TO Process science assistant (Fixed term)
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- Posting Date:
- End Date:
- Job ID:
- 2607043949W
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What we do
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.
Who We Are
Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.
Role reports to:
Manager, Process ScienceLocation:
Asia Pacific, South Korea, Chungcheongbuk-do, CheongjuWork Location:
Fully OnsiteWhat you will do
The TO Process science assistant will support activities related to process development for new products, technical manufacturing support, technology transfer projects, process optimization, and productivity initiatives. This role also involves troubleshooting, investigations, and life cycle management, ensuring compliance with Kenvue procedures, regulatory requirements, GMP, EHS&S, and corporate quality standards.
Key Responsibilities
Process Development & Technology Transfer
- Prepare Laboratory Batch raw materials, and batch sheet.
- Conduct laboratory batch studies, scale-up trials, and stability testing.
- Prepare technical documentation to support product launches and reformulations.
- Sample of the Raw materials, bulk and finished goods and coordinate shipping to other
Lab management
- Lead lab maintenance, daily verification, calibration for lab equipment.
- Housekeeping for TO laboratory.
Validation
- Prepare validation protocol/report for mixing, filling, and cleaning processes.
- Ensure all validation activities comply with international and local regulatory requirements, GMP, EHS&S, and corporate quality standards.
Cost Improvement Projects (CIP)
- Execute cost improvement projects (CIP) to enhance productivity and reduce cycle time.
- Manage Raw material Phase in Phase out for CIP and BCP.
- Support to eliminate non-value-added activities and drive process optimization through technology innovation.
- Collaborate with cross-functional teams to implement sustainable improvements.
Investigations & CAPA
- Support investigation for resolving process deviations, non-conformances, and operational issues.
- Support root cause analysis and implement corrective and preventive actions (CAPA)
What we are looking for
- Bachelor’s degree in Chemistry, Chemical Engineering, or related scientific discipline.
- good communication skills in both Korean and English.
- Proven ability to collaborate within cross-functional teams.
- Proactive, innovative mindset with a willingness to challenge conventional approaches.
- Strong owner mind set to ensure deliverable to be completed on time.
(국문)
포지션 소개
Technical Operation Process Science Assistant는 신제품 공정 개발, 제조 기술 지원, 기술 이전(Tech Transfer) 및 공정 개선 활동을 실험실 및 현장 중심으로 지원하는 역할입니다.
제조·개발에서의 실무 경험을 쌓고, GMP 기반 공정, Validation, 원가 절감 프로젝트(CIP)에 직접 참여할 수 있는 기회가 제공됩니다.
주요 업무
공정 개발 및 기술 지원
- 실험실 배치 수행을 위한 원료 준비 및 Batch Sheet 작성 지원
- 실험실 배치 시험, Scale-up Trial 및 안정성 시험 수행 지원
- 신제품 출시 및 리포뮬레이션 관련 기술 문서 작성 지원
- 원료, 벌크, 완제품 샘플링 및 타 실험실/사이트로의 배송 지원
실험실 운영 관리
- 실험실 장비의 일상 점검, 유지보수 및 교정(Calibration) 관리 지원
- TO 실험실 하우스키핑 및 안전·품질 기준 준수
Validation 및 프로젝트 지원
- Mixing, Filling, Cleaning 공정에 대한 Validation 문서 작성 지원
- 원가 절감 및 생산성 향상 프로젝트(CIP) 실행 지원
- 원료 Phase-in / Phase-out 관리 및 유관 부서 협업 지원
조사 및 개선 활동
- 공정 이상, 일탈(Deviation), 부적합 사항에 대한 조사 활동 지원
- Root Cause Analysis 및 시정·예방조치(CAPA) 실행 지원
이런 분을 찾습니다
필수 요건
- 화학, 화학공학 또는 관련 이공계 전공 학사 이상
- 한국어 및 영어 기본 커뮤니케이션 가능자
- 책임감 있고 꼼꼼한 업무 수행 능력
- 팀 내 협업 및 현장 업무에 대한 적극적인 태도
우대 사항
- GMP 환경 또는 제조/실험실 근무 경험
- 화장품, 의약외품, 소비재(FMCG) 관련 경험
- Validation, 공정 개발, Tech Transfer 관련 경험
- MS Office 및 문서 작성 능력
- 글로벌 회사에서 제조/혁신에 대한 실무 경험을 쌓고 싶은 분
- 공정과 품질에 대한 이해를 바탕으로 성장하고 싶은 분
- 주어진 업무를 끝까지 책임감 있게 수행하는 분
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