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.
Regulatory Affairs Manager
Viet Nam
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.
Working Location: Ha Noi
Purpose of The Role:
- To manage all regulatory issues in relation products’ registration and company registration in line with MOH regulation
- To provide technical support across the region as required in relation to product registration
What You’ll Do:
- Develop and maintain the working network with authorities, assotiations and relevant organizations to carry out drug registration, cosmetic, medical device.
- Coordinate and provide regulatory guidance in pharma fields to the team, other functions and principals. Proactively analyse, comment and communicate any changes in the regulatory environment.
- Manage and support the Regulatory Affairs Team to ensure high quality of registration dossier and following with the local authority.
- Effectively manage and accelerate registration approvals.
- Develop, maintain and update the processes for product registration and license changes.
- Manage preparation, submission and follow of initial and renewal product registrations, variations.
- Review and approve labels in relation to regulatory compliance.
- Review and approve promotional material, submit/get the authority’s approval if needed.
- Coordinate, provide, review the registered product information on requirement of other functions like marketing, tender, demand, supply and importation.
- Manage the regulatory affairs staff when is assigned by RA Head
What Will Make You Successful:
- Bachelor's Degree in Pharmacy. At least 5 years of managerial/specialist experience in Regulatory Affairs for the Pharmaceutical industry
- Good relationship with the authorities related to registration tasks (Ministry of Health, Drug Administration of Vietnam)
- Good knowledge and understanding of legal requirements related to product registration for pharmaceutical products
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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