Regulatory Affairs Assistant, Chemicals and Product Safety

Knoell
서울
1일 전

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

  • Coordinate and manage a variety of projects with general supervision, to be in compliance with national regulatory requirements.
  • Assistance in management of larger scale and long-term projects.
  • Preparation of administrative paperwork for regulatory compliance.
  • Communication and close collaboration with clients to manage projects related to dossier creation and submission, and to respond client inquiries regarding regulatory matters.
YOUR PROFILE
  • University degree (at least bachelor’s degree)
  • Good language skills both in English and Korean (spoken and written); additional language skills would be an asset.
  • Professional work experience as project manager
  • Strong communication skills in, verbal and written with adequate social skills
  • Self-disciplined, capable of excellent time management, prioritization, and multitasking in a fast-paced environment
  • Strong problem-solving skills and logical thinking
  • Working with others as a team
  • Attention to detail
  • Proactive attitude and mind
  • 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 and is a remote-first company, where you have the flexibility to work from home, at our headquarters in Mannheim or at one of our local offices based in your location.
  • 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.
  • At knoell we have a global employee referral program as part of the recruitment process where you can actively participate and get rewarded for referring talent to knoell.

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!

Apply
Other Job Recommendations:

Regulatory Affairs Specialist

Novartis
Seoul
  • To set registration plan, to perform product registration in...
  • Review new projects and aset development plan (timeline...
6일 전

Associate Regulatory Affairs Specialist

Medtronic
서울
  • Directs or performs coordination and preparation of document...
  • Keeps abreast of regulatory procedures and changes. ...
4주 전

대전 바이오 공장 신설 - Chemical Safety Specialist (화학 물질&대기환경, 3년 이상)

Merck KGaA
서울
  • Compliance of Safety Control of Dangerous Substance Act...
  • Management and compliance of global standard and guidelines...
1일 전

Senior Clinical Regulatory and Start Up Specialist

Precision Medicine Group
서울
  • Preparation of Clinical Trial Application Forms as well as...
  • Preparation of Clinical Trial Application Forms as well as...
1주 전

Sr Specialist, Regulatory Affairs

Baxter
서울
  • Develop and execute regulatory plans for complex projects...
  • Ensure project teams and business objectives and...
2일 전

Manager or Senior Manager, Regulatory Affairs, Korea

BeOne Medicines
서울
  • Manage and oversee all relevant maintenance activities...
  • Collaborate and communicate effectively with teams...
3주 전

Product Manager - Korea

Umami Bioworks
서울
At Umami Bioworks, we are a leading bioplatform for the development and production of sustainable planetary biosolutions Through...
2주 전

Product Manager II (Ads Product)

Coupang
Seoul
  • Product Management 경험 3년 이상 보유한 분
  • 반복주기가 짧은 Agile 환경에서 Product Iteration 실무 경험을 보유한 분
  • Product Management 경험 5년 이상 보유한 분
4주 전

Principal, Brand Management (HPC)

Coupang
Seoul
  • 목표(성장과 혁신)에 대해 비전을 제시하며 실행할 수 있는 분 
  • 변화에 대해 두려움이 없고, 도전할 수 있는 분
  • 전형절차는 직무별로 다르게 운영될 수 있으며, 일정 및 상황에 따라 변동될 수 있습니다...
1일 전

R&D Manager - Synthesis (PhD, Precursors/Organic, 사택 지원)

Merck KGaA
서울
  • Stay up-to-date with the latest advancements in...
  • <유의사항>여러분이 찾고 계시는 채용 포지션이 없으신가요? 그렇다면 인재풀(클릭))에 여러분의...
1일 전