RA (Regulatory Affairs)
- Company
- 대기업계열제약회사
- Position
- RA (Regulatory Affairs)
- Status
- CLOSE
대기업 계열 제약회사에서 다음과 같이 “Sr. RA (Regulatory Affairs)” 인재를 찾습니다.
* Job Title : Sr. RA
* Position : Kwajang ~ Chajang
* Age: Born after 1970
* Gender : Male or Female
* Location : Seoul
[RESPONSIBILITIES]
- Responsible for Regulatory Affairs duties for new product registration
- Ensure company meets regulatory and statutory requirements of government in doing business of Pharmaceutical
- Closely monitor the future change of regulation of healthcare industry through keeping the updated information
- Provide leadership to RA team to do daily work most effectively through coaching and training
- Communicate and collaborate with Regional/Corporate RA Team effectively for the timely launch of new products
- Share expertise with marketing personnel to develop strategic planning to manage the reimbursement price in order to secure the optimum level of company profit
- Ensure product data file and documents are well maintained
- Manage product complaints to enhance company reputation and better customer services
- Strongly involve in new product development and introduction suitable for Korean Market through constant market research
- Build good relationship with Korean 3rd parties (Distributors) and Patient Advocacy Group and Social Community
- Responsible for Regulatory Affairs duties for new product registration
- Ensure company meets regulatory and statutory requirements of government in doing business of Pharmaceutical
- Closely monitor the future change of regulation of healthcare industry through keeping the updated information
- Provide leadership to RA team to do daily work most effectively through coaching and training
- Communicate and collaborate with Regional/Corporate RA Team effectively for the timely launch of new products
- Share expertise with marketing personnel to develop strategic planning to manage the reimbursement price in order to secure the optimum level of company profit
- Ensure product data file and documents are well maintained
- Manage product complaints to enhance company reputation and better customer services
- Strongly involve in new product development and introduction suitable for Korean Market through constant market research
- Build good relationship with Korean 3rd parties (Distributors) and Patient Advocacy Group and Social Community
* 개발부서 내 팀원 관리
* 허가 및 등록 업무 총괄
* 대관업무 총괄
* 허가 및 등록 업무 총괄
* 대관업무 총괄
[QUALIFICATIONS]
- Pharmacist preferred
- Over 5 years experience in RA
- Aggressive and open mind character & PC Proficiency
- Good relationship with co-workers and relevant 3rd parties
- 국내제약회사의 허가, 등록부 또는 개발부서 경력자
- 식약청 대관 업무 경험자 선호
Those who are interested in this opportunity, please submit your Resume in MS Word Format by email urgently. Only qualified candidates will be contacted for interview. All resumes not contacted will be kept in DB confidentially for future positions.
Kyung Jin KIM
CEO & Executive Search Consultant
Exdigm Inc.
Phone: 070-8260-3646
Mobile: 010-8722-1272
Email: ceo@exdigm.com exdigm@naver.com
CEO & Executive Search Consultant
Exdigm Inc.
Phone: 070-8260-3646
Mobile: 010-8722-1272
Email: ceo@exdigm.com exdigm@naver.com