- Actalent (Des Moines, IA)
- …trials. + Review, update and draft new Standard Operating Procedures (SOPs) within the Regulatory Affairs Department as needed. + Review and prepare outlines of ... Oversee regulatory support and compliance in accordance with guidelines...in accordance with guidelines from USDA, FDA, and international regulatory agencies. Responsibilities will be related to new product… more
- Actalent (Des Moines, IA)
- …trials. * Review, update and draft new Standard Operating Procedures (SOPs) within the Regulatory Affairs Department as needed. * Review and prepare outlines of ... statistical analysis, document control, clinical trials, USDA and FDA regulatory support, technical writing, and research and development is advantageous.… more
- Sumitomo Pharma (Des Moines, IA)
- …changes to contract manufacturing organizations, testing laboratories, clinical sites and regulatory affairs as needed. + Responsible for compliance with ... ** Associate Director, GMP Quality Control** Sumitomo Pharma America...ensures compliance with GMPs, SMPA procedures and applicable global Regulatory guidelines by providing oversight and management of the… more
- Sanofi Group (Des Moines, IA)
- …report into the US Medical Immunology team which is a segment of the Medical Affairs Specialty Care organization. Our Medical Affairs function serves as a valued ... strategic partner with Clinical, Commercial, Regulatory , and Market Access on therapeutic solutions to support...Plans. + In coordination with the Field Medical Training Associate Director, ensure MSLs have robust scientific knowledge and… more
- Humana (Des Moines, IA)
- …is committed to advancing the employment experience and vitality of the associate community. Through offerings anchored in a whole-person view of human well-being, ... join the Healthcare Quality Reporting and Improvement (HQRI) organization as Senior Vice President (SVP), Risk Adjustment Operations and Interoperability. This key… more