Responsibilities
- To ensure that all quality control activities and other assigned jobs are performed in conformance to the GMP standards.
- To perform method development & validation and other quality control activities.
- Draft, review and revise SOPs and other GMP documents for QC Manager approval.
- To maintain the equipment according to the SOP and to ensure that the workplace is clean and safe.
- Report to the QC Manager and perform duties as assigned
Requirements
- Diploma or above in Chinese Medicines, Biology, Chemistry, Biochemistry, Microbiology, Pharmaceutical Studies or other related Science subjects.
- At least 5 years of work experience in quality control, preferably in the pharmaceutical industry.
- With solid knowledge of laboratory equipment such as GC, HPLC, TLC, etc.
- Proven ability to write SOPs and GMP documentation independently.
- With experience in equipment validation is an advantage.
- Familiar with MS office.
- Self-motivated and willing to learn.
- Good command in Cantonese and English.
Benefits
We offer 5-day work week, free lunch, shuttle bus, double pay, discretionary bonus and comprehensive benefits to the right candidate.
- 五天工作 5-Day Work
- 年終雙糧 Double Pay
行業 Industry
- 製造 / 工業 Manufacturing / Industrial
工作種類 Job Category
- 物流 / 運輸 / 船務 (船務) Logistics / Transportation / Shipping (Shipping)
- 製造 (品質控制 / 保證及測試 / ISO) Manufacturing (Quality Assurance, Control & Testing / ISO)
工作地點 Location
學歷要求 Education