All jobs at Applied Medical
Applied Medical logo

Regulatory Affairs and Quality Assurance (RA/QA) Associate Specialist

Applied Medical · South, KR
Posted Jul 9, 2026

<p style="margin: 0px; text-align: center;"><span style="font-size: 12pt; font-family: calibri, sans-serif;"><img src="https://appliedmedical.icims.com/icims2/servlet/icims2?module=AppInert&action=download&id=66&hashed=-1305937254" alt="Applied-Medical-Logo-w-Tag_H_Teal_cropped" /></span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: calibri, sans-serif;">As a new generation medical device company, we believe in the power of working together to make a meaningful and positive difference. Applied Medical is committed to improving the accessibility and affordability of high-quality healthcare globally.

We achieve this through a vertically integrated business model that enables our team members to develop technologies that enhance clinical care, while offering boundless opportunities for professional growth. We are dedicated to creating an environment where team members of diverse backgrounds are valued, challenged and acknowledged.

We are growing our Regulatory Affairs and Quality Assurance (RAQA) teams in Korea in order increase our regional partnerships so we can better serve the evolving needs of the Korean health system.</span></p> <br><strong>Position Description</strong><br><br><p style="margin: 0px;"><span style="font-family: Calibri, sans-serif; font-size: 12pt;">The Regulatory Affairs and Quality Assurance (RA/QA) Associate Specialist performs the day-to-day regulatory affairs and quality assurance responsibilities supporting Applied Medical's operations in Korea. This regulatory affairs specialist and quality assurance role keeps post-market surveillance, quality management system documentation, and product license activities compliant with local and international requirements.

The RA/QA Associate Specialist collaborates closely with the local RA/QA team, Applied Medical headquarters, and other business functions to maintain regulatory and quality compliance.</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 12pt;"><strong><span style="font-family: 'Calibri',sans-serif;">Key Responsibilities</span></strong></span></p><ul><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Handle post-market surveillance activities, including complaint handling, adverse event reporting, recalls, and related safety monitoring</span></li><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Maintain Quality Management System (QMS) documentation, including the RA/QA master, regulatory databases, material and batch classifications, labeling compliance, and external standards records</span></li><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Support product license approvals, including new product registrations, license amendments, renewals, and Korea Good Manufacturing Practice (KGMP) certifications</span></li><li><span style="font-size: 12pt;"><span style="font-family: 'Calibri',sans-serif;">Support Korea team to d</span><span style="font-family: 'Calibri',sans-serif;">evelop, implement, and maintain quality system compliance programs and procedures in accordance with Korean local requirements</span></span></li><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Collaborate with Applied Medical headquarters to maintain regulatory and quality compliance with international and local regulations</span></li><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Build constructive working relationships across business functions to achieve group and business goals</span></li></ul><p style="margin: 0px;"><span style="font-size: 12pt;"><strong><span style="font-family: 'Calibri',sans-serif;">Success in This Role Looks Like</span></strong></span></p><ul><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Maintaining accurate, audit-ready QMS and regulatory documentation</span></li><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Completing product registrations, amendments, and renewals on time and in compliance</span></li><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Resolving post-market surveillance activities promptly and accurately</span></li><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Applying sound judgment to analyze regulatory issues and generate effective solutions</span></li><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Building strong, cooperative relationships across the local team and headquarters</span></li><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Seeking and applying feedback to improve regulatory and quality processes</span></li></ul> <br><strong>Position Requirements</strong><br><br><p style="margin: 0px;"><span style="font-size: 12pt;"><strong><span style="font-family: 'Calibri',sans-serif;">This position requires the following skills and attributes:</span></strong></span></p><ul><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Bachelor's degree or higher in medical device engineering, biotechnology, pharmacy, science, or a related field</span></li><li><span style="font-size: 12pt;"><span style="font-family: 'Calibri',sans-serif;">One to three years of experience in regulatory affairs and quality assurance within the medical device industry</span><span style="font-family: 'Calibri',sans-serif;"> (Fresh graduates with relevant internship experience may be considered)</span></span></li><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Strong understanding of Korean medical device regulations and Ministry of Food and Drug Safety (MFDS) requirements</span></li><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Fluent written and spoken English for effective communication with Applied Medical headquarters</span></li><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Strong analytical and problem-solving skills</span></li><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Ability to work collaboratively across teams and business functions</span></li></ul> <br><strong>Preferred</strong><br><br><p style="margin: 0px;"><span style="font-size: 12pt;"><strong><span style="font-family: 'Calibri',sans-serif;">The following skills and attributes are preferred:</span></strong></span></p><ul><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Experience with KGMP audits and product license submissions</span></li><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">NIDS RAC holder</span></li><li><span style="font-family: Calibri, sans-serif; font-size: 12pt;">Continuous learning mindset with a focus on professional development</span></li></ul> <br><br><strong>Benefits</strong><br><br><p style="margin: 0px;"><span style="font-size: 12pt; font-family: calibri, sans-serif;">Applied offers benefits package following Korean labor laws</span></p>

Originally posted by Applied Medical. View original posting

← Browse all companies

BioCareerAI is an independent job platform and is not affiliated with or endorsed by Applied Medical.

Regulatory Affairs and Quality Assurance (RA/QA) Associate Specialist at Applied Medical | BioCareerAI