Novo Nordisk is hiring a senior regulatory affairs specialist in Seoul, South Korea. Reporting directly to the Regulatory Affairs Manager, this role was recently created as part of the team expansion.
Job Information
Depending on the candidate’s experience level, the job title for this post will either be RA Specialist or Sr. RA Specialist. This job is permanent. The chosen applicant will guarantee that products are maintained and satisfy both internal and external compliance standards, as well as that they can be put on the market with the best possible but legal claims, advertising, and promotion in accordance with business strategies. As a productive member of a designated local regulatory team, you will also interact with the external regulatory environment within a designated area of accountability, be a proactive partner to other stakeholders, and represent Novo Nordisk Korea before local regulators, trade associations, and other important external regulatory bodies.
Qualifications
- A pharmacist license is required, as is at least five years of experience working on regulatory submissions and clearances.
- It is essential to have work experience with GMP inspection and new product registration.
- Experience with regulations in a global corporation is advantageous.
- possesses excellent analytical thinking, time management, and problem-solving abilities.
- demonstrates effective communication skills and a strong knowledge of the English language.
Application
For more details and application, visit Novo Nordisk’s official website.
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