Last updated: 2025-05-22

23 Quality Engineering jobs in Bengaluru.

Hiring now: Sr Engr Vv Flc @ Baxter, Sr External Data Spec @ Eclinical , Sr Regulatory Affairs Spe @ Alivecor, Gs Apac Regulatory Inform @ Johnson Jo, Associate Mgr Safety Medi @ Parexel, Quality Integrity Reliabi @ Chevron, Head Of Clinical Research @ Intuitive , Statistical Programmer Ii @ Alexion, Clinical Ops Spec @ Suki, Sr Medical Writer @ Precision .Explore more at at kaamvaam.com

🔥 Skills

Medical Devices (6) Risk Management (4) Project Management (4) Regulatory (3) FDA (3) EU MDR (3) Quality Control (3) Engineering (3) compliance (3) Quality (2)

📍 Locations

Bengaluru (23)

Baxter

Skills & Focus: Verification, Validation, Testing, Regulatory, Quality, Risk Management, Electro-mechanical, Reliability Engineering, Medical Devices, Test Automation
About the Company: Baxter's Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients needs globally. They have pi…
Experience: 5 to 10 yrs of experience in Verification and Validation testing
Benefits: Support for Parents, Continuing Education/ Professional Development, Employee Health & Well-Being, Paid Time Off, 2 Day…

Eclinical Solutions

Skills & Focus: 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
About the Company: eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate…
Experience: 5+ years

Alivecor

Skills & Focus: regulatory strategies, medical device, FDA, EU MDR, global registrations, product submissions, ISO 13485, quality management system, regulatory compliance, post-market regulation
About the Company: AliveCor imagines a healthier world powered by access to personalized intelligent information. Pioneers over-the-counter medical EKG devices, empowering consum…
Experience: 4+ years in medical device Regulatory Affairs
Benefits: Hybrid working model, flexible vacation, maternity/paternity leave, medical benefits, metro connectivity, collaborative…

Johnson & Johnson

Skills & Focus: Regulatory Affairs, Data Management, MDRiM, Data Quality, Compliance, MedTech, Medical Device, Process Improvement, Database Management, Cross-functional Environment
About the Company: Johnson & Johnson is a global healthcare company that focuses on innovative medicine and medical technology, creating solutions for complex diseases.
Experience: 3+ years
Type: Hybrid

Parexel

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

Baxter

Skills & Focus: GST Operations, Safety Systems, Healthcare, Patient Care, Engineering, Medical Devices, Risk Management, Clinical Research, Supply Chain, Quality Assurance
About the Company: Baxter International is a global medical products company that specializes in supplying critical therapies for the treatment of complex medical conditions.
Type: Full time
Benefits: Our comprehensive benefits options reflect the value we place in our employees.

Chevron

Skills & Focus: Quality Assurance, Asset Integrity, Reliability Engineering, Robotics, Engineering, Consulting Services, Advanced NDE Inspections, Project Management, Continuous Improvement, Safety
About the Company: Chevron is a global leader in the energy sector, committed to delivering industry-leading results through innovation and operational excellence.
Experience: 7+ years of demonstrated supervisory experience within Oil & Gas or petrochemical industry
Type: Full-time
Benefits: Competitive compensation and benefits programs designed to meet employee needs.

Baxter

Skills & Focus: project management, hardware subsystems, product development, cross-functional teams, Agile methodologies, medical device industry, risk management, team leadership, communication skills, Six Sigma
About the Company: Baxter is a global medical products company that helps save and sustain lives through its innovative healthcare solutions.
Experience: 10+ years of experience, 5+ years in project management
Type: Full-time
Benefits: Support for Parents, Continuing Education, Professional Development, Employee Health & Well-Being, Paid Time Off, Volun…

Intuitive Surgical

Skills & Focus: clinical research, engineering leadership, medical devices, robotic systems, clinical studies, product development, regulatory compliance, patient safety, prototype evaluation, team management
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: 10+ years in medical device development, 5+ years in leadership
Type: Full-time

Baxter

Skills & Focus: Research and Development, Software Verification, Engineering, Healthcare Solutions, Product Development, Innovation, Medical Devices, Patient Care, Technology, Life Sciences
About the Company: Baxter is a global medical products and services company focused on saving and sustaining lives through innovative healthcare solutions.
Type: Full time
Benefits: Our comprehensive benefits options reflect the value we place in our employees.

