Responsibilities:
Prepare and revise QC SOP and GMP/PICs documents
Implementing and maintaining the documentation system
Responsible for QC training program
Responsible for Product Quality Review
Prepare QC Purchase Order and Inventory Control
Provide clerical and administrative support
To perform any duties as assigned
Requirements:
Higher Diploma holder or above in Chemistry / Biology / Pharmaceutical or related discipline
2-3 years' relevant experience in commercial testing lab or pharmaceutical lab is advantageous
Knowledge of GMP and/or ISO standards
Hardworking, initiative, self-motivated
Able to work under pressure, and willing to work overtime
Hands-on experience in ICP, GC, HPLC and other analytical instrument is advantageous (for chemistry laboratory staffs)
Team player with good interpersonal & communication skills
Fresh graduates are welcome
We offer attractive remuneration package including medical scheme, discretionary year-end bonus. Interested parties please send full resume, starting date of available and salary expectation via email for interview. We regret that only shortlisted candidates will be informed.
Synco (H.K.) 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.
- Personal data collected will be used for recruitment purpose only *