Key Duties and Responsibilities
Conduct laboratory-based analysis of quality control (QC) samples to support validation of biological and diagnostic products. Assist in the evaluation and interpretation of QC data, identifying trends, anomalies, and deviations in experimental results. Perform systematic data entry, management, and analysis using laboratory information management systems (LIMS) and QC databases. Participate in the investigation of non-conformances, including root cause analysis and implementation of corrective and preventive actions (CAPA). Support the inspection and scientific review of production records, ensuring compliance with quality standards and regulatory requirements prior to product release. Contribute to the development, review, and maintenance of scientific and technical documentation, including standard operating procedures (SOPs) and validation protocols. Operate, calibrate, and maintain laboratory instruments and automated production systems (e.g., diagnostic platforms and robotics) to ensure accuracy and reliability of results. Apply laboratory best practices, including contamination control, equipment sterilisation, and adherence to biosafety and quality assurance protocols. Monitor laboratory inventory, including biological reagents and consumables, ensuring availability and proper storage conditions. Assist in the preparation, packaging, and labelling of biological products in accordance with scientific and regulatory specifications. Collaborate with cross-functional teams, including warehouse and distribution units, to coordinate product release timelines based on QC outcomes. Maintain accurate experimental records and documentation to support traceability, audits, and continuous improvement initiatives. Pay: From $76,000.00 per year Work Location: In person
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