Roles & Responsibilities
Job Summary
- Perform sample management, including but not limited to :
○ Managing in-process and release samples for product, environmental, and raw material management.
○ Stability sample management.
○ Regulatory retaining of sample management.
○ Reference sample management.
Assist in QC instrument and equipment management, such as C-type instruments including HPLC, GC, IC, and LC-MS, as well as B-type instruments like pH meters, balances, and color meters.Assist in electronic system applications, including but not limited to LIMS, EMPOWER, and LES.Ensuring all activities within the QC team are performed in compliance with cGMP, data integrity, and EHS requirements.Qualifications
Bachelor’s degree or higher in pharmacy, chemistry, biochemistry, analytical chemistry, or other related disciplines,Understanding of the overall drug development process preferredThorough knowledge of cGMP compliance principles and management, with a strong quality mindset.Proficiency in English as a working language.Tell employers what skills you have
Biochemistry
Analytical Chemistry
Drug Development
HPLC
Chemistry
Compliance
LIMS
Sample Management
IC
EHS