QA Specialist (Pharma)
Mô tả công việc
- JOB PURPOSE : Perform and monitor tasks related to the system aspect of QA department; support other tasks of QA department to ensure all processes and products reach GMP and group requirements, which are defined in global documents and guidelines.
- KEY ACCOUNTABILITIES: 1.Self-Inspection & audit/ inspection
- Develop and execute self-inspection plans for GMP & Halal in accordance with company procedures.
- Lead regulatory inspection preparation and inspection: Global Quality Audit, GMP inspection by DAV, TGA, GMP for cosmetics by DAV, Halal by LPOM MUI, HS…, Track and follow up on corrective and preventive actions (CAPA).
- Lead GMP guidance assessments and Implementation Follow-up. 2.Quality System Management
- Quality Performance Monitoring
- Lead QMI (Quality Management Indicators) and QCMA (Quality Control Maturity Assessment) programs
- Monitor, summarize, and report results to managers
- Lead the Directive implementation program at site
- Ensure compliance between internal procedures and global quality documents 3.Others
- Take the Local Admin role for CMS system and back up Local Admin for Event, CAPA, ILI (Investigation & Learning from Incidents), and Change Control (CC) systems
- Support the implementation of quality improvement initiatives within the site
- Ensure that a timely and effective communication and escalation process exists to raise quality issues to the appropriate levels of management
- Support other activities when needed
- Compliance with HSE requirements
Yêu cầu ứng viên
- Graduated from a university with a major in
- Pharmacy, Chemistry, or a related field .
- At least 6 months experience and used to work in quality assurance systems or GMP sites
- Organized, planning and time management
- Two-way communication, adaptability to multi-culture environment.
- Fluent English - 4 skills
- Using Word, Excel, Power Point
Thông tin tham khảo
- Thị trường tại Hồ Chí Minh
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- Nguồn tin
- Nguồn: CareerViet · đăng 04/11/2026
