Last updated 2026-07-05
23 QA Engineering Jobs in Seoul, 11, South Korea
Browse 23 QA Engineering jobs across Seoul, 11, South Korea. Listings are updated hourly and include salary data where available.
Market data for QA Engineering jobs in Seoul, 11, South Korea
Professionals focused on ensuring product quality, compliance, and process improvement across various engineering and manufacturing sectors.
Companies with current QA Engineering listings
| Company | Active jobs |
|---|---|
| AstraZeneca | 3 |
| 3610 Becton Dickinson Korea Limited | 2 |
| Abbott Laboratories | 2 |
| Becton Dickinson & Company | 2 |
| Fortrea | 2 |
| Novonordisk | 2 |
| 622 GlaxoSmithKline Korea Limited | 1 |
QA Engineering jobs by schedule
QA Engineering jobs by seniority
Common QA Engineering job titles
FAQ
- How many QA Engineering jobs are listed in Seoul, 11, South Korea?
- This page currently shows 23 QA Engineering jobs in Seoul, 11, South Korea.
- Which companies are hiring for QA Engineering roles in Seoul, 11, South Korea?
- Current listings include roles from AstraZeneca (3 jobs, 13%), 3610 Becton Dickinson Korea Limited (2 jobs, 9%), Abbott Laboratories (2 jobs, 9%), Becton Dickinson & Company (2 jobs, 9%), and Fortrea (2 jobs, 9%).
- What seniority levels are common for QA Engineering jobs in Seoul, 11, South Korea?
- The visible seniority mix includes Mid (13 jobs, 57%), Senior (6 jobs, 26%), and Entry (4 jobs, 17%).
- What work schedules are common for QA Engineering jobs in Seoul, 11, South Korea?
- The visible schedule mix includes Full time (21 jobs, 91%) and Contract (2 jobs, 9%).
- What QA Engineering job titles are common in Seoul, 11, South Korea?
- Common titles include Clinical Research Associate (2 jobs, 9%), RA Specialist (2 jobs, 9%), RAPA Manager (2 jobs, 9%), Sr. Quality Specialist (1.6yr, Contractor) (2 jobs, 9%), and Analytical Operations Specialist (1Y 8M, Replacement of maternity leave) (1 job, 4%).
- What does this market snapshot include?
- Most visible listings are full-time (21 of 23). Mid-level roles account for 13 of 23 listings.
Snapshot updated 52m ago
Quality Manager
- Lead the Quality Management Review (QMR) process, ensuring systematic review of quality performance, risks, compliance status, and continua…
- Experience in GMP, GDP, GLP, GSP and QMS.
Analytical Operations Specialist (1Y 8M, Replacement of maternity leave)
- Third Party Laboratory Management including incident management KPI/Performance review Contract management Support global team for Quality…
- Analytical Method Transfer management Overall planning and management of new products and life-cycle-management AMTs Korea SPOC 9.
Danaher
Jun 23- The Quality Specialist is responsible for QMS support to the Senior Quality Manager to ensure compliant execution, monitoring, and continuo…
- What you will do : Perform production release activities as a Quality Assurance representative in accordance with company policies, procedu…
Thermo Fisher Scientific
Jun 22- Knowledge, Skills and Abilities: Effective clinical monitoring skills Excellent understanding and demonstrated application of FDA guideline…
- Manages Risk Based Monitoring concepts and processes Ability to mentor and train other monitors in a positive and effective manner…
[MedTech] RA Assistant – Special Projects
- Required Skills: Preferred Skills: Analytical Reasoning, Business Writing, Communication, Data Analysis, Detail-Oriented, Document Manageme…
- You will be responsible for: Supports the RA team in projects, including updating and maintaining data in RA system.
Wacker
Jun 17- Managing documentation related to quality, IMS, process and chemical safety, and MOC matters, including audit preparation.
- Providing production support in Ulsan, addressing product and raw material quality concerns, as well as process optimization.
Regulatory Affairs Specialist
- The Impact You’ll Make in this Role As a Regulatory Affairs Specialist, you will have the opportunity to tap into…
- Coordinate with internal cross‑functional stakeholders (Global Regulatory Affairs, Quality, Supply Chain, and Commercial teams) to support…
Fortrea
Jun 12- Regulatory Submissions Associate Manager II - APAC Job Overview: In the role you will collaborate with key stakeholders across the…
- Experience in RA, IRB/EC, and Third Body submissions, including submission strategy, timeline, and planning Solid expertise in QC of regula…
More roles at Fortrea
Zimmer Biomet Korea Ltd
Jun 11- Requirements * Expected Areas of Competence Competent English language skills (reading, writing, listening, and fluent speaking) Comprehens…
- New product registration & Maintenance of existing product licenses Compliance with MFDS & Corporate QA requirements Principal Duties & Res…
Roche
Jun 10- Cross-Functional Collaboration: Act as the proactive RA expert on project teams, driving alignment and collaborating effectively with globa…
- Develop and execute regulatory Core Competencies: Proactive, self-motivated professional with strong strategic thinking and problem-solving…
Novonordisk
Jun 9- Analyze regulatory issues and communicate effectively with key stakeholders, including global colleagues.
- Other role tasks are as follows but not limited to: Lead the preparation of regulatory documents, dossiers, and applications to…
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AstraZeneca
Jun 9- Study Start-Up and Regulatory Maintenance: In applicable countries, lead or support site qualification, document collection and submissions…
- Continuous Improvement: Champion more efficient and effective methods to deliver quality clinical trials with reduced budget and timelines,…
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Sr. Quality Specialist (1.6yr, Contractor)
- Job Description I. Position Summary This position is responsible for managing and ensuring that distribution quality and the quality system…
- G. Lead and /or facilitate and support Country, Regional and Corporate Quality Projects.
More roles at 3610 Becton Dickinson Korea Limited
Sr. Quality Specialist (1.6yr, Contractor)
- Quality Specialist (1.6yr, Contractor) Company: Becton Dickinson & Company We are the people who give possibilities purpose BD is one…
- Job Description I. Position Summary This position is responsible for managing and ensuring that distribution quality and the quality system…
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Abbott Laboratories
May 15- Good English writing and speaking skills Excellent computer usage skills BACKGROUND: Knowledge and experience of the regulatory affairs a…
- 대치동 PRIMARY FUNCTION/PRIMARY GOALS/OBJECTIVES: Prepare documentation for product registration/license/approval in accordance with registrat…
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Amgen
Apr 17- This position plays a key role in the clinical trial application management, import licenses and regulatory agency inspections at Amgen.
- Attends to project meetings with cross functional department leads to provide strategy, timelines and requirements for regulatory submissio…