Key Roles and Responsibilities
- Assist in implementing and maintaining the documentation system and quality management system
- Responsible for document (SOP, Specification, etc) preparation and review
- Arranging repacking of pharmaceutical products
- Assist in performing ad hoc projects and other QA-related duties such as risk assessment, change control, internal audit……
Qualifications and Experience
Diploma level or above in Sciences studiesFamiliar with ISO9001 / ISO 13485 / Medical devices / GDP environment is an advantageOver or at 3 years of relevant working experience will be considered as Quality Assurance OfficerProficient in MS Office application (Excel, Word & PowerPoint) and Chinese Word ProcessingHardworking, initiative, self-motivated, team player and fast learnerFresh graduates are also consideredImmediate available is highly preferred