[Bayer CropScience] Regulatory Affairs Manager

[ES 사업부 분사 안내]

You are applying for a position in Bayer’s Environmental Science business. Bayer intends to divest this business to Cinven in 2022. Cinven is an international investment firm focused on building world-class global companies & will enable ES to advance towards our vision of healthy environments for everyone, everywhere. 

With joining Environmental Science, you will be joining a global industry leader in its markets, with the opportunity to be part of forming a new company in an agile, entrepreneurial and passionate team.

We encourage you to discover more about our activities by watching the ES Dare to Explore video:

https://www.youtube.com/watch?v=ugzJ5LIhG5o 

[R&R]

1. BS registration

: Handle the BS registration of Professional Pest Management & Vector control - Handle whole process for Registration affair under MOE for the BS of current Professional Pest Management & Vector control products.

Contact to MOE and its sub-organizations for Registration & other related matters to ensure full compliance of local law & regulation. Monitor/Update related regulatory guidelines.

2. White registration

: Handle the AIs & products re-/registration of Professional Pest Management & Vector control - Handle whole process for Registration affair under MOE for current Professional Pest Management & Vector control products and New products via PMC.

Contact to MOE and its sub-organizations for Registration & other related matters to ensure full compliance of local law & regulation. Monitor/Update related regulatory guidelines.

3. Green products registration

: Handle the products re-/registration of Agrochemicals - Handle whole process for Registration affair under RDA for Turf and Ornamental, Forestry and IVM.

Contact to RDA and its sub-organizations for Registration & other related matters to ensure full compliance of local law & regulation.

Monitor/Update related regulatory guidelines.

4. Quality Management

: Handle to fulfill the local requirements for the product quality of ES portfolio and ensure to align with product stewardship. (Shelf life management, import support, Product Quality, and stock inspection to comply with Bayer and local regulation).

Generate/Modify labelling text for new and existing products in all segments to comply with Bayer and local regulation.

5. Stakeholder Engagement

: Engage external stakeholders such as regulatory authorities, leading universities, research center & associations to ensure trial results, and registration dossier will be accepted by RDA & MOE.

[Qualifications / Requirement]

1. Ability to analyze technical data and understand fully the requirements of the regulatory authorities in Korea

2. Extensive knowledge on Act on Registration, Evaluation, etc. of Chemicals

3. Effective interpersonal skills for interfacing with other Bayer, university, regulatory department, association and customer personnel.

4. Prefer Experience on Registration of Chemical at least 5 years.

5. Prefer Excellent English skill.