job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treat
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treat
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-fun
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-fun
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 objecti
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 objecti
job summary: Typical Day in the Role Schedule: standard, 8-5PM CSTInteraction: Will work collaboratively and independently to complete task. Video meetings are a must to ensure productive engagement. Candidate will interface with Business Users and technical teams throughout day to day.Environment: highly collaborative and fast paced environment. Candidate must be a very seasoned IAM technical analyst that can jump in with limited direction and follow
job summary: Typical Day in the Role Schedule: standard, 8-5PM CSTInteraction: Will work collaboratively and independently to complete task. Video meetings are a must to ensure productive engagement. Candidate will interface with Business Users and technical teams throughout day to day.Environment: highly collaborative and fast paced environment. Candidate must be a very seasoned IAM technical analyst that can jump in with limited direction and follow
job summary: Job Profile Summary Position Purpose: Designs, develops, and implements complex enterprise software solutions.Collaborates closely with technical and non-technical roles such as data modelers, architects, business analysts, data stewards, and subject matter experts (SMEs) to provide design, technical analysis, development/configuration, testing, implementation, and support expertise representing the interest of the business across the enter
job summary: Job Profile Summary Position Purpose: Designs, develops, and implements complex enterprise software solutions.Collaborates closely with technical and non-technical roles such as data modelers, architects, business analysts, data stewards, and subject matter experts (SMEs) to provide design, technical analysis, development/configuration, testing, implementation, and support expertise representing the interest of the business across the enter
job summary: - This role is part of the Bioprocess Research & Development Cell Banking team responsible for the manufacturing and testing of GMP cell banks used to produce clinical and commercial biopharmaceutical product location: Chesterfield, Missouri job type: Contract salary: $23.26 - 27.00 per hour work hours: 9 to 5 education: High School responsibilities: Conduct cell bank manufacturing operations as required. Follow and adhere
job summary: - This role is part of the Bioprocess Research & Development Cell Banking team responsible for the manufacturing and testing of GMP cell banks used to produce clinical and commercial biopharmaceutical product location: Chesterfield, Missouri job type: Contract salary: $23.26 - 27.00 per hour work hours: 9 to 5 education: High School responsibilities: Conduct cell bank manufacturing operations as required. Follow and adhere
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