Join our dynamic team where innovation and care converge in a culture that values continuous learning, diversity and transformative career development. Underpinned by THRIVE with Zuellig Pharma, our commitment to transforming the way we grow, care and succeed together as one organization, we are dedicated to helping our people make a meaningful impact in healthcare.
RA Specialist
Korea, Republic of
Zuellig Pharma is a leading healthcare solutions company in Asia, and our purpose is to make healthcare more accessible to the communities we serve. We provide world-class distribution, digital, and commercial services to support the growing healthcare needs in this region.
The company was started a hundred years ago and has grown to become a multibillion-dollar business covering 17 markets with over 12,000 employees. Our people serve more than 200,000 medical facilities and work with over 450 clients, including the top 20 pharmaceutical companies in the world.
Purpose of The Role:
The Regulatory Affairs (RA) Specialist is responsible for effectively executing regulatory strategies and activities to meet business objectives and legal requirements in Korea.
What You’ll Do:
- Maintain product licenses by managing RA activities, and ensure compliance with local laws, regulations, and guidelines by monitoring and adhering to internal Standard Operating Procedures (SOPs).
- Serve as a liaison between regulatory bodies and the company’s operating divisions.
- Prepare and submit applications and reports to applicable regulatory agencies.
- Respond to requests for information from regulatory bodies.
- Participate in regional RA projects and respond to queries in a timely manner based on local regulations.
- Monitor regulatory trends and assess the impact of any changes on company operations.
- Develop and maintain professional relationships with federal, state, and local regulatory agencies.
- Independently manage all RA activities to support commercial success and ensure strict compliance with local regulations.
- Communicate regulatory plans and strategies to all stakeholders, and propose optimal solutions from a regulatory perspective to minimize any commercial impact during urgent situations.
- Support the reporting of adverse events.
Must-Have:
- Education : Bachelor’s degree major in Biochemistry, Pharmacy, Biological Sciences, Life Sciences, or a related field.
- Language : Business-level English proficiency.
- Experience :
- 3-6 years experience in Regulatory Affairs(RA) for pharmaceutical products.
- At least 3 years of experience working within a Multinational Corporation(MNC).
What Will Make You Successful:
- Excellent command of both spoken and written English.
- Strong communication and negotiation skills with internal teams, external partners, and Health Authorities (MFDS).
- Passion for new business development and a proactive willingness to overcome challenges.
- Extensive and up-to-date knowledge of applicable government regulations.
- Ability to effectively inform and educate managers and department heads on compliance regulations and policies.
- Outstanding analytical, problem-solving, and strategic planning skills.
- Proficiency with MS Office Suite and Hangul (HWP).
- Strong team player with a collaborative mindset.
What We Offer:
- We are committed to fostering an inclusive environment where our employees can learn, grow, and achieve shared success.
- We champion diversity, equity, and inclusion, ensuring every individual feels valued, respected, and treated fairly.
- As a leading multi-market healthcare solutions provider, we empower our employees to gain comprehensive knowledge and expertise in the dynamic healthcare industry across the region.
- Enjoy the flexibility to effectively balance your work and personal life while taking charge of your career journey through our empowering growth opportunities.
- Our Total Rewards program is designed to support your overall well-being in every aspect.
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