 1 - 2 years 0 - 1 years...
research validation hplc documentation calibration analyticalmethoddevelopment particlesize methodtransfer methoddevelopment dissolutionapparatus analyticalinstruments ir gc nalyticalrd regulat yguidelinesKnowledge of analytical method development, Validation and stability analysis of Oral and Injectable dosage forms. Handling of Tablets, Capsules, Oral Liquids and Oral Suspensions. Handling of dissolu...
research validation hplc documentation calibration analyticalmethoddevelopment particlesize methodtransfer methoddevelopment dissolutionapparatus analyticalinstruments ir gc uv glp egulat yguidelines stableResearch Associate / Sr. Research Associate - Analytical R&D Research Associate / Sr. Research Associate M.Pharma / M.Sc. (Analytical Chemistry / Organic Chemistry) 3 - 5 years 1 - 2 years 0 - 1 years...
research validation hplc documentation calibration analyticalmethoddevelopment particlesize methodtransfer methoddevelopment dissolutionapparatus analyticalinstruments ir gc nalyticalrd regulat yguidelinesLocation:Bengaluru Area , India Qualification: B. Pharma / M. Pharmacy / M.Sc. in organic chemistry / analytical chemistry 3 - 8 years of Experience in BA BE centre (CRO) / pharma is preferred. 1. O...
analyticalmethoddevelopment methoddevelopment analyticalchemistry lc glp icp sound pharma protocol matrices chemistry equipment operations compliance analytical validation milestones maintenance anicchemistry calibrDescription: Handling IPQA Execution of Engg Related Filing , Reviewing the documents of ADL and QC (Analytical method validation protocol and reports, Audit trials, Routine QC sample analytical repor...
analyticalmethoddevelopment changecontrol methodtransfer methodvalidation methoddevelopment qc adl ipqa filing trials control protocol monit analytical validation preparation VarianceAnalysis egulat ing SecoKnowledge of analytical method development, Validation and stability analysis of Oral and Injectable dosage forms. Handling of Tablets, Capsules, Oral Liquids and Oral Suspensions. Handling of dissolu...
research validation hplc documentation calibration analyticalmethoddevelopment particlesize methodtransfer methoddevelopment dissolutionapparatus analyticalinstruments ir gc uv glp egulat yguidelines stableResearch Associate / Sr. Research Associate - Analytical R&D Research Associate / Sr. Research Associate M.Pharma / M.Sc. (Analytical Chemistry / Organic Chemistry) 3 - 5 years 1 - 2 years 0 - 1 years...
research validation hplc documentation calibration analyticalmethoddevelopment particlesize methodtransfer methoddevelopment dissolutionapparatus analyticalinstruments ir gc nalyticalrd regulat yguidelinesQualification: 1.M.Sc Organic Chemistry / B. Pharma. / M. Pharma; 2 to 5 Years Job Profile 1.Experienced with good analytical hand in Analytical Method development / validation of finished product. 2...
analyticalmethoddevelopment methoddevelopment gc pharma chemistry analytical validation VarianceAnalysis SecondaryResearch FAR Essbase Economics Econometrics Hyperion Business anicchemistry FinancialF ecastingLocation:Bengaluru Area , India Qualification: B. Pharma / M. Pharmacy / M.Sc. in organic chemistry / analytical chemistry 3 - 8 years of Experience in BA BE centre (CRO) / pharma is preferred. 1. O...
analyticalmethoddevelopment methoddevelopment analyticalchemistry lc glp icp sound pharma protocol matrices chemistry equipment operations compliance analytical validation milestones maintenance anicchemistry calibrThorough understanding and on- hand experience in Analytical Method Development, Validation and Stability Studies as per EU/ US requirements. Having thorough knowledge of impurity profiling, dissoluti...
operations ethoddevelopment regulatoryaudits analyticalmethoddevelopment
Senior Scientist I Analytical Research and Development Tracking Code IND 161
Job Description This is a supervisory position in USP-India s Analytical Research & Development Laboratory. In ...
hplc validation api research documentation penaccess syntheticorganicchemistry analyticalmethodvalidation analyticalmethoddevelopment researchdevelopment wetchemistry standardoperatingprocedures iso9001Qualification: 1.M.Sc Organic Chemistry / B. Pharma. / M. Pharma; 2 to 5 Years Job Profile 1.Experienced with good analytical hand in Analytical Method development / validation of finished product. 2...
analyticalmethoddevelopment methoddevelopment gc pharma chemistry analytical validation VarianceAnalysis SecondaryResearch FAR Essbase Economics Econometrics Hyperion Business anicchemistry FinancialF ecasting
Senior Scientist I Analytical Research and Development Tracking Code IND 161
Job Description This is a supervisory position in USP-India s Analytical Research & Development Laboratory. In ...
hplc validation api research documentation penaccess syntheticorganicchemistry analyticalmethodvalidation analyticalmethoddevelopment researchdevelopment wetchemistry standardoperatingprocedures iso9001Scientist II - Analytical Research and Development Tracking Code IND 173 Job Description This is a non-supervisory position in USP-India s Analytical Research & Development Laboratory. In this role ,...
