핵심 정보
- 경력
- 경력 8년 ↑
- 학력
- 대졸(4년제) 이상
- 근무형태
- 정규직
- 급여
- 면접 후 결정
- 근무지역
- 서울 용산구
본 채용정보는 마감되었습니다.
한국존슨앤드존슨메디칼(주)에서 채용공고가 시작되면 이메일로 알려드립니다.
상세요강
About Johnson & Johnson
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/.
- 포지션: RA Manager
- 계열사: 존슨앤드존슨 메드테크 (MedTech)
- 근무지: 서울시 용산구
- 근무 형태: Regular
[Summary]
Manages
submission of new product applications to the regulatory agencies. Directs and
coordinates activities concerned with the submission and approval products to
government regulatory agencies. Provides guidance to project team members
regarding regulatory compliance issues. Oversees the preparation and
maintenance of regulatory submissions and files. Ensures adherence to standard
operating procedures and protocol for the rapid and timely approval of new
products and regulatory support of marketed products and other products.
Interacts with regulatory agency personnel in order to expedite approval of
pending application and to resolve regulatory matters. Consults with management
personal to establish strategies and prepare appropriate regulatory filings for
the regulatory activities. In general, has responsibility for projects of
medium and large scope, such as accountability for
regional/global/multi-functional projects.
[Responsibilities]
Functional
and Technical Competencies:
-
Leverages deep knowledge of the regulatory environment, including compliance,
current and proposed laws, regulations and guidance, to develop and oversee the
execution of compliant Regulatory strategies that are aligned with business
objectives of the company.
-
Leverages a deep scientific and technical understanding of products (medical
devices, biologics or pharmaceuticals).
-
Encourages and leads others to find ways to continuously improve, learn about
new scientific, technological and Regulatory developments, develop new capabilities,
and learn from past challenges and experience in order to proactively adapt to
change and drive innovative thinking.
Manages
projects within timeline and budget requirements by acquiring and coordinating
needed resources.
-
Leverages in-depth knowledge of the sector, organizational vision, Regulatory
Affairs function, and cross-functional business partners to make informed
business decisions and create and execute business strategies.
-
Leverages knowledge of the healthcare environment and external marketplace
Leadership
Competencies:
-
Guides others in defining and prioritizing key decision criteria, considering
the benefits and risks of alternatives, Credo, and evaluating immediate and
future implications when making business level decisions.
-
Quickly and effectively prioritizes critical Regulatory Affairs goals/
initiatives and manages resources in difficult, complex, or crisis situations.
-
Manages change by creating structure and providing clear direction when facing
ambiguity and uncertainty.
-
Understands others’ motivations, needs, and concerns even when they are
difficult to discern and applies understanding to establish trust and
credibility and influence others.
-
Creates compelling negotiating positions that build support and consensus among
key stakeholders. Challenges the positions of others to reach win-win outcomes.
-
Mentors others in using verbal communication that are convincing, engaging, and
articulate and translate complex information into key facts and rational
arguments that are influential, meaningful, and actionable.
-
Fully engages others by asking incisive and provoking questions, always
ensuring mutual understanding, particularly when encountering conflicting
opinions.
[Requirements]
-
8+ years Regulatory Affairs or related field, Medical Device experience
-
Experienced in dealing product registration, registration maintenance and KGMP
in medical device product categories
-
Experienced in developing team and leading team project
-
Excellent communication and strong interpersonal skills
-
Ability to collaborate with cross-functional partners/teams
-
Strong project management skills
-
Well defined problem solving
-
Strong sensitivity for dynamic and multi-cultural environments
-
Experienced in driving industry projects as a lead
-
Experience with international regulations
-
Proven analytical abilities
-
Fluent in both verbal and written English and Korean
[지원
방법]
www.careers.jnj.com 접속
-> Position Number 2406172891W 검색 -> 해당
모집
공고의
“Apply Now” 클릭
후
온라인
지원
프로세스
진행
[제출
서류]
국&영문
자유
양식의
이력서/자기소개서
[서류
마감일]
채용시
마감
[For
more Johnson & Johnson]
-
J&J Careers 유튜브 채널 : https://www.youtube.com/channel/UCZEsWOZwbcjcXHrgYq7sP4Q
-
J&J Korea Facebook: https://www.facebook.com/JNJCareersKorea/
-
J&J Linkedin: https://www.linkedin.com/company/johnson-&-johnson/
-
J&J Corporate Page: http://www.jobkorea.co.kr/Company/1605233/Info
[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.
복리후생
- 지원금/보험
- 건강검진, 의료비지원(본인), 각종 경조사 지원, 의료비지원(가족), 헬스비 지급, 자...
- 급여제도
- 퇴직연금, 장기근속자 포상, 성과급, 가족수당, 4대 보험
- 선물
- 명절선물/귀향비
- 교육/생활
- 사내동호회 운영
- 조직문화
- 캐주얼데이
- 리프레시
- 연차, 경조휴가제, 휴가비지원, 육아휴직, 남성출산휴가
기업정보
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- 업종
- 의료용품 도매업
- 설립일
- 1988년 12월 22일 (업력 37년차)
- 매출액
- 3,011억 2,614만원 (2023년 기준)
- 홈페이지
- www.jnjmed.co.kr
- 기업주소
- 서울 용산구 한강대로 92
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