47 Quality Assurance And Engineering jobs in Bengaluru.

Bengaluru

• Skills: GST Operations, Safety Systems, Healthcare, Patient Care, Engineering, Medical Devices, Risk Management, Clinical Research, Supply Chain, Quality Assurance
• Type: Full time

Bengaluru

• Skills: Quality Assurance, Asset Integrity, Reliability Engineering, Robotics, Engineering, Consulting Services, Advanced NDE Inspections, Project Management, Continuous Improvement, Safety
• Experience: 7+ years of demonstrated supervisory experience within Oil & Gas or petrochemical industry
• Type: Full-time

Bengaluru

• Skills: clinical documents, writing, editing, QC review, regulatory guidelines, clinical study, document management, attention to detail, medical writing processes, MS/PhD
• Experience: 5+ years of experience as a medical writer in the sponsor and/or CRO setting

Bengaluru

• Skills: Engineering, Research and Development, Medical Devices, Innovation, Healthcare, Manufacturing, Compliance, Quality Systems, Patient Care, Technical Services
• Type: Full-time

Bengaluru

• Skills: Medical Writing, Biostatistics, Clinical Research, Content Creation, Regulatory Documentation, Clinical Trials, Pharmaceuticals, Data Management, Technical Writing, Compliance

Bengaluru

• Skills: software, verification, manager, engineering, research, development, medical, devices, healthcare, innovation
• Type: Full time

Bengaluru

• Skills: Software Verification, Engineering, Medical Devices, R&D, Product Security, Embedded Software, Electromechanical, Integration, Healthcare, Innovation
• Type: Full Time

Bengaluru

• Skills: study design, edit specifications, quality delivery, eCRF, EDC build components, Study Authorization Form, Internal Design Review Meeting, database design, LLRR data, Rights and Roles
• Type: Full time

Bengaluru

• Skills: Medical Writing, Safety Services, Project Management, Client Liaison, Performance Management, Signal Detection, Quality Control, Training, Collaborative Relationships, Regulatory Compliance

Bengaluru

• Skills: SAP PP, PPDS, Production Planning, Data Analysis, Functional Specifications, Testing, User Acceptance Testing, Mentoring, Medical Device Industry, Life Sciences
• Experience: Minimum 8 years of Implementing Production Planning and other related SAP modules is required.

Bengaluru

• Skills: clinical monitoring, monitoring visit reports, protocols, SOPs, compliance, action items, safety, study performance, ICH GCP, training
• Experience: Minimum 3 years experience in clinical monitoring, clinical trial management or equivalent

Bengaluru

• Skills: Quality Control, Biometrics, eCRFs, Data Management, Data Validation, ICH/GCP guidelines, clinical trial methodology, Medidata Rave EDC, SQL Server, Oracle
• Experience: Minimum 3-5 years in Pharmaceutical/Biotechnology industry or equivalent

Bengaluru

• Skills: Cyber Security, Quality Assurance, System Validation, Clinical Research, Data Management, Statistical Programming, Regulatory Compliance, Biostatistics, Project Management, Clinical Trials

Bengaluru

• Skills: Regulatory Affairs, Data Management, MDRiM, Data Quality, Compliance, MedTech, Medical Device, Process Improvement, Database Management, Cross-functional Environment
• Experience: 3+ years
• Type: Hybrid

Bengaluru

• Skills: design, electromechanical, robotics, medical products, mechanical components, failure analysis, design verification, manufacturing, risk assessments, regulatory compliance
• Experience: Minimum 8 years of experience designing and manufacturing electromechanical products

Bengaluru

• Skills: regulatory submissions, regulatory documentation, compliance, FDA, EMA, clinical trial, document management, regulatory guidelines, eCTD, submission processes
• Experience: 1-2 years

Bengaluru

• Skills: external data management, clinical data, local lab data, data transfer agreements, data quality, ICH/CGP compliance, data validation, vendor data processing, data transfer, data integrity
• Experience: 5+ years

Bengaluru

• Skills: regulatory strategies, medical device, FDA, EU MDR, global registrations, product submissions, ISO 13485, quality management system, regulatory compliance, post-market regulation
• Experience: 4+ years in medical device Regulatory Affairs

Bengaluru

• Skills: regulatory documents, FDA, EMA, regulatory submissions, document management, eCTD, clinical trial applications, regulatory guidelines, submission processes, system functionality
• Experience: 3 years in document management

Bengaluru

• Skills: quality audits, medical documentation, medical terminology, data labeling, clinical knowledge, HIPAA rules, quality assurance, collaboration, data annotation, medtech
• Experience: A minimum of 12 years’ experience in Medical Transcription or Medical Scribing required.

Bengaluru

• Skills: Quality, Regulatory, Complaints Management, Post-Market Surveillance, ISO 13485, Medical Devices, FDA, Customer Service, Troubleshooting, Risk Management
• Experience: 1-3 years in Medical Device industry or related field

Bengaluru

• Skills: Regulatory, Medical Devices, Global Regulatory Intelligence, EU MDR, clinical evaluation, Product claims, Regulatory submissions, EU Notified Body, Advertising and Promotion, Regulatory Trends
• Experience: 10+ years
• Type: Full-time

Bengaluru

• Skills: Manufacturing, PIs, Validation, Documents, MES, System Design, Process Design, Validation of PIs, Manufacturing Processes, Global PIs
• Type: Full-time

Bengaluru

• Skills: Clinical Data Management, Database Development, Quality Control, Data Management Documentation, Training, Clinical Trial, Medical Coding, CRF Specifications, Database Testing, Regulatory Compliance
• Experience: 5+ years’ Clinical Data Management experience
• Type: Full-time

Bengaluru

• Skills: supplier quality assurance, procurement quality control, engineering drawings, IQS software, quality-related target reports, supplier conformance, part qualification, collaboration, document verification, material test reports
• Experience: 2–4 years

Bengaluru

• Skills: Coding, MedDRA, WHODRUG, medical coding, quality control, clinical data, SOPs, training, documentation, data management
• Experience: 5+ years within Data Management
• Type: Full-time

Bengaluru

• Skills: Trial Master File, quality control, ICH-GCP, clinical trial, electronic TMF, data management, documentation, audit readiness, compliance, health reports
• Type: full_time
• Salary: {'min': None, 'max': None, 'period': '', 'currency': ''}

Bengaluru

• Skills: Quality Management System, medical device, supplier qualification, calibration logs, design controls, document control, regulatory audits, CAPA, training administration, electronic document management
• Type: full_time
• Salary: {'min': None, 'max': None, 'period': '', 'currency': ''}

Bengaluru

• Skills: Pharmacovigilance, Product Safety, Regulatory Compliance, GxP/GMP Compliance, Data Integrity, Change Management, Cross-Functional Leadership, CAPAs, Operational Management, IT Systems
• Type: full_time
• Salary: {'min': None, 'max': None, 'period': '', 'currency': ''}

Bengaluru

• Skills: Quality Assurance, ISO 9001:2015, Quality Management Systems, Lean Manufacturing, Technical Inspection Services, Manufacturing Quality, Project Standards Compliance, Incoming Quality Inspection, Materials Certification, Process Improvement
• Type: full_time
• Salary: {'min': None, 'max': None, 'period': '', 'currency': ''}