Responsibilities:
– Maintain relevant documentation to ensure in compliance with PIC/s requirements
– Prepare specifications, SOPs and other GMP controlled documents.
– Maintain and improve product quality, communicate and coordinate with internal parties on quality control issues.
– Support and facilitate audits and regulatory inspection.
– Prepare regular reports and participate in ad hoc projects and other assigned duties.
Requirements:
– High diploma, Degree or above in Pharmacy or Pharmaceutical Science or related science disciplines.
– Preferable with good knowledge of PIC/s
– Familiar with Microsoft Office applications
– Independent, enthusiastic with good communication skills and ability to interact with employees at all levels.
– Good command of spoken and written English and Chinese
– Minimum 1 year working experience in quality assurance of pharmaceutical or related industries
If interested, please send your resume to email: wtyhrd@gmail.com
