[MedTech] RA Specialist SPECIAL PROJECTS - 2406191129W

Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in pharmaceutical, medical devices and diagnostics markets, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/ .

1. 포지션: Regulatory Affairs Specialist – Special Projects

2. 계열사: 존슨앤드존슨 메드테크 (MedTech)

3. 근무지: 서울시 용산구

4. 근무 형태: Fixed Term(1 year)

[Responsibilities]

1. Takes charge in products for assigned projects.

2. Prepares and submits required regulatory applications for new products for replacement, change of manufacturing process

3. Monitors and submits regulatory applications for changes of approved products

4. Interacts with regulatory agency personnel in order to expedite approval of pending applications and to resolve regulatory matters

5. Communicates information and presents status updates on product/project activities to key internal/external stakeholders when requested.

6. Follows up of mandatory requirements for registration: local certificates, importation of samples and local testing, etc.

7. Researches and consolidates regulatory requirements and communicate their information with supervisor and manager.

8. Supports the RA team in projects.

9. Supports in the development of best practices for Regulatory Affairs processes.

10. Conforms regulatory compliance.

11. The incumbent must have the ability to work effectively and process requests/work within required timeframes.

12. A team player with a diligent and sincere attitude and mindset

13. Has a strong sense of responsibility on meeting due/target and quality/integrity/accuracy of the output

14. Views new and ambiguous challenges as a learning opportunity

[Requirements]

• A minimum Bachelor’s degree is required.

• Minimum 3 years of progressive RA experience in HealthCare industry is preferred.

• Knowledge of regulatory environment, relative law and regulations on Medical Devices.

• Understanding of regulatory requirements.

• Prefer holding a Regulatory Affairs Certification (RAC)

• Experts in MS Word, Excel, Power Point and HWP etc.

• Good at writing and translation skill in English

• Less than 10% travel (oversea and domestic)

[지원 방법]

www.careers.jnj.com 접속 -> Position Number 2406191129W 검색 -> 해당 모집 공고의 “Apply Now” 클릭 후 온라인 지원 프로세스 진행

[제출 서류]

국&영문 자유 양식의 이력서/자기소개서

[서류 마감일]

채용시 마감

[유의사항]

• 국가 보훈 대상자 및 장애인은 관련 서류 제출 시 관계 법령에 의거하여 우대합니다.

• 서류 전형 합격자에 한하여 개별 통보합니다. 단, 회사 사정에 따라 지연될 수 있습니다.

• 입사 지원 서류에 허위 사실이 발견될 경우, 채용 확정 이후라도 채용이 취소될 수 있으며 향후 채용이 제한됩니다.

• 제출된 서류는 반환되지 않으며, 별도 요청 시 삭제합니다.

Qualifications

See above

Primary Location Asia Pacific-South Korea-Seoul-Yongsan-gu

Organization Johnson & Johnson Medical Korea (Ltd.) (7225)

Job Function Project/Program Management

Req ID: 2406191129W