Responsibilities:

• Assist Production Manager in supervising and scheduling of sterile product (Injectables & Eyedrops) production in a GMP certified Sterile Manufacturing Plant.
• Perform troubleshooting to ensure smooth and efficient daily operations of the plant.
• Monitor performance of plant workers and ensure GMP requirements of all on-going activities is fully complied.
• Ad-hoc duties as assigned by the Management.

 Requirement:

• IVE or above in Chemical/Microbiology/Pharmaceutical Studies, Chemical/Biomedical Engineering or other science related disciplines
• Minimum 1 year solid experience preferably in pharmaceutical GMP certified plant
• Experience in manufacturing of sterile products is an advantage but not a must
• Good communication and interpersonal skills
• Computer knowledge in MS Office and Chinese Word Processing

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:-