Responsibilities:

• Implement corporate policies and maintain GMP documentation system in a GMP pharmaceutical plant
• Perform routine inspection on products at various stages on the production line to implement the GMP policy
• Assist in performing ad hoc project and other QA-related duties
• Responsible for handling internal audit, product registration and product complaints

Requirements:

• Higher Diploma or Degree holder in Pharmaceutical Studies or other science related discipline
• Hands-on GMP experience in pharmaceutical industry will be an definite advantage
• Hardworking, initiative, self-motivated and fast learner
• Good knowledge of MS office, PowerPoint, Excel and Chinese word processing
• Suitable candidate with less experience/qualification may be considered as Assistant QA Officer

We offer attractive compensation package and training program. Please send your resume with current and expected salary to: HR Dept, 1/F., GMP Centre, Tai Po Industrial Estate, Tai Po, N. T., Hong Kong or e-mail to hr@jmp.com.hk.

All personal data collected will be used for recruitment related purpose only.

We are a leading GMP pharmaceutical manufacturer with a firmly established local and international presence, operating through a strategically and carefully expanded network in both local and overseas pharmaceutical industry. With over 50 years of experience in the health-care industry, Jean-Marie is strongly committed in manufacturing and developing excellent quality pharmaceutical products. To facilitate our strategic planning in further developing our pharmaceutical business, we now invite suitable candidates to fill the following position:-