工作職責:

• 監測生產流程及產品質量
• 填寫相關記錄及一般文書工作

入職條件:

• 中五程度
• 懂讀寫中文
• 略懂讀寫英文
• 具食品製造業或GMP經驗優先
• 五天工作, 早更 (工作時間: 8:30-13:00)

Job responsibilities:

• Perform routine inspection on various stages of the production line to implement GMP policy
• Assist in maintaining the documentation system
• Assist in other ad-hoc project and other QA-related duties

Requirements:

• F.5 or above
• Attention to details, hard-working and being able to work under pressure;
• Strong communication skill
• Minimum of 2 years relevant experience;
• Experience in pharmaceutical is preferred;
• 5 days work week, morning Shift (Working time: 8:30-13:00)

有意者請將履歷及期望待遇、可到任日期按APPLY NOW申請。

所收集的個人資料只適用於招聘及甄選用途。在使用求職者所提供的個人資料時，僱主會嚴格遵守其個人資料政策的規定。根據<<個人資料(私人)條例>>你有權要求查閱或更改你的個人資料。如你欲行使這項權利，請將你的要求以書面向人力資源部提出。

We offer attractive remuneration package including medical scheme, discretionary year-end bonus etc. Interested parties please send full resume with salary expectation and availability by click "Apply Now". Only shortlisted candidates will be interviewed.

Synco (H.K.) Ltd is an Equal Opportunities Employer. Personal data provided by job applicants will be used strictly in accordance with our personal data policy and for recruitment purposes only. We aim to respond to successful applicants within 8 weeks and related information will be kept in our file for up to 12 months for other suitable vacancies in our organization and thereafter destroyed. 

We are well-established local GMP manufacturer & distributor of prescription and OTC pharmaceuticals, nutritional and health supplements. To support expansion plans, we are looking for a suitable candidate with the required capabilities to fill the following position.