핵심 정보
- 경력
- 경력 7년 ↑
- 학력
- 대졸(4년제) 이상
- 근무형태
- 정규직
- 급여
- 면접 후 결정
- 근무지역
- 서울 강남구
본 채용정보는 마감되었습니다.
(주)플러스휴먼리소스에서 채용공고가 시작되면 이메일로 알려드립니다.
상세요강
▣ 채용 포지션 : 제약사업부 Sr. RA Specialist
-Registering new products and managing existing products by leveraging a current and changing regulatory environment.
-Liaising, responding to, and negotiating with regulatory authorities.
-Support business planning activities by providing of smart registration strategy.
-Compliant with the current ** procedure.
-Leading regulatory compliance management.
-Achieve registration approval for planned new products and ensure subsequent maintenance of existing drugs on time.
-Provide the best registration strategy and timeline and communicate it with stakeholders.
-Secure product license maintenance according to local regulations and global ** compliance standards.
-Understand the regulatory environment changes and prepare for the implementation in compliance with the new regulation and ** procedures.
-Provide proper and exact Regulatory related information to stakeholders.
-Maintain well-managed external communication with related Health Authorities.
-Review registration requirements upon request by internal stakeholders.
-Leading regulatory compliance management: regular monitoring & implementing actions for RA systems as trainer level. Analyzing regulations and environment, and keeping stakeholders updated.
-Product/Business license registration, maintenance, and relevant regulatory activities for Pharmaceutical Products (chemical & biologics).
-Communication with the global and local stakeholders regarding the RA topics.
-Promotional material review for the assigned products.
-Compliance with the **procedures, performing the related activities.
- 대졸이상 (약학 우대 / 관련전공 선호 )
- 다국적기업 경력자 선호
- 제약사업 RA 7년이상 ~
- 영어 상급
▣ 전형방법 : 서류전형>면접(1차실무/2차임원)>OFFER협의>최종결과발표
▣ 제출서류 : 영문(필수) 이력서 및 경력중심 자기소개서 (MS워드 형식)
▣ 제출방법 : ymlim@plus-hr.co.kr 로 이메일 접수
-. 최종연봉, 희망연봉 필히 기재
-. 첨부 표준이력서양식 사용 권장
-Registering new products and managing existing products by leveraging a current and changing regulatory environment.
-Liaising, responding to, and negotiating with regulatory authorities.
-Support business planning activities by providing of smart registration strategy.
-Compliant with the current ** procedure.
-Leading regulatory compliance management.
-Achieve registration approval for planned new products and ensure subsequent maintenance of existing drugs on time.
-Provide the best registration strategy and timeline and communicate it with stakeholders.
-Secure product license maintenance according to local regulations and global ** compliance standards.
-Understand the regulatory environment changes and prepare for the implementation in compliance with the new regulation and ** procedures.
-Provide proper and exact Regulatory related information to stakeholders.
-Maintain well-managed external communication with related Health Authorities.
-Review registration requirements upon request by internal stakeholders.
-Leading regulatory compliance management: regular monitoring & implementing actions for RA systems as trainer level. Analyzing regulations and environment, and keeping stakeholders updated.
-Product/Business license registration, maintenance, and relevant regulatory activities for Pharmaceutical Products (chemical & biologics).
-Communication with the global and local stakeholders regarding the RA topics.
-Promotional material review for the assigned products.
-Compliance with the **procedures, performing the related activities.
- 대졸이상 (약학 우대 / 관련전공 선호 )
- 다국적기업 경력자 선호
- 제약사업 RA 7년이상 ~
- 영어 상급
▣ 전형방법 : 서류전형>면접(1차실무/2차임원)>OFFER협의>최종결과발표
▣ 제출서류 : 영문(필수) 이력서 및 경력중심 자기소개서 (MS워드 형식)
▣ 제출방법 : ymlim@plus-hr.co.kr 로 이메일 접수
-. 최종연봉, 희망연봉 필히 기재
-. 첨부 표준이력서양식 사용 권장
함께하기 위한 방법
- 접수기간 : 2024년 06월 27일 (목)10시 00분 ~ 2024년 07월 12일 (금) 23시 59분
- 접수방법 : 사람인 입사지원
- 이력서양식 : 사람인 이력서 양식
함께하기 위한 여정
- 서류전형
- 1차면접
- 최종합격
이어보는 Ai매치 채용정보
사람인 인공지능 기술 기반으로 맞춤 공고를 추천해드리는 사람인의 채용정보제공 서비스입니다.
사람인 인공지능 기술 기반으로 맞춤 공고를 추천해드리는 사람인의 채용정보제공 서비스입니다.