Key responsibilities
- Perform sampling and physical, chemical and performance testing of raw materials, in-process materials and finished products using approved methods and specifications.
- Execute complex, critical, non-routine or high-priority tests independently within established methods and authorization limits.
- Support QC Operators with routine digital workflows and basic ERP (Enterprise Resource Planning, i.e. SAP) system data entry, performing first-level checks on digital records and escalating IT or system issues when needed.
- Review laboratory worksheets, calculations and test records prepared by QC Operators for completeness, traceability and obvious inconsistencies before escalation to the QC Manager.
- Support allocation of daily laboratory work, prioritization of urgent samples and communication of status to the QC Manager.
- Perform first-level troubleshooting for test execution, sample preparation, equipment operation and data-recording issues; document actions and escalate unresolved matters.
- Identify, contain and promptly escalate atypical results, OOS (Out-of-Specification) / OOT (Out-of-Trend) indications, method deviations, sample issues, equipment failures and potential data-integrity concerns.
- Provide structured on-the-job training and practical qualification support for QC Operators on approved methods, sampling, equipment use, documentation and laboratory discipline.
- Support verification of equipment readiness, calibration status, sample archives, reagent/consumable availability and housekeeping.
- Participate in pre-production checks, routine process/product verification and investigations assigned by the QC Manager.
- Contribute technical observations to trend analysis, method optimization, SOP(Standard Operating Procedure) updates and continuous-improvement initiatives.
Decision authority
- Prioritizes assigned work and provides operational direction to QC Operators during the shift or day, in line with the QC Manager’s plan.
- Verifies technical completeness of routine records before managerial approval.
- May stop or suspend an analysis when safety, equipment status, sample identity or data integrity is in doubt; must document and escalate immediately.
- In the absence of QC Manager can authorize final result approval, product release, lot disposition, deviation closure, CAPA (Corrective and Preventive Action) closure or specification changes.
Key interfaces
- QC Manager, QC Operators, Production supervisors, R&D technical staff, Maintenance for routine operational coordination and IT support / ERP key users for routine issue escalation.
Success measures
- Quality and timeliness of assigned testing and technical record review.
- Percentage of junior team members trained and qualified as planned.
- First-level troubleshooting effectiveness and repeat-error reduction.
- Compliance of assigned equipment, records, samples and work areas.
