Key duties and responsibilities include:

• 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