[ 담당업무 ]

• - Develop and implement regulatory plans for new products and license maintenance in line with business strategy.
  - Monitor regulatory requirements and ensure compliance with internal and external standards.
  - Review promotional materials, SOPs, and documentation for regulatory compliance.
  - Manage local labeling content per regulations and internal SOPs.
  - Participate in regional project teams as needed.
• 
  

[ 자격조건 ]

- 8–12 years of experience in Medical Device, Pharmaceutical company
- Pharmacist (preferred)
- ​Fluent in English

[ 전형방법 ]

1차 서류전형 /2차 면접전형

[ 제출서류 ] 

국문.영문이력서.경력기술서 포함 (각종 증빙서류는 서류전형합격자에 한해 추후제출) 

이메일: carly.lee@peoplework.co.kr******@*******.*** 

채용담당 : 이경아 전무 ( ***-****-****/ ***-****-****)

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