Work Schedule
Standard (Mon-Fri)Environmental Conditions
WarehouseJob Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Clinical Trial Services Site Korea as a part of Thermo Fisher Scientific is the world leader in clinical supply chain management and related support services. It has a worldwide network of packaging and distribution facilities.
Position Summary:
Lead Material Handler helps maintain all logistics, ensure efficient processes, and maximize the productivity of CTD Korea operations, under the direction of the Operations Leader. This includes distribution & receiving of clinical trial materials, return and destruction of pharmaceutical products, coordinating logistics processes, ensuring the quality of goods, and preparing related documents in compliance with cGMP. Also, this position oversees site Environment, Health, and Safety (EHS) management, including the provision of PPE, safety training, and ensuring compliance with PSG EHS standards and country-specific EHS regulations in Korea.
Responsibilities:
임상 시험용 의약품에 대한 입고, 출고, 반품, 폐기 관리 및 처리
창고 및 관련 문서작성 및 보관 관리
의약품 보관 및 출고에 필요한 포장재 관리
Shipper & Equipment Validation 계획수립 및 진행, 관리
현장 환경·보건·안전(EHS) 관리, 개인보호구(PPE) 지급, 안전 교육 실시, PSG EHS 표준운영절차(SOP) 및 국내(대한민국) 법규 준수 담당
PPI Business System & Operational Excellence
Facility 운영 업무 지원
Essential Duties
Receiving – 입고: 제품 보관 조건에 따른 입고 관리 및 입고 문서 관리
Receive, account and inspect all incoming shipments and deliveries.
Stage or store materials in the appropriate temperature conditions and warehouse locations.
Complete documentation and update computer systems appropriately and correctly.
Distribution – 출고: 제품, 온도계 출고 관리 및 출고 문서 관리
Process Pick Orders in a timely and accurate manner.
Package Clinical Trial Materials in the correct and appropriate shipping material.
Ensure the appropriate project instructions are followed.
Ensure the appropriate courier information is complete and available when presented to the couriers.
Export Shipment – QC check: 해외 배송 및 관련 문서 관리
Check the accuracy of picked drug supplies against client orders and ship distribution documents
Responsible for in-process check for Just-In-Time Labeling
Returns and Destruction – 반품 및 폐기: 수거된 제품의 검수, 보관, 폐기 관리
Receive and inspect all returned shipments and deliveries.
Retrieve and package all materials from inventory according to client instructions.
Arrange for appropriate transport and/or destruction of materials according to client instructions.
Complete documentation and update computer systems appropriately and correctly.
Liaise with customers/site/internal department on returns shipment arrangement
Generate monthly reports on returns shipment summary
Validation – 밸리데이션: Credo Shipper 및 Equipment Validation 계획 수립 및 진행, 관리
Prepares and executes validation protocols and writing reports for credo shippers
Prepares and executes Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) for equipment
Reviews/verifies data and performs statistical analysis
Supports special projects (as required)
Packaging Material – 포장재 관리: Credo 패널 및 Shipper 관리
Responsible for panel conditioning as per validation report
Responsible for stock management and procurement
Warehouse Inventory Data Management – 창고 입출고 및 리턴, 재고에 대한 데이터 관리
Responsible for warehouse inventory data integrity
Ensure physical inventory matches up with system inventory data
Support statutory performance reporting with area of responsibility
Reviews and analysis data to support management reporting
EHS Program Leadership & Ownership - 현장 환경·보건·안전(EHS) 관리
Own, lead, and continuously improve all site safety and health programs across manufacturing, laboratory, and office environments, including:
Employee safety programs and training
Chemical safety, dangerous goods handling, and laboratory safety programs
Ergonomics assessments, risk mitigation, and tracking
Emergency Response Team (ERT) preparedness, drills, and incident response
Incident investigation, root cause analysis, and corrective action management
Ensure EHS programs are effectively implemented, audited, and sustained in alignment with EHS Management System, EHS Standards, and applicable regulatory requirements.
Serve as the site subject matter expert for safety and health risks associated with chemical handling and high-risk operations.
Regulatory Compliance & Inspections
Waste Management & Vendor Oversight
Training, Engagement & Safety Culture
Emergency Preparedness & Business Continuity
NPI (New Product) assessment and documentation
Accountable for Change Control and SOP revision in accordance with requirements
Act as deputy of Operations Manager during his/her absence
Complete documentation and update computer systems appropriately and correctly. – 그 외 문서관리
PPI Business System & Operational Excellence
Facility management support
Qualifications:
Bachelor’s degree or equivalent experience
5+ years of experience in Warehousing operations or related area
SQL Knowledge, Data Analytics Skill
Working knowledge of Equipment & Shipper validation
Intermediate skills in MS office
영어 읽기, 쓰기, 말하기 중급 이상
병역필 또는 비대상자 선호
인천 지역 출퇴근 가능
지게차 자격증 보유 선호
Work Schedule:
08:00 AM to 17:00 PM core hours, additional hours as required.
보훈대상자 및 장애인 채용 안내
써모 피셔 사이언티픽 코리아는 다양성과 포용성을 바탕으로 모든 인재에게 공정한 기회를 제공하기 위해 노력하고 있습니다.
국가를 위해 헌신하신 보훈대상자 및 장애인 지원자분들을 적극 환영하며, 관련 법령에 따라 우대합니다.
온라인 지원 시, (3) 장애 여부(Disabled) 또는 (4) 보훈 대상(Veteran) 항목에 해당하시는 경우 ‘Yes’로 표시해 주시기 바랍니다.
또한, 지원 시 제출이 필요한 서류는 누락되지 않도록 반드시 안내 링크를 통해 확인해 주시기 바랍니다.