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Roles and Responsibilities Shall operate the utility equipments (Air compressor, chiller, boiler, HVAC and water system) as per SOP instructions and enter the parameters which indica...
breakdown maintenancepreventive maintenanceenvironmental monitoringbmsisosophvaccapawaterpharmasparesalarmsscalesenglishinventoryequipmentprotocolsstatutoryemsPRODUCTION SHIFT INCHARGE (PHARMA API ONLY) Saurav Chemicals Limited (a USFDA Approved API manufacturing Pharmaceutical company is conducting interviews in PRODUCTION EXECUTIVE experience in pharma A...
production planningsafetyqualitygmpdocumentationcontinuous improvement facilitationlife sciencesapi manufacturingproduct developmentconducting interviewsapiusfdapharmaclinicalconductingmaintenanceContinuous Improvement CultureKaizenRootJob Title: Lead IT Operations and Compliance Qualification: B. Tech(CS)/B.E./BCA/Graduate + Computer Application Diploma with minimum 5+ years of working experience...
it operationsdata securityit compliancedata integritytraining needsquality controluser managementcustomer servicetechnical skillsteam developmentcapacity planningJob Title: Lead IT Operations and Compliance Qualification: B. Tech(CS)/B.E./BCA/Graduate + Computer Application Diploma with minimum 5+ years of working experience...
it operationsdata securityit compliancedata integritytraining needsquality controluser managementcustomer servicetechnical skillsteam developmentcapacity planningRoles and Responsibilities Candidate will be responsible for handling Quality Control of formulation based at Bangalore. You will be responsible for, 1. Candidate should have expe...
man managementquality controlosdmanedqmusfdapharmasupplycontrolequipmentmanagementregulatoryformulationMan PowerCPC NationalProfit Center ManagementMethod StatementsCOSHHHGVFootball CoachingRoles and Responsibilities Education : B.Pharma/ M.Pharma Exp required: 4-6 years Rich experience in packaging development as per USFDA requirement for solid oral pharmaceutical formu...
packaging machinespackaging developmentregulatory requirementspharmaceutical packagingusfdaartworkpackagingsuppliersregulatoryCorrugatedFolding CartonsFlexoFood PackagingPackaging EngineeringRetail PackagingLabelsArtiosCADDie CuttingElecRoles and Responsibilities 1) Computerized System Validation (CSV) Associate or Analyst Job Profile: The responsibilities will include developing validation documentation and support ...
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Roles and Responsibilities
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He should be aware with cGMP, ICH Q7, USFDA, WHO-GMP guidelines. To carry-out sampling and analysis Finished Goods and Raw material as per Quality Plan. Maintain records of analysis, allocation of f...
documentationhplcquality controlquality assurance(10+2 with relevant experience for Plant operator/technician) SALARY 200000 TO 300000 Desired Candidate Profile. Dear candidates,Saurav Chemicals Limited (a USFDA App...
safetypumpscommissioningplcshutdowncontinuous improvement facilitationclinical researchapi manufacturingproduct developmentapiusfdapharmaresearchclinicalmaintenanceContinuous Improvement CultureKaizenRoot Cause AnalysisSix SigmaAssoc Eng, Eng Services - LMC Apply Now Save Job This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, y...
pilot projectsconductivity metercgmpsop preparationrpmservice contractmhrawaterph meterhigh pressuretemperature gaugecqachange controlinstrument calibrationsopcfm(10+2 with relevant experience for Plant operator/technician) SALARY 200000 TO 300000 Desired Candidate Profile. Dear candidates,Saurav Chemicals Limited (a USFDA App...
safetypumpscommissioningplcshutdowncontinuous improvement facilitationclinical researchapi manufacturingproduct developmentapiusfdapharmaresearchclinicalmaintenanceContinuous Improvement CultureKaizenRoot Cause AnalysisSix SigmaPRODUCTION SHIFT INCHARGE (PHARMA API ONLY) Saurav Chemicals Limited (a USFDA Approved API manufacturing Pharmaceutical company is conducting interviews in PRODUCTION EXECUTIVE exper...
production planningsafetyqualitygmpdocumentationcontinuous improvement facilitationclinical researchapi manufacturingproduct developmentconducting interviewsapiusfdapharmaresearchclinicalconductingmaintenanceContinuous Improvement CultureTo perform analytical method validation / Verification / Method transferfor drug substances and injectable drug products within given timelines.
