Key Roles and Responsibilities

• Assist the Production Manager in developing, implementing and maintaining the documentation system, including the Standard Operating Procedures (SOPs) & Batch Production Records
• Ensure and 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
• Ensure qualification & validation activities are performed as per prescribed schedules
• Monitor performance of plant workers and ensure GMP requirements of all on-going activities is fully complied.
• Mainly focus on Solid or Liquid production line
• To perform the daily operation and ad-hoc functions of Production Department

Qualification and Experience

• Relevant experience in GMP pharmaceutical manufacturing is preferred
• 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
• Less experience will be considered as Assistant Production Officer
• Fresh graduate are welcome

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.