Project Controller

Posted 2 Days Ago
Be an Early Applicant
2 Locations
In-Office or Remote
Entry level
Other
The Role
Manage end-to-end medical device certification projects for Korean manufacturers, coordinating applications, certification planning, audits, technical documentation assessments, schedules, invoicing, and certificate issuance. Serve as the connection between customers, auditors, technical reviewers, and DNV’s global certification team while ensuring regulatory compliance, accurate project data, deadlines, and strong customer experience.
Summary Generated by Built In

Are you ready to take ownership of certification projects that bring safe, innovative medical devices to patients worldwide? DNV Medical Devices is looking for a Project Controller to join our Project & Customer Management Team in Seoul.

In this role, you will manage medical device certification projects under EU MDR, EU IVDR, MDSAP and ISO 13485, from the first client application through to certificate issuance. You will be the key link between Korean manufacturers, our auditors and technical reviewers, and DNV's Global Certification Unit (GCU), making sure every project is delivered on time, in compliance with regulatory and accreditation requirements, and with an excellent customer experience.

This is a one year time-bound contract opportunity, and interested candidates are encouraged to apply at the earliest.

  • Manage certification projects end to end, from application review, certification planning and agreements through to certificate issuance.
  • Plan and coordinate schedules of QMS audits, technical documentation assessments with auditors/assessors and customers.
  • Keep project data accurate in DNV's production systems, and manage invoicing.

You will join the team in Korea supporting a portfolio - hundreds of Korean medical device manufacturers seeking access to the EU and global markets. You will work with the local connections in Korea and global connections in Europe.

  • The opportunity to work at one of the world's leading notified bodies, at the heart of medical device regulation.
  • Hands-on exposure to EU MDR, EU IVDR, MDSAP and ISO 13485 certification across a wide range of devices and manufacturers.
  • An international working environment with daily collaboration across DNV's global Medical Devices network.
  • Structured onboarding and continuous learning to build your regulatory and certification expertise.

Responsibilities
  • We offer flexible work arrangements that help employees maintain a healthy balance between professional and personal life while staying productive.
  • Paid leave includes annual and special leave for rest and personal needs.
  • Medical benefits cover routine check-ups for continued wellness.
  • Financial security is ensured through life, health (accident/illness), and travel insurance.
  • Professional growth is supported through training sponsorships, structured programs, and on-the-job learning.

*Benefits may vary depending on role, employment type, tenure, or grade level. *

DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity.

Qualifications

  • Bachelor's degree, or equivalent professional experience.
  • Fluency in Korean and strong written and spoken English
  • Ability to manage multiple projects at once and meet firm deadlines

  • Experience at a notified body, certification body or regulatory consultancy
    Auditing experience or knowledge of MDR, MDSAP, and ISO certification schemes

  • Structured, detail-oriented and reliable
  • Customer-focused, with clear and confident communication
  • A team player who is comfortable working in a global organization
 
Security and compliance with statutory requirements in the countries in which we operate is essential for DNV. Background checks will be conducted on all final candidates as part of the offer process, in accordance with applicable country-specific laws and practices.
About Us

About Life Sciences

 

We help our customers in medical devices, healthcare, and aquaculture/ocean industries build trust and transparency across their products, assets, and supply chains. By working with customers to certify medical technologies, support safe and sustainable healthcare practices, and advance responsible aquaculture and ocean stewardship, we help manage risks, meet regulatory demands, and achieve long-term goals. Drawing on deep technical expertise, we partner with customers worldwide to bridge trust gaps between patients, providers, producers, and consumers—driving sustainable results and improved ESG performance.

Skills Required

  • Bachelor’s degree or equivalent professional experience
  • Fluency in Korean
  • Strong written and spoken English
  • Ability to manage multiple projects simultaneously and meet firm deadlines
  • Experience at a notified body, certification body, or regulatory consultancy
  • Auditing experience or knowledge of MDR, MDSAP, and ISO certification schemes
  • Structured, detail-oriented, and reliable working style
  • Customer-focused communication skills
  • Clear and confident communication
  • Ability to work collaboratively in a global organization
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The Company
HQ: Bærum
15,000 Employees

What We Do

DNV is the independent expert in risk management and assurance, operating in more than 100 countries. Through its broad experience and deep expertise DNV advances safety and sustainable performance, sets industry benchmarks, and inspires and invents solutions.

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