Responsibilities:

• Assist the Production Officer / Manager in developing, implementing and maintaining the documentation system, including the Standard Operating Procedures (SOPs) & Batch Production Records.
• Maintain adequate and accurate records for controlling and monitoring conformity to specified GMP and statutory requirements.
• Assist in monitoring the calibration & maintenance program of production equipment and facility.
• Assist the qualification & validation activities as per prescribed schedules.
• To perform the daily operation and ad-hoc functions of Production Department.

 Requirement:

• IVE graduate or above in Pharmaceutical Technology/Pharmacy, Chemistry/Chemical Engineering or other Science related disciplines. Fresh graduates will also be considered;
• Relevant experience in GMP pharmaceutical manufacturing is preferred but NOT a must;
• Familiar with MS office and Chinese word processing;
• Hardworking, initiative, self-motivated and fast learner;
• Able to work under pressure and willing to work overtime;
• Good interpersonal skill and communication skill.

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:-