Key Roles and Responsibilities

• Define and plan validation activities to meet the cGMP requirements
• Coordinate with end users and process owners to develop and execute validation protocols for manufacturing facilities, systems, process and / or software
• Ensure validation activities are completed timely. Analyze validation related issues, implement validation related event, Change Control and CAPA
• Analyze validation results statistically and write reports summarizing results
• Participate in new project initiation, planning, execution and controlling
• Perform other related duties within scope of the department.

 Qualification and Experience 

• Higher Diploma, Associate Degree or Degree holder in Science, Pharmaceutical, Engineering,  or related discipline
• Good interpersonal and teamwork skills, hard-working, willing to learn
• Good language skills in both written and spoken English and Cantonese 
• Candidates with less experience will be considered as Assistant Q.A. Validation Officer/Engineer
• Relevant work experience is preferred but not essential
• Fresh graduates are welcome

 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

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.

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:-