MedImmune is the worldwide biologics research and development arm of AstraZeneca, a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of small molecule and biologic prescription medicines. MedImmune is pioneering innovative research and exploring novel pathways across key therapeutic areas, including respiratory, inflammation and autoimmunity; cardiovascular and metabolic disease; oncology; neuroscience; and infection and vaccines. RESPONSIBILITY: The QC intern will perform laboratory information management system database entry, routine laboratory duties, and documenting results according to SOPs and cGMPs. The QC intern will perform assigned duties according to established SOPs and cGMPs. The QC intern will file and archive QC records. The QC intern will be responsible to perform assigned duties as scheduled and to work independently. PRINCIPLE DUTIES: Perform scheduled and unscheduled assignments according to SOPs and cGMPs Document results according to SOPs and GMPs. Review data for compliance to specifications and reports abnormalities. Perform data entry. Maintain laboratory areas and instrumentation according to maintenance schedules, SOPs and GMP requirements. Normally receives detailed instructions for all assignments. Accurately perform testing, maintain documentation and prepare reports in association with the performing of tests. Read, understand and follow SOPs and comply with current Good Manufacturing Practices as required by the FDA. Read, understand and follow SOPs to comply with GLP/GMP regulations. Maintain documentation to conform to GMPs. Maintain supply levels for performance of assigned duties. Maintain accurate and updated laboratory notebooks and records. Participate in GMP audits. Follow all safety regulations as indicated in the MedImmune Policies and Procedures and accepted lab practice (e.g. wearing of personal protective equipment such as eye protection and lab coats) |
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