Key Roles and Responsibilities

• Perform sampling and inspection of the received incoming materials (chemical and packaging material).
• Perform and monitor the calibration and maintenance of equipment.
• Assist to maintain the documentation system in compliance with GMP and/or ISO requirement.
• Prepare the document relating quality control procedures, standards, and specifications.
• Perform sampling and testing of in-process product and FP.
• Participate audit.
• Participate Ad hoc project assigned.
• Assist in OOS and divergence investigations and follow up if necessary.

Qualifications and Experience

• Higher Diploma or above in Chemistry, Pharmaceutical or related discipline.
• Knowledge of GMP and/or ISO standards.
• At least 2 years relevant experience in commercial testing laboratory or pharmaceutical laboratory.
• Extensive knowledge and experience in UV-Vis and other analytical instrument e.g. HPLC.
• Good PC Skill, analytical skills and communication skill.
• Hardworking, organized, initiative, self-motivated.

How to Apply

You are invited to send in your application and CV stating the position with reference number JGM2002-004 or mail Room 2313-18, Tower 1, Millennium City 1, 388 Kwun Tong Road, Kwun Tong, Kowloon on or before 19 April 2020.

Jacobson Group Management Limited 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.