Key Roles and Responsibilities

• Reviews manufacturing process batch record and monitors sterile eye-drop manufacturing line
• Conducts self-inspection and environmental control in facility, i.e. oral solid and liquid unit, sterile unit, packaging unit and warehouses
• Assists to supervise routine manufacturing, line clearance, raw material receiving and disposal
• Assists to prepare SOP policies on quality operations, i.e. environmental monitoring, product release
• Assists in ad hoc projects as assigned by Supervisor

Qualification and Experience

• Bachelor degree in science, pharmaceutical or engineering related discipline
• Fresh graduates are considered; preferably with quality operation management knowledge and experience
• Experience in pharmaceutical industry is an definite advantage
• With good communication skill, hard-working, willing to learn
• Proficiency in PC applications, including MS Office
• Good communication skills in both written and spoken English and Cantonese 

How to Apply 

You are invited to send in your application and CV stating the position (with reference number) you are applying for together with your current and expected salary, either by email or mail HR Dept, 1/F., GMP Centre, Tai Po Industrial Estate, Tai Po, N. T., Hong Kong.

Jean-Marie Pharmacal Co. Ltd. is an Equal Opportunities Employer. Personal data provided by job applicants will be used strictly in accordance with our personal data policy and for recruitment purposes only. We aim to respond to successful applicants within 8 weeks and related information will be kept in our file for up to 12 months for other suitable vacancies in our organization and thereafter destroyed.