- 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: - 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 adherejob 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
