Qm Officer - Quality Management Officer
Hạn nộp hồ sơ:
04/07/2026
•
Ứng tuyển sớm để được ưu tiên!
Mô tả công việc
Product quality management
- Check COAs and product label artworks prior to importation, ensuring all information complies with legal regulations and approved product dossiers.
- Inspect product quality upon warehousing, customer returns, or when incidents arise during operations. Coordinate with relevant departments or manufacturers to resolve any arising issues.
- Manage secondary labeling activities, including managing and updating secondary label information based on approved templates, ordering label printing, supervising and coordinating labeling activities, and reviewing secondary labeling batch records.
- Monitor product quality trends and report any abnormalities to management.
- Monitor shipment temperature data during transportation.
- Inspect and supervise product destruction.
- Prepare periodic reports for special controlled drugs.
Quality management system
- Draft, review, and revise SOPs in accordance with current regulations. Monitor SOP compliance across relevant departments. Control, issue, and archive assigned documents and records.
- Perform temperature mapping for warehouses (ambient and cold storage), transport vehicles, and cold storage boxes. Monitor the data logger calibration schedule.
- Prepare documentation for and host external audits/inspections (GSP, GDP, customer audits, ETC.) within assigned responsibilities. Support the implementation of CAPA plans.
- Prepare periodic reports on the quality management system.
- Support the coordination and supervision of Change Control implementation.
- Support the evaluation and quality monitoring of suppliers.
- Perform other tasks as required.
Yêu cầu công việc
- Good command of English, particularly in reading and writing skills; candidates with strong listening and speaking skills are highly preferred.
- Careful, meticulous, and highly accurate.
- Strong self-learning capability.
- University graduated majoring in Pharmacy
- At least 2 years of experience in QA/QC within the pharmaceutical industry (manufacturing, warehousing, or import & distribution environment) ---
- Foundational knowledge of GMP, GSP, GDP, along with an understanding of medicine import regulations.
- Proactive, responsible, structured.
- Clear and effective communication skills.
- Training and presentation skills.
- Proficient in office computing (Minimum Microsoft Office: Word, Excel, PowerPoint, Teams, Outlook); candidates with the ability to apply AI tools are preferred.
Quyền lợi
- Competitive compensation package.
- Full social insurance contribution based on gross salary.
- Premium health insurance coverage.
- Well-being programs supporting physical, mental, and personal development.
- Dynamic, collaborative, and growth-oriented working environment.
- 24/7 accident insurance and annual health check-ups.
- Clear long-service recognition policy with strong career advancement opportunities.
Thông tin chung
Ngày đăng
10/06/2026
Cấp bậc
Nhân viên
Số lượng tuyển
1
Hình thức làm việc
Toàn thời gian cố định
Yêu cầu kinh nghiệm
2 năm
Địa điểm làm việc
TP.HCM:Lô IV-13, đường số 2, KCN Tân Bình, Tân Phú
Công Ty TNHH Mega Lifesciences (Việt Nam)
Địa chỉ:Tòa nhà E-Town, Số 364, Đường Cộng Hòa, Phường Tân Bình, TP Hồ Chí Minh (Quận Tân Bình Cũ)
Quy mô:Trên 300 nhân viên
Xem trang công ty

