Responsibilities:

• Supervise day-to-day running of QC Chem. laboratory
• Monitor routine testing Turnaround Time
• Supervise and train QC staff
• Perform test method development and validation
• Prepare and revise SOP and other relevant quality control documents
  

Requirements:

• Higher Diploma or Degree holder in Chemistry, Analytical Chemistry, Biology, Pharmaceutical Studies or related discipline
• Familiar with analytical instruments such as HPLC, UPLC, GC, ICP and IR
• 3 years working experience or above in pharmaceutical company or commercial testing laboratory and 2 year experience at supervisory level
• Initiative, organized, hard working, strong leadership and problem solving skills
• Less experience will be considered as Assistant QC Supervisor 

We offer an attractive compensation package and a comprehensive 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:-