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| Regulatory And Safety Jobs |
| Clinical Development & Regulatory Affairs Consultant [6026] - Work At Home Responsible for providing consultation/strategic input on regulatory processes for FDA and CPMP submissions. Execute content development of scientific materials required for regulatory submissions and presentations. Day-to-day management and training and development of regulatory and clinical services team members. |
| Clinical Development & Regulatory Affairs Consultant [6025] - Ohio Responsible for providing consultation/strategic input on regulatory processes for FDA and CPMP submissions. Execute content development of scientific materials required for regulatory submissions and presentations. Day-to-day management and training and development of regulatory and clinical services team members. |
| Clinical Development & Regulatory Affairs Consultant [5959] - Work At Home Responsible for providing consultation/strategic input on regulatory processes for FDA and CPMP submissions. Execute content development of scientific materials required for regulatory submissions and presentations. Day-to-day management and training and development of regulatory and clinical services team members. |
| Clinical Development & Regulatory Affairs Consultant [5958] - Ohio Responsible for providing consultation/strategic input on regulatory processes for FDA and CPMP submissions. Execute content development of scientific materials required for regulatory submissions and presentations. Day-to-day management and training and development of regulatory and clinical services team members. |
| Stability Coordinator [5668] - Illinois Coordinate and perform all activities related to the Stability, Annual Product Review and Product Retention Evaluation programs in compliance with Company SOPs and cGMP Regulations. |
| Quality Assurance Inspector [4606] - Illinois Ensure compliance with cGMPs, Company SOPs and FDA regulating requirements during all phases of operations. |
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