US_Manufacturing Specialist_CO

Job Title 2-5 years of experience working in manufacturing. Hands-on cGMP manufacture including both upstream virus production and downstream purification. Prepare manufacturing support materials such as media and buffers. Prepare manufacturing equipment such as packing of chromatography columns for the manufacture of clinical and commercial vectors. Participate in investigations of process deviations by conducting data gathering, trending and data presentation as required. Review manufacturing documents and procedures (such as SOPs and batch records) for virus production and purification. Perform routine calculations and maintain appropriate records. Maintain manufacturing equipment and records. Maintain safety procedures and compliance records. Contribute to the manufacturing process monitoring for products transfer from research to manufacturing, as needed.