Quality Control Analyst

Key ResponsibilitiesManage the storage and inventory of laboratory samplesConduct analytical testing and documentation for APIs, drug substances/products, complaints, packaging materials, and stability samplesEnsure strict compliance with cGxP standards, including data integrity requirementsExecute and document stability testing (if not centralized), including storage, testing, and reporting to cGxP standardsFollow all Health, Safety, and Environment (HSE) guidelinesIdentify and report safety risks or potential incidents, and propose preventive solutionsParticipate in mandatory training and retraining programsSupport operations during rotating day/night shiftsRole RequirementsEssential Qualifications and ExperiencePrior experience in a laboratory setting within the pharmaceutical industry (QA, production), with exposure to aseptic techniques preferredProficiency in administrative and documentation tasks compliant with GMP and HSE standardsDemonstrated strengths in:

Breakthrough analysis and problem-solvingResilience and adaptabilityOperational efficiency and continuous learningDigital fluency and technical skillsTechnical CompetenciesHands-on knowledge of laboratory instruments and QC testing proceduresStrong command of GxP, TQM principles, and lab excellence standardsAbility to maintain QC IPC/DS laboratory equipment and systems in accordance with cGMP complianceCompetent in executing product testing within timelines and contributing to validation and method transfer protocolsSkilled in performing routine in-process, release, and stability testing, including documentation reviewCapable of supporting lab investigations and leading root cause analysisDetail-oriented in preparing and verifying QC documentation to ensure accuracy, consistency, and regulatory complianceProactively identifies opportunities to optimize testing proceduresSupports audit readiness and participates in internal audits and inspections by health authorities