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Regulatory Affairs Manager, Biocides (f\m\d) at knoell | softgarden View job here Regulatory Affairs Manager, Biocides (f\m\d)

• Full Time
• Seoul, South Korea
• With Professional Experience
• 1/30/26

Contact person

Hafsa Shakil Working Student Recruitment Coordination

Join Us in Shaping the Future of Regulatory Services.

knoell is one of the leading global service providers in regulatory registration, clinical development, and product development support. As a family-owned business, we take pride in our commitment to the highest standards and believe that people are at the heart of our success. With our team of scientific and regulatory experts and an extensive network of partners, we ensure reliable solutions that address our clients' global business needs right from the start.

At knoell, we are guided by our core values of commitment, reliability, excellence and diversity. Are you someone who thrives in a collaborative environment? Do you take pride in delivering high-quality results and upholding excellence in everything you do? At knoell, we are passionate about embracing diverse perspectives, knowing that this fuels innovation and strengthens our impact. If you're ready to be part of a team that values these principles, we want to hear from you!

Think Globally. Act Locally.

YOUR ROLE

Regulatory Affairs Manager is responsible for project coordination and management of a variety of regulatory activities within regulatory affairs. It includes communication and close local and global co-operation with our clients, authorities, knoell partners, and knoell colleagues. This person also monitors and shares new regulatory developments in certain areas.

• Coordinate and manage a variety of projects independently within regulatory affairs, using your communication and organizational skills.
• Oversee the registration of biocidal products and active substances in compliance with national and international regulatory requirements, e.g. the Korean biocides regulation (K-BPR, Consumer Chemical Products and Biocides Safety Act) or EU Biocidal Products Regulation.
• Communicate and closely collaborate with clients to manage projects related to dossier creation and submission, and respond to client enquiries regarding regulatory matters.
• Develop advanced regulatory strategies for our clients together with technical experts.
• Support our clients by facilitating their communication with authorities in terms of regulatory compliance.
• Monitor and share new regulatory developments in certain areas

YOUR PROFILE

• Education and training: University degree (at least bachelor’s degree)
• Professional work experience as project manager
• Good language skills both in English and Korean (spoken and written); additional language skills would be an asset.
• Strong communication skills in, verbal and written form with adequate social skills
• Programming Experience (AI & Software)
• Minimum 3-5 years of experience in regulatory affairs, following areas preferred: BPR, chemical regulatory affairs, EHS
• Strong problem solving skills and logical thinking
• Proactive attitude and mind
• Attention to detail
• Time management skills
• Working with others as a team
• Professional work experience in an international company/organization preferred

WHAT WE OFFER

• Work in a dynamic family-owned business environment with an international team in which new ideas, creative approaches, and collaboration are valued.
• You will have the opportunity to work with market leaders in our industry.
• Development is core, and at knoell we offer various opportunities to support your personal, leadership and technical development, including English language courses to help you effectively communicate in our business language.
• knoell offers a flexible working policy, where you have the flexibility to work from home.
• Part-time work options are generally supported on request subject to meeting business requirements.
• It is important to us that you have both a career and personal life – we celebrate the work-life balance of our colleagues.

If you have any questions, feel free to reach out to us at application@knoell.com. If you're looking to join a global leader in regulatory and clinical services, where you can make a real impact and contribute to a team that values your contributions, then knoell is the place for you.

We look forward to receiving your application!

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