[Skip to main content](#main-content) [OpenNash Jobs](https://jobs.opennash.com/) [Hiring report](/reports/hiring/) · [All Medtronic jobs](https://jobs.opennash.com/companies/medtronic/) · [Search jobs](/search/) Medtronic · Multiple locations # Regulatory Affairs Operations Specialist – Korean Bilingual Multiple locations Legal & Compliance Listed on Medtronic’s official careers site. Posted October 15, 2026. Check that it is still open and apply there. [Apply on Medtronic’s careers site →](https://medtronic.wd1.myworkdayjobs.com/MedtronicCareers/job/Ho-Chi-Minh-City-Ho-Chi-Minh-City-Vietnam/Regulatory-Affairs-Operations-Specialist---Korean-Bilingual_R74807-1) [OpenNash Jobs](https://jobs.opennash.com/) / [Medtronic](https://jobs.opennash.com/companies/medtronic/) / Regulatory Affairs Operations Specialist – Korean Bilingual ## Job description Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life The Regulatory Operations function supports the preparation, coordination, submission, tracking, and maintenance of regulatory documentation required to support product registrations and compliance activities across global markets. This team partners with cross-functional stakeholders to help ensure regulatory submissions are accurate, complete, and aligned with applicable requirements, while driving process efficiency and maintaining regulatory records and systems. The Regulatory Operations Specialist (Korean Bilingual) supports regulatory submission and compliance activities by coordinating documentation, managing regulatory records, and collaborating with stakeholders across multiple functions. This role requires Korean language proficiency, knowledge of regulatory requirements in Korea, and the ability to manage multiple submissions and regulatory processes while maintaining accuracy and compliance. ### Primary Responsibilities Coordinate the preparation, compilation, review, and submission of regulatory documentation required for registrations, renewals, amendments, annual reports, and other regulatory activities. Manage the tracking, indexing, archiving, and maintenance of paper and electronic regulatory records and submissions. Review submission documentation for completeness, accuracy, and compliance with applicable regulatory requirements and internal standards. Collaborate with cross-functional stakeholders to collect, organize, and maintain documentation supporting regulatory filings. Monitor regulatory activities, submission timelines, and system records to support compliance and reporting requirements. Support regulatory labeling activities by providing recommendations aligned with applicable regulatory requirements. Maintain regulatory databases, systems, and tools to ensure accurate documentation and traceability of regulatory information. Monitor regulatory changes and communicate relevant updates that may impact submission strategies, processes, or compliance activities. ### Required Qualifications Bachelor's Degree in Medical Sciences, Biological Sciences, Engineering, or a related technical discipline and a minimum of 3 years of regulatory, regulatory operations, quality, clinical, or related experience within a medical device, pharmaceutical, contract research organization (CRO), or similar regulated environment. Business-level English proficiency in reading, writing, and speaking. Korean language proficiency equivalent to TOPIK II Level 3 or Level 4, with the ability to read, write, and communicate professionally in Korean. Knowledge of Korean regulatory requirements and regulatory submission processes. Proficiency with Microsoft Office applications, including Excel, Word, and PowerPoint. ### Preferred Qualifications Experience supporting regulatory submissions, registrations, renewals, or compliance activities for medical devices. Experience working with global stakeholders across multiple regions and functions. Experience using regulatory information management systems, document management systems, SAP, SharePoint, or similar business applications. Knowledge of medical device regulatory frameworks within Asia-Pacific (APAC), the United States (US), or the European Union (EU). Experience applying process improvement methodologies such as Define, Measure, Analyze, Improve, and Control (DMAIC) or similar continuous improvement approaches. Physical ### Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. ‌ Recruitment Fraud Alert We are aware of phishing scams targeting job seekers. ### Please keep the following in mind Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses. Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate. If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments. If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com. ‌ Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). ## At a glance - Posted by the employer: Oct 15, 2026 - First seen by OpenNash: Oct 12, 2026 - Last checked: Oct 19, 2026 - Listed for: 7 days - Location: Multiple locations[Apply on Medtronic’s careers site →](https://medtronic.wd1.myworkdayjobs.com/MedtronicCareers/job/Ho-Chi-Minh-City-Ho-Chi-Minh-City-Vietnam/Regulatory-Affairs-Operations-Specialist---Korean-Bilingual_R74807-1) ## More jobs at Medtronic ### [Associate Regulatory Affairs Specialist](https://jobs.opennash.com/companies/medtronic/jobs/757d0aae65c665132f32/) ### [Principal Legal Counsel, Global Trade Legal & Compliance (Import)](https://jobs.opennash.com/companies/medtronic/jobs/bb6794fa15620529c85e/) ### [Principal Regulatory Affairs Specialist](https://jobs.opennash.com/companies/medtronic/jobs/e71124965e8ea001974b/) ### [Senior Principal Legal Counsel, Global Trade Legal & Compliance (Export)](https://jobs.opennash.com/companies/medtronic/jobs/8a9fac84556342985165/) ### [Sr. Compliance Manager, Global Trade Legal & Compliance](https://jobs.opennash.com/companies/medtronic/jobs/3806c40cf04421eac7d7/) ## Similar jobs at other companies ### [Associate Manager, Regulatory Affairs](https://jobs.opennash.com/companies/international-flavors-fragrances/jobs/36e82959c5862210b88a/) International Flavors & Fragrances ### [Director, Regulatory Affairs – Abbott Nutrition China](https://jobs.opennash.com/companies/abbott-laboratories/jobs/4e8c957607c2af6eb5a6/) Abbott Laboratories ### [Senior Manager Regulatory Affairs Advertising and Promotion](https://jobs.opennash.com/companies/sanofi/jobs/4dea6340d9f2393cd59e/) Sanofi ### [Regulatory Affairs Compliance Manager](https://jobs.opennash.com/companies/pbf-energy/jobs/91b1d27d5c2bfeb75910/) PBF Energy OpenNash lists jobs from employers’ own careers sites and does not handle applications. Dates come from the employer where stated; “first seen” and “last checked” are our own observations. OpenNash Jobs · Official listings with dates and links to the employer. [Weekly hiring report](/reports/hiring/) · [Methodology](/methodology/)