- job summary: Responsibilities: Manage various digital projects/ initiatives for the Digital Operations team. This includes: schedule and lead meetings, create status reports, update and maintain Project Plans, and represent the team on meetings. Manage Medicare and Medicaid Regulatory submissions of Website and Portal content. location: Saint Louis, Missouri job type: Contract salary: $51 - 61 per hour work hours: 8am tojob summary: Responsibilities: Manage various digital projects/ initiatives for the Digital Operations team. This includes: schedule and lead meetings, create status reports, update and maintain Project Plans, and represent the team on meetings. Manage Medicare and Medicaid Regulatory submissions of Website and Portal content. location: Saint Louis, Missouri job type: Contract salary: $51 - 61 per hour work hours: 8am to
- job summary: Typical Day in the Role: Daily or weekly stand up interaction with the teams based on the project deliverables. Typical tasks will shift based on deliverables. This resource will be responsible for building data pipelines and modeling within Snowflake using Talend and other data integration tools.Daily schedule will follow regular business hours, no overtime needed.Resource will interact with Hiring Manager and other devs/tech leads.job summary: Typical Day in the Role: Daily or weekly stand up interaction with the teams based on the project deliverables. Typical tasks will shift based on deliverables. This resource will be responsible for building data pipelines and modeling within Snowflake using Talend and other data integration tools.Daily schedule will follow regular business hours, no overtime needed.Resource will interact with Hiring Manager and other devs/tech leads.
- job summary: Your Role: With minimal supervision, the Regulatory Affairs Expert-Medical Devices manages assigned regulatory tasks related to health authority notifications, submissions, and registrations regarding renewals and new products, and changes to products or sale of products ensuring continual compliance to all applicable regulations and ensuring that site regulatory strategy aligns with overall corporate regulatory strategy, goals, and objectijob summary: Your Role: With minimal supervision, the Regulatory Affairs Expert-Medical Devices manages assigned regulatory tasks related to health authority notifications, submissions, and registrations regarding renewals and new products, and changes to products or sale of products ensuring continual compliance to all applicable regulations and ensuring that site regulatory strategy aligns with overall corporate regulatory strategy, goals, and objecti
- job summary: A Process Engineer is needed for a global healthcare leader that discovers, develops and distributes therapeutic solutions focused on patient's needs in the St. Louis, MO area. The role involves providing technical support, process monitoring, and data analysis for commercial mammalian cell culture processes at external manufacturing sites, with responsibilities including troubleshooting, deviation resolution, and collaboration with cross-funjob summary: A Process Engineer is needed for a global healthcare leader that discovers, develops and distributes therapeutic solutions focused on patient's needs in the St. Louis, MO area. The role involves providing technical support, process monitoring, and data analysis for commercial mammalian cell culture processes at external manufacturing sites, with responsibilities including troubleshooting, deviation resolution, and collaboration with cross-fun
