# [MedTech] Sr. Regulatory Affairs Specialist (Contractor) at Johnson & Johnson

Johnson & Johnson is hiring a [MedTech] Sr. Regulatory Affairs Specialist (Contractor) in Seoul, South Korea. Level rates it Little AI ●○○○; you can [apply on Johnson & Johnson](https://jobsbylevel.com/go/d5ba7db4-6264-437e-8d65-7a03c286b386?utm_medium=ai-agent).

AI Level 1, AI centrality 37 out of 100. Seoul, Korea, Republic of.

## Details

- Company: [Johnson & Johnson](https://jobsbylevel.com/companies/johnson-johnson)
- AI level: AI Level 1 (score 37 out of 100)
- Location: Seoul, Korea, Republic of
- Posted: November 4, 2026
- Apply: https://jobsbylevel.com/go/d5ba7db4-6264-437e-8d65-7a03c286b386?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=medtech-sr-regulatory-affairs-specialist-contractor-at-johnson-johnson-63ac9a

## Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Regulatory Affairs Group Job Sub Function: Regulatory Affairs Job Category: Professional All Job Posting Locations: Seoul, Korea, Republic of Job Description: About MedTech Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech We are searching for the best talent for Sr. RA Specialist to be in Seoul. Position Summary: Coordinates, compiles, and submits applications of new products or changes to the approved products to the regulatory agencies. Ensures compliance with regulatory agency regulations and interpretations. Prepares responses to regulatory agencies' questions and other correspondence. Gathers and assembles information necessary for submissions in accordance with regulations and relevant guidelines. Involved with the preparation of necessary outlines, summaries, status reports, memos, graphs, charts, tables, and slides. Provides solutions to a variety of problems of moderate scope and complexity. Organizes and maintains reporting schedules of new product registration, changes in products, projects, etc. You will be responsible for: Functional and Technical Competencies Prepares, submits, and monitors applications of new products, changes, renewals in approved products, and KGMP. Applies knowledge in regulations and characteristics of products to prepare compliant regulatory strategies and to assess regulatory impact on products as product life-cycle management. Interacts with regulatory agency personnel in order to expedite approval applications and to resolve regulatory matters with limited supervision. Follows up of mandatory requirements for registration: local certificates, importation of samples, local testing, etc. with limited supervision. Ensures Korean label contents and approves the final Korean label artwork. Researches and consolidates regulatory requirements and actively communicates with the supervisor and the manager. Provides training and limited supervision of contract resources, as needed. Supports and contributes to team, company, regional, global, cross-sector projects. Shares best practices and learnings with the team in terms of RA processes and templates, product registration, projects, etc. Conforms regulatory compliance including but not limited to promotional material review and regulatory impact assessment. Leverages experience and learnings from the past to make reasonable decisions in the challenging situations. Understands business environment and business strategies and develops effective and results-oriented regulatory strategic plans that are in line with business objectives. Manages specific project steps to meet milestones independently or with limited supervision. Understands trends in the healthcare environment, changes in external marketplace, and competitors’ tendency and the influence of social, economic, and political factors on business and regulatory environment. Leadership Competencies Effectively manages priorities and strongly

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/medtech-sr-regulatory-affairs-specialist-contractor-at-johnson-johnson-63ac9a

Source: https://jobsbylevel.com/jobs/medtech-sr-regulatory-affairs-specialist-contractor-at-johnson-johnson-63ac9a

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Level. https://jobsbylevel.com/jobs/medtech-sr-regulatory-affairs-specialist-contractor-at-johnson-johnson-63ac9a.

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