Purpose of Role To ensure the accuracy consistency and reliability of all raw materials in-process samples and finished enzyme products through structured testing documentation and compliance The QC Executive is responsible for maintaining product quality standards supporting production through timely analysis ensuring adherence to SOPs and strengthening laboratory discipline The role requires ownership precision and technical accountability to maintain the company s reputation for quality excellence Key Results Expected 1 Testing Accuracy Timely Reporting - 100 completion of all assigned sample testing within daily and batch timelines - Zero delays in reporting results to Production and QA 2 Compliance Process Discipline - Adherence to all SOPs testing protocols and safety norms - Accurate and complete documentation in all logs registers and formats 3 Quality Assurance Support - Reduce testing errors deviations and non-conformities - Strengthen alignment between QC Production and R D 4 Lab Management Equipment Handling - Ensure proper calibration cleanliness and maintenance of instruments - Control inventory of chemicals reagents glassware and consumables 5 Risk Issue Identification - Highlight testing deviations unusual results and quality risks immediately - Minimise rework retesting and batch rejection through accuracy and foresight Core Responsibilities Actionable 1 Laboratory Testing Analysis - Collect and test raw material in-process and finished product samples as per SOPs - Conduct physicochemical tests pH viscosity moisture enzyme activity stability etc - Support microbial limit testing where required - Ensure correct sample labelling traceability and timely analysis - Cross-check test results before entry to avoid inaccuracies 2 Equipment Handling Calibration - Operate instruments such as pH meter viscometer UV spectrophotometer moisture analyser incubator etc - Perform routine calibration and maintain calibration records - Report equipment malfunction immediately to seniors 3 Documentation Reporting - Maintain all logs sample registers calibration logs test sheets batch reports COAs - Ensure 100 accuracy of data entry in digital and physical formats - Maintain revision logs and lab records in compliance with GLP GMP - Submit structured daily weekly QC reports 4 QA Production R D Coordination - Share test results promptly with Production for batch continuation or correction - Support QA in deviations CAPA and audit preparation - Assist R D in experimental testing and trial batches - Escalate out-of-spec OOS findings systematically 5 Lab Safety Housekeeping - Follow all PPE chemical handling and safety norms - Maintain a clean organised and audit-ready laboratory - Dispose of waste as per safety SOPs 6 Process SOP Adherence - Follow checklists testing protocols formatting standards and sample flows - Ensure testing and documentation comply with ISO FSSAI if applicable and internal QC standards - Support improvement of SOPs and testing methods Job Types Full-time Permanent Pay 15 000 00 per month Perks Commuter assistance Provident Fund Work Location In person

📌 Qc Chemist (Gujarat)
🏢 TalentGuru
📍 Gujarat