Designation: Assistant Manager IT Operations and Compliance Job Location: Bangalore Department: Information Technology About Syngene Incorporated in 1993, Syngen...
continuous improvement facilitationmisaccounts21 cfrequal employment opportunityaudit trailtatanimal healthit operationssalesdata securityph meterbankingmusic makingTo perform analytical method validation / Verification / Method transferfor drug substances and injectable drug products within given timelines.
EY- GDS Consulting Enterprise Risk (ER) Regulatory Compliance Senior As part of our EY-ER- Regulatory Compliance team, you will help the clients b...
quality auditrisk analysislife cyclesoftware quality assurance21 cfrbusiness process transformationfortune 500test scriptsclient focusservice linescomputer system validationmusic makingit riskDesignation: Executive Job Location: Bangalore Department: GLP-Analytical About Syngene Incorporated in 1993, Syngene Internation...
safety practicescontinuous improvement facilitationstandard operating proceduresanimal healthmethod developmentanalytical equipmentph meterconsumer goodsms officeDesignation: Executive Job Location: Bangalore Department: GLP-Analytical About Syngene Incorporated in 1993, Syngene Internation...
safety practicescontinuous improvement facilitationstandard operating proceduresanimal healthmethod developmentanalytical equipmentph meterconsumer goodsms officeDesignation: Executive Job Location: Bangalore Department: GLP-Analytical About Syngene Incorporated in 1993, Syngene Internation...
safety practicescontinuous improvement facilitationstandard operating proceduresanimal healthmethod developmentanalytical equipmentph meterconsumer goodsms officeDesignation: Executive Job Location: Bangalore Department: GLP-Analytical About Syngene Incorporated in 1993, Syngene Internation...
safety practicescontinuous improvement facilitationstandard operating proceduresanimal healthmethod developmentanalytical equipmentph meterconsumer goodsms officeDesignation: Executive Job Location: Bangalore Department: GLP-Analytical About Syngene Incorporated in 1993, Syngene Internation...
safety practicescontinuous improvement facilitationstandard operating proceduresanimal healthmethod developmentanalytical equipmentph meterconsumer goodsms officeDesignation: Executive Job Location: Bangalore Department: GLP-Analytical About Syngene Incorporated in 1993, Syngene Internation...
safety practicescontinuous improvement facilitationstandard operating proceduresanimal healthmethod developmentanalytical equipmentph meterconsumer goodsms officeDesignation: Executive Job Location: Bangalore Department: GLP-Analytical About Syngene Incorporated in 1993, Syngene Internation...
safety practicescontinuous improvement facilitationstandard operating proceduresanimal healthmethod developmentanalytical equipmentph meterconsumer goodsms officeplant head in delhiShould have a charming, positive and problem-solving attitude* Should ensure healthy inter-personal communication with various departments and senior management.* Should believe in ...
problem solvingisoquality controlmonthly reportsdeliverycontinuous improvement facilitationquality management systemqualityprocess controlPosition Summary: We are seeking a highly motivated Sr. Research Associate with hands-on experience in Ligand Binding Assay (LBA) development. The individual will join the Global Bioanalytica...
electronic data managementhplcdocumentationvalidationanalytical chemistrycalibrationdata managementligand bindingresearchquality assurancemethod validationmethod developmentprotein chemistryliquid handling* JOB OVERVIEW: A versatile and resourceful engineering project manager with Specialization in Oral solid dosage form equipment + HVAC KEY STAKEHOLDERS: INTERNAL Production, Finance, Supply Chai...
marketingsalesfinanceaccountsproject engineering managementsupply chainnew projectsequipment supplyenergy conservationregulatory agenciesoperational excellenceapi 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 cosmeticsRoles and Responsibilities 1) Computerized System Validation (CSV) Associate or Analyst Job Profile: The responsibilities will include developing validation documentation and support ...
21 cfrwritingcontinuous improvement facilitationequipment validationprocess automationglpgcpwriting skillscfrgampcomputerized systemsgmpusfdatechnical writingcomputerized system validationlaboratory automationstatements of work sow Department:Regulatory Affairs
Designation:Executive/Sr.Executive
Industry:Pharma/API
Experience: 3 to 7 years(Mandatory)
Roles and Responsibilities 1) Computerized System Validation (CSV) Associate or Analyst Job Profile: The responsibilities will include developing validation documentation and support ...
