Last updated: 2025-05-22

18 Quality Engineering jobs in Seoul.

Hiring now: Functional Leader In Manu @ Biogen, Sr Quality Management Spe @ Lunit, Head Of Clinical Research @ Intuitive , Pv Operational Associate @ Abbvie, Medtech Associate Commerc @ Johnson Jo, Sr Cra I Fsp Korea @ Syneos Hea, Quality Compliance Mgr @ Amgen, Sr Regulatory Affairs Spe @ Novo Nordi.Explore more at at kaamvaam.com

🔥 Skills

Medical Device (3) Process Improvement (3) GMP (3) medical devices (2) ISO 13485 (2) MDSAP (2) EU MDR (2) UKCA (2) Quality Management System (2) Regulatory Compliance (2)

📍 Locations

Seoul (16) Incheon (2)

Biogen

Skills & Focus: pharmaceutical manufacturing, biologics manufacturing, Continuous Process Verification, supplier relationship management, CDMO, CLO, technical expertise, process control strategy, business performance reviews, cGXP regulations
About the Company: Biogen is a biotechnology company that discovers, develops, and delivers innovative therapies for people living with serious neurological and neurodegenerative…
Experience: Deep experience in integrating related disciplinary knowledge with a strong technical background in pharmaceutical/biologics manufacturing.
Type: Full-time

Lunit

Skills & Focus: quality management system, medical devices, software medical devices, ISO 13485, MDSAP, EU MDR, UKCA, internal audit, external audit, CAPA process
About the Company: Lunit, short for 'Learning Unit', is a medical AI company that develops and offers AI solutions contributing to cancer diagnosis and treatment.
Experience: 10 years or more in quality management system operation and management within medical device or in vitro diagnostic industries.
Salary: Negotiable after interview
Type: Full-time
Benefits: Various benefits including meal support, equipment allowances, participation in conferences and training, and health ch…
Skills & Focus: Quality Management System, Medical Device, In-vitro Diagnostics, KGMP, ISO 13485, MDSAP, EU MDR/IVDR, UKCA, Regulatory Compliance, AI in Healthcare
About the Company: Lunit is a medical AI company that develops and provides AI solutions for cancer diagnosis and treatment.
Experience: At least 1 year of experience in quality management system operation and management at a medical device or in-vitro diagnostic medical device manufacturer.
Salary: Negotiable after interview
Type: Contract
Benefits: Benefits include meal allowances, unlimited snacks, desk decoration support, attendance support for conferences, traini…

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
Skills & Focus: SCM, warehouse management, 3PL, inventory reconciliation, KMDIA, data validation, medical device, regulations, cycle counting, customs audit
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: Minimum Bachelor’s degree or equivalent Work experience in warehouse management, demand planning or SCM in Medical device industry is preferred

Abbvie

Skills & Focus: pharmacovigilance, PV system performance, regulatory inspections, adverse events, safety reports, Compliance, metrics, Quality Management System, literature review, audits
About the Company: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tom…
Experience: A minimum of 3 years of experience within pharmacovigilance or a related field
Type: Full-time

Lunit

Skills & Focus: Regulatory Affairs, Medical Device, Cancer Diagnosis, Business Growth, FDA Compliance, European Market Regulations, Communication Skills, AI Technology, Medical Regulations, Clinical Regulatory Experience
About the Company: Lunit is a healthcare AI company that develops and provides AI solutions that contribute to cancer diagnosis and treatment.
Experience: 15 years or more in the field of medical device Regulatory Affairs
Salary: Negotiable after the interview
Type: Full-time
Benefits: Lunch and dinner meal allowance, unlimited snacks, support for desk decoration costs, high-spec computer equipment, tra…
Skills & Focus: Medical Device Development, Project Management, Cross-Functional Collaboration, Risk Management, Quality Assurance, Regulatory Compliance, Stakeholder Communication, Resource Allocation, Strategic Oversight, Process Improvement
About the Company: Lunit, derived from the term 'Learning Unit', is a medical AI company that develops and provides AI solutions for cancer diagnosis and treatment. The goal is t…
Experience: Minimum of 5 years in the medical device industry, with at least 2 years of experience managing medical device development projects
Salary: After Negotiation
Type: Full Time
Benefits: Meal Allowance, Workspace Decoration Budget, Latest Computer Equipment, Seminar and Book Support, Health Check-ups, Pai…

Johnson & Johnson

Skills & Focus: quality compliance, supply chain, quality management, regulatory compliance, Good Distribution Practices, GMP, ISO 9001, analysis, collaboration, customer focused
About the Company: Johnson & Johnson is a leading global healthcare company dedicated to innovation in healthcare solutions across various segments.
Experience: At least 7+ years of experience in regulated industry, preferably in Quality Control, Quality Assurance, or Supply Chain.
Type: Regular

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…
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

Syneos Health

Skills & Focus: clinical research, site qualification, site management, ICH-GCP, clinical data integrity, source document review, investigational product, GCP regulations, patient recruitment, clinical monitoring
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.

Amgen

Skills & Focus: quality oversight, clinical trials, risk management, compliance, data integrity, Quality Management Systems, inspection readiness, protocol development, regulatory submissions, stakeholder communication
About the Company: Amgen is a leading biotechnology company, focused on improving lives through innovative medicines.
Experience: Minimum 5 years in pharmaceutical industry with 3 years or more in Quality Management.
Type: Full time

Syneos Health

Skills & Focus: Clinical Operations, Trial Master File, GCP, ICH Guidelines, ALCOA, Document Management, Administrative Support, Quality Assurance, Data Analysis, Team Collaboration
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Type: Intern

Novo Nordisk

Skills & Focus: regulatory affairs, compliance, pharmacovigilance, NDA, GMP, stakeholders, team collaboration, product registration, regulatory submissions, analytical skills
About the Company: Novo Nordisk is a global healthcare company specializing in diabetes care and other serious chronic conditions.
Experience: 5+ years
Type: Full-time

Johnson & Johnson

Skills & Focus: Regulatory Affairs, Medical Device, Regulatory Environment, Compliance, Applications, Certification, Process Improvement, Stakeholder Communication, Requirements, Submission
About the Company: Johnson & Johnson is a multinational corporation that develops medical devices, pharmaceuticals, and consumer packaged goods.
Experience: Minimum 2 years of progressive RA experience in Medical Device Industry
Type: Fixed Term (1 year)
Skills & Focus: manufacturing sciences, technology transfer, process validation, product strategy, life cycle management, technical support, quality deviations, health authorities, external site, drug substance
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: Proven track record in large molecules in at least three of these areas: process development, new product introduction, technology transfer, process validation and/or ongoing production support.
Type: Fully Onsite
Skills & Focus: Quality Control, Laboratory Activity, GMP, Data Integrity, Laboratory Management, Electronic Systems, Equipment Management, Housekeeping, Team Collaboration, Safety Requirements
About the Company: Johnson & Johnson is a leading healthcare company dedicated to improving health through innovative science and technology across the full spectrum of healthcar…
Type: Fixed Term (1 year)