At AliveDx, we empower diagnostic insights, transform patient care, and innovate for life. With over 30-years in in-vitro diagnostics, we put the health of patients first by creating innovative solutions designed for faster diagnostic results. Alba–– our blood bank reagents portfolio–– and MosaiQ®–– one of the first multiplexing and multimodality automated testing platforms––are designed to make labs more efficient and clinical decision-making more effective. Our journey started as Alba Bioscience, and later, Quotient. Today, as AliveDx, we innovate for life.

• Conduct all duties in compliance with Good Manufacturing Practice (GMP), Good Documentation Practice (GDP) and appropriate regulatory requirements.
• Execute and control specific processes and test procedures in accordance with SOP’s, GMP and Health and Safety Policies ensuring consistency and compliance with all operational policies.
• Analyse and record data in batch manufacturing records and other relevant documentation to provide a permanent and precise record of all work carried out to ensure regulatory compliance.
• Participate in the routine Quality Control testing of intermediate and final product manufactured at Quotient (Serological, depending on area).
• Preparation of reports as required.
• Assist with the training of staff in order to ensure continuous development of staff capabilities.
• Monitor the safe operation control and maintenance of equipment in accordance with established procedures to minimise delays to work programmes and ensure a safe working environment.
• Participate in projects as required to ensure continuous improvement/development of products and processes