39 QA Engineering Jobs in Seoul, South Korea

Role highlights

• Demonstrated experience in internal and external audits, regulatory inspections, Product Quality Complaint (PQC) handling, Nonconformance a…
• Required Skills: Preferred Skills: Audit Management, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Data Analy…

Role highlights

• Assist with cross-functional QA projects and support QMS-related systems and documentation.
• Perform other QA administrative and operational tasks as assigned.

Role highlights

• Manage quality incidents, implement corrective and preventive actions, and maintain continuous review and examination readiness.
• Collaborator Mentorship: Provide patient safety mentorship to local functions (Marketing, Sales, Regulatory Affairs, Medical Affairs) on is…

Role highlights

• Support RA manager in developing regulatory strategies.
• CORE JOB RESPONSIBILITIES Developing RA strategies - assess timeline and lead development of regulatory strategy for new assets and line…

Role highlights

• Conducts site evaluation, site training, routine, and site closure monitoring activities with compliance to the protocol and monitoring pla…
• Advanced knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies.

Role highlights

• Qualifications 4+ years of experience in Regulatory Affairs, Quality Assurance, or a related medical devices industry function preferred.
• Specialist, Quality & Regulatory Affairs supports the implementation and maintenance of regulatory and quality compliance programs to ensur…

Role highlights

• CRA I Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard…
• Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client…

Role highlights

• Knowledge, Skills and Abilities: Effective clinical monitoring skills Demonstrated understanding of medical/therapeutic area knowledge and…
• Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities .Assess investigationa…

Role highlights

• Quality Engineering skills including a thorough understanding of industry regulations and basic statistical methods for Quality Assurance (…
• Ensure existence of the applicable audit/visit CDA (Confidentiality Disclosure Agreement) Accompany customers to site audits, when appropri…

Role highlights

• 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…

Role highlights

• Advanced level of competency or experience in providing contextual information on the clinical trials, connecting stakeholders to the inves…
• Conducts site evaluation, site training, routine on-site and off-site monitoring, and site closure monitoring activities with compliance to…

Role highlights

• Actively participate in Investigator and other external or internal meetings and audits & regulatory inspections as required.
• Actively participate in Investigator and other external or internal meetings, audits & regulatory inspections Work in a self-driven capacit…

Role highlights

• Demonstrated experience in internal and external audits, regulatory inspections, Product Quality Complaint (PQC) handling, Nonconformance a…
• Essential Job Duties and Responsibilities [Quality Systems] Ensure appropriate change control procedures are followed.

Role highlights

• Manage quality incidents, implement corrective and preventive actions, and maintain continuous review and examination readiness.
• Collaborator Mentorship: Provide patient safety mentorship to local functions (Marketing, Sales, Regulatory Affairs, Medical Affairs) on is…

Role highlights

• Resolve Product Quality and Compliance Issues and contribute to continuous improvement through Deviation, Complaints, Change management, CA…
• The key role of this job is to execute sustainable Quality Management System to be aligned with Viatris Global policy…

Role highlights

• QC and Laboratory Support Lead annual quality projects related to local QC testing and contract laboratories, including method transfer, te…
• Manage quality requirements for product launches, lifecycle changes, and continuous improvement initiatives that strengthen the local quali…

Role highlights

• Laboratoire Guerbet Regulatory Affairs Manager M/F ( 30861 ) At Guerbet, we build lasting relationships so that to enable people…
• Experience leading cross-functional projects and regulatory authority interactions.

Role highlights

• Serve as an advisory expert on Product Compliance during new product introductions, investment projects, and other initiatives, ensuring th…
• While maintaining the capacity and flexibility to accommodate new regulatory initiatives driven by product portfolio developments and proje…

Role highlights

• Ensure GMP and SHE requirements are adhered at all the time To ensure workstation are clean and orderly Support the…
• GMP and SHE (Safety Health and Environmental) compliance .

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• Translate customer challenges in quality, document control, supplier governance, audits, compliance, and operations into clear solution des…
• Nice to Have Direct experience with QMS, document control, audit management, supplier quality, PLM, or manufacturing compliance solutions.

Role highlights

• 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.

Role highlights

• What you will do : Perform production release activities as a Quality Assurance representative in accordance with company policies, procedu…
• The Quality Specialist is responsible for QMS support to the Senior Quality Manager to ensure compliant execution, monitoring, and continuo…

Role highlights

• 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…

Role highlights

• 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…