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Exp: 8+ Job Title CoNQ Project Manager Implement and drive a company-wide program to ensure products meet Cost-of-Non-Quality meets targets in close collaboration with cross functional teams. Moreove...
continuous improvement facilitationiso 13485problem solvingmedical device directivemedical devicesleadership skillssupplier quality21 cfrchange ordersIndustry - Medical / Healthcare / Hospital Category - Consulting Skills - AI Medical Imaging Job Type - Permanent - Work as a global manager for RA and QA for AI software(Medical Imaging) - Get gr...
iso 14971design control21 cfrregulatory intelligenceworking experienceiso 13485At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Job Overview detail designdesign controlmedical devicesrisk assessmenttechnical skillsproduct managementquality managementdesign developmentdevice developmentmedical technologyproduct developmentfeasibility studies
Who we want:
Who we want:
Who we want:
Exp: 8+ Job Title CoNQ Project Manager Job Description In this role; you have the opportunity to Implement and drive a company-wide program to ensure products meet Cost-of-Non-Quality meets targets i...
leadership skillsmedical device directive21 cfrproblem solvingchange ordersmedical devicessupplier qualityiso 13485Exp: 8+ Job Title CoNQ Project Manager Implement and drive a company-wide program to ensure products meet Cost-of-Non-Quality meets targets in close collaboration with cross functional teams. Moreove...
continuous improvement facilitationiso 13485problem solvingmedical device directivemedical devicesleadership skillssupplier quality21 cfrchange ordersAt TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Job Overview detail designdesign controlmedical devicesrisk assessmenttechnical skillsproduct managementquality managementdesign developmentdevice developmentmedical technologyproduct developmentfeasibility studies
Exp: 8+ Job Title CoNQ Project Manager Job Description In this role; you have the opportunity to Implement and drive a company-wide program to ensure products meet Cost-of-Non-Quality meets targets i...
leadership skillsmedical device directive21 cfrproblem solvingchange ordersmedical devicessupplier qualityiso 13485null #LI-PHILIN Job Description Job Title - Customer Advocate - Complaint Specialist Job Location - Pune Chakan KEY ARE...
adverse event reportingmedical devicesiso 13485iso 14971post market surveillancerisk assessmentmedical device directive21 cfrfield servicerisk managementcontinuous improvement facilitationinternal auditAt Cepheid, we are passionate about improving healthcare through faster, more accurate diagnostic tests. With our GeneXpert System, we ve taken the most sophisticated molecular technology and packaged...
test case designtest scenariosenvironmentiso 13485in vitrocenter of excellencetest executionin vitro diagnosticsdanaher business systemtest casesstatements of work sowresearch developmentglobal rdSENIOR DESIGN QUALITY ENGINEER Careers that Change Lives Help streamline and speed our time to market and build quality in at every step. You will be a member of the new product dev...
inspectionqualityquality controlisocalibrationnew product developmentstatistical data analysisverificationvalidationquality management systemstatements of work sowImmediate hiring for Cyber Security Exp: 5 to 10 Years Job Location : Bangalore / Chennai / Hyderabad / Pune EXPERIENCE AND REQUIRED SKILLS:
null In this role, you have the opportunity to In this role, you can run projects as a part of Global Procurement Team and have a visible impact on finding the best way to meet the ...
reliabilityfmeamechanicalsafetycommissioningcorrectivepreventive actionroot cause analysisnew product developmentmedical device directiveservice center operationssupplier quality engineeringRequirements:
Exp: 8+ Job Title CoNQ Project Manager Implement and drive a company-wide program to ensure products meet Cost-of-Non-Quality meets targets in close collaboration with cross functional teams. Moreove...
continuous improvement facilitationiso 13485problem solvingmedical device directivemedical devicesleadership skillssupplier quality21 cfrchange ordersnull You will have the opportunity to Perform reliability testing for range of products and the components in such a way that all the realized products options and features; are ver...
root cause analysisnew product developmentmedical device directiveservice center operationssupplier quality engineeringreliabilitycorrectivepreventive actionJob Description Roles and Responsibilities: Primarily responsible for: Risk management, Risk Table creation & Analysis, FMEAs, Quality Plan, Literature Review, Device Master Record, Quality Trainin...
inspectioncalibrationrisk assessmentproduct qualityquality controlrisk managementcontinuous improvement facilitationdata analysisinternal auditRequirements:
Job Description
The R&D DA Lab Supervisor will be a part of the R&D quality organization and lead the Design Assurance (DA) Lab . The individual...
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Job Description
The R&D DA Lab Supervisor will be a part of the R&D quality organization and lead the Design Assurance (DA) Lab . The individual...
designassurance workinstructions projectmanagement qualitymanagement classii iso13485 fixturedesign riskmanagement iso14971 designcontrol testequipment projectmanagementtraining projectteams qualitystandards medicaldevices producttesting
Be responsible for establishing in approved documents, maintain and continuously improve Quality System processes required by international, regional and national regulatory authorities and standards ...
gapanalysis sow iso9001 iso14971 newproductdevelopment keyperformanceindicators qualitysystem qualitysystemimplementation postmarketsurveillance productdevelopment productdesign systemimplementation qa qualityengineering processvalidationJob Description
Production Officer
Location:Mumbai / Turbhe
Preferences:Job Description Roles and Responsibilities: Primarily responsible for: Risk management, Risk Table creation & Analysis, FMEAs, Quality Plan, Literature Review, Device Master Record, Quality Trainin...
