Role at a glance
- Job function
-
Manufacturing & Skilled Trades Quality Assurance & Quality Control
- Salary
- Not Disclosed
- Location
- Seoul, South Korea
- Work arrangement
- On-site
- Employment
- Full-time
- Education
- Bachelor's
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Qualifications
Required
- Minimum bachelor's degree (in Chemistry, Chemical Engineering, Life Science, Pharmaceutical Engineering, or related fields)
- Understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory and compendial (USP, EP, JP, etc.) requirements
- Good Interpersonal communication and Collaboration skills
- Demonstrated ability to organize and prioritize workload
Preferred
- Experience in pharmaceutical industry
- Experience in QC department
About the role
Original posting provided by 존슨앤드존슨(Johnson&Johnson)
About the role
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 Innovative Medicine and MedTech, 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.
What you'll do
• Complies with laboratory safety requirements
• Complies with laboratory related regulation and requirements
• Preparation/Revision and review of GMP/GLP documents (Test method documents, Lab notes (Worksheet), Procedures)
• Usage and Management of GMP document / Assure that GMP/GLP documents are properly maintained and/or archived
• Internal and external audit/inspection Preparation and Response
• Other laboratory Support activity (e.g., housekeeping)
• Perform QC testing in compliance with GMP and corporate requirements/procedures
• Review analytical data and test results
• Conduct and/or support laboratory investigations when issues occur
• Perform data integrity activities in accordance with applicable regulations and J&J requirements
• Utilize electronic systems (e.g., LIMS, MES, LES, Empower) for execution, review, and documentation of laboratory activities
• Laboratory system administration (LIMS, Empower, etc.)
• Lab equipment management (Qualification (Instrument Decommissioning included), Calibration, Maintenance, etc.)
• Coordinate/Document/Handling non-conformances, corrective actions (CAPAs) and changes (change control management)
• Manage and Review of GMP data in compliance with GMP and corporate requirements/Procedures
Requirements
• Minimum bachelor's degree (in Chemistry, Chemical Engineering, Life Science, Pharmaceutical Engineering, or related fields)
• Understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory and compendial (USP, EP, JP, etc.) requirements
• Good Interpersonal communication and Collaboration skills
• Demonstrated ability to organize and prioritize workload
Preferred qualifications
• Experience in pharmaceutical industry
• Experience in QC department
Benefits
자세한 사항은 홈페이지 참조
About the company
존슨앤드존슨(Johnson&Johnson)
Johnson & Johnson은 헬스케어 산업의 혁신을 선도하는 글로벌 회사로, 의료기기, 제약, 건강소비재 등 다양한 분야에서 제품과 서비스를 제공합니다. 환자, 의료진, 임직원, 지역사회, 주주를 최우선으로 생각하며 사업을 영위합니다. 의료 기술 사업부를 통해 혁신적인 의료기기를 개발하고 있으며, 제약 부문에서는 혁신 의약품 개발에 집중하고 있습니다. 국민의 건강과 삶의 질 향상에 기여하는 글로벌 헬스케어 기업입니다.