Key Roles and Responsibilities

• Assist in planning and executing qualification and validation activities
• Assists in validation documentation preparation, including protocol and report
• Update and maintain validation plan and validation master list
• Prepare qualification and validation related document for quality management systems, i.e. Change control, risk assessment
• Assist in ad-hoc projects assigned by Supervisor

Qualification and Experience 

• Higher Diploma, Associate Degree or Degree holder in Engineering, Pharmaceutical or Science related discipline
• Preferably 0-2 years of working experience in validation
• Fresh graduates will also be considered
• 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 statong 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.