hplc api research calibration documentation echnicalwriting gcanalysis analyticalmethoddevelopment thermalanalysis researchdevelopment deliveringprojectsontime deliveryofprojects wetchemistry iso9001Scientist / Senior Associate Scientist|Navi Mumbai (Turbhe) |Pioneer Management Consultant Pvt Ltd AddThis Utility Frame Twitter Widget Iframe Mar 15th 2018 Key Skills : Analytical Method Development,...
marketing auditing research esearchdevelopment methodvalida problemsolving analyticalmethoddevelopment benefitsadministration continuousimprovementfacilitation analyticalskills qualitycontrol testprocedureshaving strong communication skills. having strong working hands with herbal care chemicals.
should have strong work exposure with hair herbal care product as chemistry Lab. Manage and prioritiz...
analyticalmethoddevelopment standardoperatingprocedures qualityaudit qualitycontrol computerskills microsoftoffice methoddevelopment analyticalchemistry maintenanceactivities it care tests herbal control heJob Title: Research Assocaite Department: Analytia research & development Division: Biologics/ Biosimilars Experience: 1- 5years Job Location: Bangalore Qualification: MscM.Sc. (Biochemistry, Mole...
analyticalmethoddevelopment ionexchange musicmaking reversephase dataintegrity datarecording sizeexclusion qualitysystems molecularbiology technicalreports proteinstructure methoddevelopment rocessdLocation:Bengaluru Area , India Qualification: B. Pharma / M. Pharmacy / M.Sc. in organic chemistry / analytical chemistry 3 - 8 years of Experience in BA BE centre (CRO) / pharma is preferred. 1. O...
analyticalmethoddevelopment methoddevelopment analyticalchemistry lc glp icp sound pharma protocol matrices chemistry equipment operations compliance analytical validation milestones maintenance anicchemistry calibrDear Analytical Professionals, Greetings!!! We are hiring for the below requirement AR&D - HPLC Method Development/ Validation / Routine Analysis - API Division : API Department :AR&D Qualific...
analyticalmethodvalidation analyticalmethoddevelopment musicmaking particlesize productanalysis methodvalidation finishedproducts methoddevelopment analyticalchemistry api hplc pharma ehavi altraining meDear Candidate, Greetings! Candidate should have experience in Pharma Respiratory, Inhalation.MDI,DPI,pulmonary. Holds credential Analytical method development, Analytical Method Validation, in Ana...
analyticalmethodvalidation analyticalmethoddevelopment productanalysis methodvalidation methoddevelopment cv dpi ctc pharma medical research analysis clinical healthcare analytical validation calibration ethodTranCURRENT OPENINGS Designation : ARD (Analytical Research & Development) Manager Designing, monitoring, interpreting & documenting analytical activities including method development, method validat...
analyticalmethoddevelopment methodvalidation stabilitystudies methoddevelopment it salary research openings protocols commercial monit analytical validation nalyticalrd regulat yguidelines regulat ing preparaKnowledge of analytical method development, Validation and stability analysis of Oral and Injectable dosage forms. Handling of Tablets, Capsules, Oral Liquids and Oral Suspensions. Handling of dissolu...
researchvalidationhplcdocumentationcalibrationanalyticalmethoddevelopmentparticlesizemethodtransfermethoddevelopmentdissolutionapparatusanalyticalinstrumentsglpegulatyguidelinesstableResearch Associate / Sr. Research Associate - Analytical R&D Research Associate / Sr. Research Associate M.Pharma / M.Sc. (Analytical Chemistry / Organic Chemistry) 3 - 5 years 1 - 2 years 0 - 1 years...
researchvalidationhplcdocumentationcalibrationanalyticalmethoddevelopmentparticlesizemethodtransfermethoddevelopmentdissolutionapparatusanalyticalinstrumentsnalyticalrdregulatyguidelines
Dear Candidate, Greetings! Candidate should have experience in Pharma Respiratory, Inhalation.MDI,DPI,pulmonary. Holds credential Analytical method development, Analytical Method Validation, in Ana...
analyticalmethodvalidationanalyticalmethoddevelopmentproductanalysismethodvalidationmethoddevelopmentdpictcpharmamedicalresearchanalysisclinicalhealthcareanalyticalvalidationcalibrationethodTranAnalysis and reviewing of documents like RM, FP, PM, Calibration report, validation report. Cross verification of inward register of raw material and retest raw material register and drug product. C...
pharmaceuticalsmhravalidationwhodocumentationusdfaooshplceviationanalyticalmethoddevelopmentuplcchangecontrolstabilitystudiesoosanvisaqmsqualityauditqualitycontrolAnalysis and reviewing of documents like RM, FP, PM, Calibration report, validation report. Cross verification of inward register of raw material and retest raw material register and drug product. C...
pharmaceuticalsmhravalidationwhodocumentationusdfaooshplceviationanalyticalmethoddevelopmentuplcchangecontrolstabilitystudiesoosanvisaqmsqualityauditqualitycontrolAnalysis and reviewing of documents like RM, FP, PM, Calibration report, validation report. Cross verification of inward register of raw material and retest raw material register and drug product. C...
pharmaceuticalsmhravalidationwhodocumentationusdfaooshplcdeviationanalyticalmethoddevelopmentuplcchangecontrolstabilitystudiesoosanvisaqmsqualityauditqualitycontrol© 2019 Hireejobs All Rights Reserved