inspection calibration iskassessment productquality qualitycontrol riskmanagement continuousimprovementfacilitation dataanalysis internalauditSQA - CMMi (Level 3) with exp in implementing CMMi level 3 process and to get the certification.To create quality plans & assurance of adherence, Definition of product software quality gates, Executio...
presentations adherence reviews cmmi sqa assurance gxp bsc metrics software so13485 iso14971 21cfr qualitysystems designcontrol correctivepreventiveaction verificationvalidation softwarequality
Manage an effective corrective and preventive action and drive the improvements of quality in the business. Manage, guide and lead quality team. Develop, manage and reports on KPIs PPAP activities...
qualitystandards cleaningvalidation deviations iso14971 codes analysis reliability trackwise business regulations ppap 21cfr lean preventiveaction continuousimprovement gxp preparation asepticprocessing orrectivepreventiveaction verificJob Description Roles and Responsibilities: Primarily responsible for: Risk management, Risk Table creation & Analysis, FMEAs, Quality Plan, Literature Review, Device Master Record, Quality Trainin...
inspection calibration iskassessment productquality qualitycontrol riskmanagement continuousimprovementfacilitation dataanalysis internalaudit1. Experience in preparing continental stuff also plan, implement food and culinary preparation activities. 2. Prepare and manage kitchen budget and always have to preserve food quality. 3. Give fin...
designcontrol gxp hotel benefits preparation menudevelopment designation finedining certifiedqualityauditor 21cfr plates continentalcuisine iso14971 changecontrol qsr erificationvalidation correctivepreventiveactionTitle Senior Research Associate Services Analytical Services Job Function Analytical Services Job Grade Senior Research Associate (GC) SBU/ Division GVK FAS Candidate Profile Qualification Exper...
cgmp gc hplc validation research nmr basic analysis literature calibration analytical orrectivepreventiveaction iso14971 methodvalidation verificationvalidation designc methoddevelopment qualitysystemsTitle Senior Research Associate (ICPMS) Services GVK FAS Job Function GVK FAS Job Grade Senior Research Associate (ICPMS) SBU/ Division Analytical R&D Candidate Profile Qualification Experience ...
hplc nmr literature basic analytical calibration validation cgmp analysis research esigncontr methoddevelopment methodvalidation verificationvalidation iso14971 qualitysystems correctivepreventiveactionThe successful candidate will be actively involved in the development and engagement of the overall team ensuring the quality delivery of the project for product development and Process development. T...
sales management mis customerrelations quality newproductdevelopment continuousimprovementfacilitation socialmedia dataanalysis internalaudit productsafety qualitysystem riskmanagement riskassessment productquality seniormanagement regulatTitle Senior Research Associate Services Analytical Services Job Function Analytical Services Job Grade Senior Research Associate (GC) SBU/ Division GVK FAS Candidate Profile Qualification Exper...
cgmp gc hplc validation research nmr basic analysis literature calibration analytical orrectivepreventiveaction iso14971 methodvalidation verificationvalidation designc methoddevelopment qualitysystemsMust have a work experience in IEC 60601-1 (and associated collateral standards) .The position will participate in the development of product specifications , ensuring project compliance to internal a...
design cmdcas risk marking iii fda medical iec iso egulatoryrequirements regulatorycompliance iso14971 iec60601 qualityengineering productdesign riskanalysis iso13485 productdevelopment cemarkingTitle Senior Research Associate Services Analytical Services Job Function Analytical Services Job Grade Senior Research Associate (GC) SBU/ Division GVK FAS Candidate Profile Qualification Exper...
cgmp gc hplc validation research nmr basic analysis literature calibration analytical orrectivepreventiveaction iso14971 methodvalidation verificationvalidation designc methoddevelopment qualitysystemsSQA - CMMi (Level 3) with exp in implementing CMMi level 3 process and to get the certification.To create quality plans & assurance of adherence, Definition of product software quality gates, Executio...
presentations adherence reviews cmmi sqa assurance gxp bsc metrics software so13485 iso14971 21cfr qualitysystems designcontrol correctivepreventiveaction verificationvalidation softwarequality*Considerable knowledge of the methods used to detect and correct hearing disorders. *Considerable knowledge of the pathology of hearing and speech disorders. *Ability to operate audiometric equipment...
healthcare throat equipment ent medical pathology disposables interpret otology edicaldevices iso13485 surgicalinstruments designcontrol iso14971 capitalequipment operatingroom sinussurgery medicalsales workingwithsurgeons earsurgery*Considerable knowledge of the methods used to detect and correct hearing disorders. *Considerable knowledge of the pathology of hearing and speech disorders. *Ability to operate audiometric equipment...
healthcare throat equipment ent medical pathology disposables interpret otology edicaldevices iso13485 surgicalinstruments designcontrol iso14971 capitalequipment operatingroom sinussurgery medicalsales workingwithsurgeons earsurgery*Considerable knowledge of the methods used to detect and correct hearing disorders. *Considerable knowledge of the pathology of hearing and speech disorders. *Ability to operate audiometric equipment...
healthcare throat equipment ent medical pathology disposables interpret otology edicaldevices iso13485 surgicalinstruments designcontrol iso14971 capitalequipment operatingroom sinussurgery medicalsales workingwithsurgeons earsurgeryJob Description Primarily responsible for: Risk Management, Design Inputs review, Design History File Documents review, Design Output Document review, Test log test plans, Software verification and ...
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