Responsibilities

Report to Supervisor-QA (Repackaging) / QAO of licensed GMP repackaging site, handle QA works of our pharmaceutical GMP repackaging site in Shatin Areas, including:

• Handle Daily repackaging operation like checking of material release document and batch repackaging record (BPR) before approval by QAO
• Assist QAO in preparation and facilitate proper implementation of QA SOP
• Support selected principal’s printed packaging material management project, like liaison with principal’s regulatory affairs team for preparation of printing artwork, checking printing company’s printing prototype, etc.
• Handle ad-hoc QA work of company QA team

Requirements

• University graduate of Science Subject, or
• Higher Diploma / Diploma holder of subject of Pharmaceutical / Food Science / Quality Management      
• One year or more working experience in Pharmaceutical industry, especially in GMP manufacturer, is highly preferred
• Proficiency in both written and spoken English and Chinese

We offer opportunities for development in addition to a competitive salary and fringe benefits to the right candidates. Please quote the reference number on your application.

All applications received will be used exclusively for recruitment purposes only. Applicants who are not contacted within 8 weeks should consider their application unsuccessful for the position advertised. Data supplied by applicants will be kept for 6 months.

LF Asia, a member of DCH Holdings, is Asia’s fastest-growing distribution service provider specializing in food, healthcare, beauty and cosmetic products in Greater China and Asean countries. As LF Asia expands, we are looking for high caliber individual to fill the following positions.  

We offer opportunities for development in addition to a competitive salary and fringe benefits to the right candidates. Please email your detailed resume with contact telephone numbers, current and expected salary to HKGLFAHR@lfasia.com.