Job Description: The Deviation Management Contractor will be responsible for deviation management activities in support of vaccine production at the West Point site. This engineer will be a member of the Technical Operations Deviation Management team within the ROTA End-to-End (E2E) technical operations unit. The primary responsibility of the individual will be investigation initiation and closure associated with vaccine technology/production in support of the operations taking place in the ROTA E2E. Support will be focused on the Deviation Management process including operations support, equipment troubleshooting, implementation of process/equipment actions, and other related duties. This position will require development of technical expertise of process and product knowledge. This is position is a site-based assignment and requires the employee to work at the site M-F. Two days of remote work per week may be available, work permitting, but is not guaranteed. Off-shift or weekend coverage may be required based on business unit needs and specific assignments. Responsibilities include: • Leads and/or works as a team member on manufacturing investigations and/or process improvement projects. • Has ability to examine an issue from diverse perspectives (safety, compliance, automation, equipment, process, and people) in order to identify root cause and propose effective corrective and preventative actions (CAPAs). • Assures consistent application of standardized work, engineering, and process tools. • Provides technical support to manufacturing shop floor for problems and issues. • Conducts and designs experimental protocols as needed using the Technical Operations lab facilities and/or production equipment at full scale. • Writes technical documents to support closure of deviations using the SAP system. • Authors and updates technical and manufacturing documents necessary for investigations, process design/definition, engineering studies, process demonstrations, change control and validation.

Responsibilities: The Deviation Management Contractor will be responsible for deviation management activities in support of vaccine production at the West Point site. This engineer will be a member of the Technical Operations Deviation Management team within the ROTA End-to-End (E2E) technical operations unit. The primary responsibility of the individual will be investigation initiation and closure associated with vaccine technology/production in support of the operations taking place in the ROTA E2E. Support will be focused on the Deviation Management process including operations support, equipment troubleshooting, implementation of process/equipment actions, and other related duties. This position will require development of technical expertise of process and product knowledge. This is position is a site-based assignment and requires the employee to work at the site M-F. Two days of remote work per week may be available, work permitting, but is not guaranteed. Off-shift or weekend coverage may be required based on business unit needs and specific assignments. Responsibilities include: • Leads and/or works as a team member on manufacturing investigations and/or process improvement projects. • Has ability to examine an issue from diverse perspectives (safety, compliance, automation, equipment, process, and people) in order to identify root cause and propose effective corrective and preventative actions (CAPAs). • Assures consistent application of standardized work, engineering, and process tools. • Provides technical support to manufacturing shop floor for problems and issues. • Conducts and designs experimental protocols as needed using the Technical Operations lab facilities and/or production equipment at full scale. • Writes technical documents to support closure of deviations using the SAP system. • Authors and updates technical and manufacturing documents necessary for investigations, process design/definition, engineering studies, process demonstrations, change control and validation.

Qualifications: Education Minimum Requirements: • B.S. degree in Engineering or Sciences. Required Experience and Skills: • Minimum one (1) year post-bachelor's degree experience in a GMP (good manufacturing practices) manufacturing and/or technical support of GMP manufacturing operations (or M.S. degree with < 1 year experience). • Demonstrated ability to drive results to hit assigned due dates. • Strong communication, collaboration skills and ability to drive accountability. • Strong problem-solving skillset Preferred Experience and Skills: • Vaccine manufacturing • Sterile processing • Experience authoring