Prepare and revise QC SOP and GMP documents, assist in implementing and maintaining the documentation system, prepare validation and qualification documents, conduct product quality review, develop QC training program.
Key Roles and Responsibilities
- Prepare and revise QC SOP and GMP documents
- Assist in implementing and maintaining the documentation system
- Assist in preparing the validation and qualification documents
- Responsible for QC training program
- Responsible for Product Quality Review
- Responsible for Report / Logbook checking
- Prepare QC purchase order and inventory control record
- Provide clerical and administrative support
- To perform any duties as assigned
Qualification and Experience
- Higher Diploma, Associate Degree or Degree holder in Biology, Chemistry, General Science or related discipline
- Good team player, self-motivated and fast learner
- Good attitude, hardworking and able to work under pressure
- Good PC Skills including MS Words, Excel and Chinese word-processing
- Less experience will be considered as Assistant QC Officer
- Fresh graduate will also be considered