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Regulatory Affairs Associate ¸ðÁý

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   - Register BP/Pharma products and maintain the regulatory license through full understanding

      of the relevant regulations/SOPs and the best registration strategy

   - Monitor regulatory environment routinely and implement in a timely manner or spread out to the responsible

      & relevant dept not to have any business impact to BHP Korea if necessary.

   - Review the product labeling and package materials for any violation or possible issue before

      they are delivered to customer.

   - Harmonize Korean product labels with global and prompt notice to HQ about local status for labeling

      implementation to avoid any local issue.

   - Support the clinical trial of new drug with local and global strategy

   - Comply with pharmaceutical regulations and BHC ethical business practices, with full understanding

      of the code of conducts while ensuring complete compliance of marketing activities



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   1) Education:

      - Minimum 4-Year University graduate- Pharmacist/Biologist or Chemist preferred

   2) Personal Specification:

      - knowledge of regulations and its requirements is preferred.

      - Ability to produce qualified applications

      - Ability to communicate effectively with health authority

      - Good command of English in writing and speaking

      - Good understanding of natural and pharmaceutical science



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