QC Analyst
About this position
Responsibilities
• Perform physical tests of bulk products and finished products following PLM specification and SOP.
• Perform sample preparation for uniformity of content and sample preparation for other testing parameter for support bulk/finished product release to production and market.
• To ensure that product test results are testing, checked, approved, recorded and available for inspection in accordance with Good Manufacturing & Control Laboratory Practices.
• Be responsible for preparation and chemical reagent solution or mobile phase comply with test method. Be responsible for management of chemical reagents and chemical solution have proper storage and inventory control.
• To ensure that equipment, instrument is maintenance, calibrated in QC laboratory Accountable for ensuring laboratory investigations are thorough and accurate and escalation of confirmed Out Of Specification (OOS) and Out Of Trend (OOT) results in line with global standards and any local SOPs.
• To understand and follow all necessary Health & Safety systems and ensure that work is consistent with safe working practices.
• Be responsible for all SOP related to laboratory, product and safety.
• Be responsible for retention of product good sample management system.
• To provide effective application of analytical investigation and change management within QC as defined in SOPS.
• Co-responsible for housekeeping, cleanliness and safety in the laboratory, also responsible for taking care of laboratory facilities to keep them in good condition and ready for use.
• Be responsible for waste management by separate waste following SOP before deliver to contractor.
Requirements
• Bachelor’s degree in science of chemistry, or related filed.
• Experience in analytical instrument such as HPLC, GC, Spectrophotometer, Auto Titrator, Karl Fisher, and water activity are plus.
• Good Command in English, both written and read.
• MS office skills (Excel) at basic level.
• SAP Knowledge/SAP Experience would be advantage.