Eclinical Solutions

Skills & Focus: Clinical Data Management, Database Design, Data Cleaning, Quality Control, Data Verification, Project Management, Client Relationship Management, ICH/GCP Guidelines, EDC Systems, Data Reporting Tools
About the Company: eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate…
Experience: 8-10 years of experience in Clinical Data Management

Alexion

Skills & Focus: statistical programming, SAS Programming, CDISC standards, datasets, tables, listings, figures, Good Clinical Practices, regulatory requirements, drug development
About the Company: At AstraZeneca, we champion diversity in a patient-driven, energizing, and kind culture where people build connections to explore new ideas that profoundly imp…
Experience: 2 to 4 years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry.

Alivecor

Skills & Focus: Quality, Regulatory, Complaints Management, Post-Market Surveillance, ISO 13485, Medical Devices, FDA, Customer Service, Troubleshooting, Risk Management
About the Company: AliveCor is a company pioneering over-the-counter medical ECG devices and advancing medical practice with artificial intelligence and machine learning, focusin…
Experience: 1-3 years in Medical Device industry or related field

Suki

Skills & Focus: AI voice solutions, clinical documentation, healthcare technology, medical documentation, post graduate training, patient care, AI algorithms, dynamic environment, digital health tools, strong analytical skills
About the Company: Suki is a leading technology company that provides AI voice solutions for healthcare, focused on reimagining the healthcare technology stack to lift the admini…
Experience: 4+ years of practice experience as a doctor, completion of at least one year of postgraduate training
Type: Hybrid (3 days in office, 2 days remote)
Benefits: Hybrid work model, opportunity to impact healthcare technology.

Intuitive Surgical

Skills & Focus: Project Management, Product Development, Cross-functional Collaboration, Risk Management, Design Control, Regulatory Submissions, Milestone Tracking, Quality Systems, Medical Devices, Process Improvement
About the Company: At Intuitive, we are committed to minimally invasive care through innovative robotic-assisted surgery technology. We foster an inclusive and diverse team dedic…

Precision Medicine Group

Skills & Focus: 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

Intuitive Surgical

Skills & Focus: Regulatory, Medical Devices, Global Regulatory Intelligence, EU MDR, clinical evaluation, Product claims, Regulatory submissions, EU Notified Body, Advertising and Promotion, Regulatory Trends
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: 10+ years
Type: Full-time

Precisionmedicinegroup

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

Precision Medicine Group

Skills & Focus: clinical monitoring, monitoring visit reports, protocols, SOPs, compliance, action items, safety, study performance, ICH GCP, training
About the Company: Precision Medicine Group is an Equal Opportunity Employer.
Experience: Minimum 3 years experience in clinical monitoring, clinical trial management or equivalent

Eclinical Solutions

QC Specialist Bengaluru
Skills & Focus: Quality Control, Biometrics, eCRFs, Data Management, Data Validation, ICH/GCP guidelines, clinical trial methodology, Medidata Rave EDC, SQL Server, Oracle
About the Company: eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate…
Experience: Minimum 3-5 years in Pharmaceutical/Biotechnology industry or equivalent

Intuitive Surgical

Skills & Focus: regulatory, medical devices, EU MDR, clinical evaluation, CE marking, global markets, regulatory submissions, compliance, regulatory intelligence, product portfolio
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: 10+ years
Type: Full-time

Iqvia

Skills & Focus: study design, edit specifications, quality delivery, eCRF, EDC build components, Study Authorization Form, Internal Design Review Meeting, database design, LLRR data, Rights and Roles
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.
Skills & Focus: medical review, adverse events, pharmacovigilance, safety data, clinical data, regulatory requirements, safety profiles, signal detection, aggregate reports, GCP
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Three (3) years experience practicing clinical medicine after award of medical degree.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.