서울에서 최고의 quality specialist 채용공고 4개(지금 채용 중!)

Regulatory Affairs Specialist (Contract)
Zimmer Biomet —서울
- 임시직
Sr. Delivery Consultant - Connect, Professional Services
Amazon Web Services Korea LLC —서울
- 정규직
12일
Associate Mako Product Specialist 대구/경상
Stryker —서울 테헤란로
- 정규직
Associate Partner
McKinsey & Company —서울

More jobs to discover

Find similar jobs that you might be interested in.

Sr. Delivery Consultant - Connect, Professional Services
Amazon Web Services Korea LLC —서울
You will be required to travel to client locations and deliver professional services as needed. Experience leading or participating in customer-facing technical…
12일
Technical Sourcing Manager (관련 경력 15년 이상, 영어 가능자, 서울 근무)
Merck KGaA —서울
Procurement or Engineering working experience in multinational company related to Investment Projects sourcing in chemical, pharma or life science industry is…
5일

Show more similar jobs

서울의 quality specialist에 대한 최신 취업소식을 받고 싶습니다.

계정에 로그인하면 SimplyHired의 서비스 이용약관과 쿠키 및 개인정보 취급방침에 동의하는 것입니다.

더 많은 지역의 채용공고 둘러보기

quality specialist jobs near 서울

서울 지역 Product Specialist 채용공고

서울 지역 Operation Specialist 채용공고

서울특별시 지역 Product Manager Medical 채용공고

경기도 용인 지역 Regulatory Specialist 채용공고

서울 지역 Internal Communications Executive 채용공고

서울 지역 Quality Specialist 채용공고

서울 지역 Quality Assurance Specialist 채용공고

서울 지역 Implementation Consultant 채용공고

서울 지역 Aws Consultant 채용공고

Regulatory Affairs Specialist (Contract)

Zimmer Biomet -
서울

지금 지원하기

채용공고 세부정보

임시직 | 정규직

상세 직무 내용

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

Job Summary

This is a maternity leave replacement contract position with an expected contract duration from October 2026 to March 2028.

New product registration & Maintenance of existing product licenses
Compliance with MFDS & Corporate QA requirements

Principal Duties & Responsibilities

1. New product registration & Maintenance of existing product licenses (90%)

New product registration, Line-extension registration
Amendment of licenses, License renewal
Communicate and align with the global regulatory team to get support for local product registration and manage local regulatory systems and processes.
Documentation update for registration information (Update for; Registration master file, Sharepoint master file, Distribution registration folder, etc.)
Provide product registration status and results to the business team and related parties to help their plan and preparation in advance, work collaboratively with the business team, and identify and seek resolution of registration and quality issues for the operational effectiveness

2. Compliance with MFDS & Corporate QA requirements (10%)

KGMP maintenance e.g. on-site audit and document audit
Preparation of Korean labeling documents; Korean IFU & Korean label
Prepare/revise/control QM, PD, and SOP to ensure compliance with the Corporate and the MFDS requirements for Korean operation
Track and follow up on the new regulation/requirement (e.g. GMP, GSP, MDA, etc.)

Individual percentages should be greater than or equal to 5%.

This is not an exhaustive list of duties or functions and may not necessarily comprise all of the "essential functions" for purposes of the ADA.

Requirements

Expected Areas of Competence

Competent English language skills (reading, writing, listening, and fluent speaking)
Comprehensive knowledge of MFDS regulations
Strong writing and communication skills; ability to communicate effectively at multiple levels including with regulatory authorities
Knowledge of medical device products (Implants and/or electronic devices) and regulations and ability to interpret them
Ability to manage multiple projects
Responsible, professional, detail-oriented
Strong computer skills
Education/Experience Requirements

Bachelor’s Degree in life sciences, technical (engineering), or related field; advanced degree strongly preferred
3~7 years of experience required in Regulatory Affairs and/or Quality
Certifications an advantage including Regulatory Affairs (RAC), Quality Auditor, and NIDS RAC

Travel Expectations

No reason for disqualification for overseas travels

EOE/M/F/Vet/Disability

지금 지원하기

검색결과 새로고침

서울 지역 채용공고 quality specialist건

Regulatory Affairs Specialist (Contract)

Sr. Delivery Consultant - Connect, Professional Services

Associate Mako Product Specialist 대구/경상

Associate Partner

More jobs to discover

서울의 quality specialist에 대한 최신 취업소식을 받고 싶습니다.

더 많은 지역의 채용공고 둘러보기

Job Summary

Principal Duties & Responsibilities

Requirements

Travel Expectations

구직자 도구

기업회원 도구

찾아보기

연결 상태 유지하기