Key Roles and Responsibilities

• Operate all quality related activities in Good Manufacturing Practice ensuring safety and quality of drug manufactured
• Review process control plan, drive quality issues to root cause, corrective and preventive actions, track drug quality performance etc
• Assist drug regulatory registration in Hong Kong and overseas
• Perform ad-hoc tasks as assigned by Supervisor

 Qualification and Experience

• Higher Diploma, Associate Degree or Degree holder in science, pharmacy, pharmaceutical or engineering related discipline
• Fresh graduates are welcomed
• Successful candidate is provided great opportunity to join the challenging and rewarding drug manufacturing industry especially during the COVID pandemic
• Possess good communication skill, willingness to learn, attention to details and hardworking attitude
• No experience required but good communication skill, good command of written and spoken English and Chinese essential

What we offer

• Free shuttle to/from the following locations: Sheung Shui, Tai Wo, Fanling, Tsuen Wan, Tai Po, University Station, Sha Tin, Tuen Mun, Yuen Long, Kowloon Tong, Kwun Tong, Kowloon Bay, Chai Wan, Tai Koo, Tin Shui Wai
• Diversified learning opportunities
• Rapid growth opportunities for strong performers
• Casual attire at work

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.