Quality Control Operations Scientist

Job Responsibilities: · System Configuration: Develop and maintain LIMS/LES applications (e.g., LabWare, Biovia) to support laboratory workflows. ·Workflow Optimization: Collaborate with laboratory personnel to analyze, map, and improve business processes, translating them into digital solutions. · Validation & Compliance: Perform system validation, execute test scripts, and maintain documentation to ensure regulatory compliance. ·User Support & Training: Provide technical support, troubleshooting, and training for laboratory staff, DS and DP on system usage. ·Instrumentation Interfacing: Configure LIMS and instrument middleware to automate data transfer. ·Management of test samples in LIMS/LES: In-process and release samples, environmental testing samples and drug substance and excipient samples ·Configure Stability sample in LIMS. ·Configure Regulatory retain sample in LIMS ·Configure Reference sample in LIMS ·Responsible for all other electronic system application, including but not limit to LIMS, EMPOWER and LES. ·Ensure all the activities in QC team performed with compliance of cGMP, data integrity and EHS requirement. ·To carry out any other tasks assigned by the reporting manager Job Requirements: ·Bachelor degree or above in pharmacy, chemistry, biochemistry, analytical chemistry or other related discipline ·With NLT 2 years in biotech or biopharma ·Deep understanding of FDA, EMA, ICH related regulations ·A good understanding of the overall view of drug development process. ·A thorough understanding of the principles and management of cGMP compliance, and strong quality minds. ·Comprehensive knowledge in FDA, EMA,NMPA, ICH, WHO technical guideline and USP, Eur.P, ChP pharmacopoeias. · Comprehensive knowledge in IND/IMPD,NDA and ANDA filing Contract Duration: 12 months, subject to renewal, based on performance