21 cfrwritingcontinuous improvement facilitationequipment validationprocess automationglpgcpwriting skillscfrgampcomputerized systemsgmpusfdatechnical writingcomputerized system validationlaboratory automationstatements of work sow: Rich experience in packaging development as per USFDA requirement for pharmaceutical formulations, setting of specifications and sourcing. Should possess thorough knowledge on pharmaceutical packagi...
packaging machinespackaging developmentpharmaceutical packagingusfdapackagingspecificationsFolding CartonsFlexoFood PackagingPackaging EngineeringRetail PackagingLabelsArtiosCADartwregulatrugatedCapabilities: Rich experience in packaging development as per USFDA requirement for pharmaceutical formulations, setting of specifications and sourcing. Should possess thorough kno...
packaging machinespackaging developmentpharmaceutical packagingusfdapackagingspecificationsFolding CartonsFlexoFood PackagingPackaging EngineeringRetail PackagingLabelsArtiosCADartwregulatrugatedCapabilities: 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...
analytical method developmentregulatorymhraftirusfdatgainstrumentsanvisadissolutionmccvalidationstability studieshplcregulatory auditsanalyticalmethod developmentvariance analysisoperationsfdaJob Description and responsibilities; - Capabilities: Rich experience in packaging development as per USFDA requirement for pharmaceutical formulations, setting of specifications and sourcing. Shoul...
researchhplcchemistryvalidationapipackaging machinespackaging developmentpharmaceutical packagingusfdapackagingspecificationsFolding CartonsFlexoregulaty requirementsartwregulatrugatedFood PackaCapabilities: Rich experience in packaging development as per USFDA requirement for pharmaceutical formulations, setting of specifications and sourcing. Should possess thorough knowledge on pharmaceut...
researchhplcchemistryvalidationapipackaging machinespackaging developmentpharmaceutical packagingusfdapackagingspecificationsFolding CartonsFlexoFood PackagingartwregulatrugatedPackaging Engineeriintern_regulatory management in chennai * **Master level of education in pharmacy or life sciences with a strong emphasis in chemistry or biology,**...
ms officelife sciencesrimsexcelveevavaultusfdabiologyenglishsoftwareeducationchemistrymaterialsmanagementpowerpointregulatoryexcipientsfdamedicalEY- GDS Consulting Enterprise Risk (ER) Regulatory Compliance Senior As part of our EY-ER- Regulatory Compliance team, you will help the clients by understanding their business needs...
test scriptsfortune 500business process transformationenvironmental impact assessment21 cfrsoftware quality assuranceclient focusit riskcomputer system validationlife cycleRoles and Responsibilities : * Comprehensive understanding of complete validation life cycle, risk based qualification methodology
Roles and Responsibilities : * Comprehensive understanding of complete validation life cycle, risk based qualification methodology
Roles and Responsibilities : * Comprehensive understanding of complete validation life cycle, risk based qualification methodology
Designation: Formulation Development Senior Research Associate Job Location: Bangalore Department: Pharmaceutical Development About Syngene Incorporated in 1993, Syngene International Ltd. is an i...
stability studiesvalidationcontinuous improvement facilitationbatch recordsliteratureliquid oralsnmrconsumer goodsresearchequal employment opportunityanimal healthhplcRoles and Responsibilities
Designation: Formulation Development Senior Research Associate Job Location: Bangalore Department: Pharmaceutical Development About Syngene Incorporated in 1993, Syngene International Ltd. is an i...
stability studiesvalidationcontinuous improvement facilitationbatch recordsliteratureliquid oralsnmrconsumer goodsresearchequal employment opportunityanimal healthhplcGreetings from Unichem Labs Ltd! We are looking for qualified and experienced candidates for our facility based at Ghaziabad, Uttar Pradesh (USFDA approved). Ca...
quality controlclinical researcherpbscsoptgalimsmhrausfdapharmacontrolresearchclinicalinstrumentscommunicationRadiographic TestingNDEUS PharmacopeiaEY- GDS Consulting Enterprise Risk (ER) Regulatory Compliance Staff As part of our EY-ER- Regulatory Compliance team, you will help the clients by understanding their business needs...
business process transformationenvironmental impact assessmentcomputer system validationsoftware quality assuranceit risk21 cfrstatements of work sow
EY- GDS Consulting Enterprise Risk (ER) Regulatory Compliance Manager As part of our EY-ER- Regulatory Compliance team, you will help the clients by understanding their business need...
business process transformationclient focuslife cyclefortune 500test scriptsenvironmental impact assessmentsoftware quality assurance21 cfrcomputer system validationit risk© 2020 Skillindia All Rights Reserved