- US Tech Solutions (North Chicago, IL)
- …management **Preferred Experience:** 1-2 years pharmaceutical experience including 1-2 years in regulatory affairs , R&D, or **Manufacturing (CTD Module 3)** + ... coordinate activities with all functional departments in support of regulatory filings. + Manage, compile, and **author CMC...and accomplish goals. Performs a variety of tasks. May lead and direct the work of others. A wide… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …activities. Team Leadership * Lead , mentor, and retain a high-performing Regulatory Affairs team, including Regulatory Operations, Labeling, and ... **Overview** The Vice President of Regulatory Affairs will serve as the...across components. Marketed Product Compliance & Lifecycle Management * Lead regulatory oversight for marketed products, including… more
- Lundbeck (Deerfield, IL)
- …in the greater United States** **SUMMARY:** The Director, US Regulatory Affairs Global Strategic Labelling will lead and oversee the development of ... products/programs. + Trains, develops, and manages an effective regulatory affairs cross-functional team on key labelling requirements ( CMC , Regulatory… more
- Lundbeck (Deerfield, IL)
- …development programs. + Trains, develops, and manages an effective regulatory affairs cross-functional team on a dotted-line basis ( CMC , Regulatory ... Opportunity - Open to candidates within the United States** The Director, US Regulatory Affairs Strategy, oversees the implementation of regulatory … more
- AbbVie (North Chicago, IL)
- …such as analytical, process engineering, internal and external manufacturing, quality assurance, CMC regulatory affairs , supply chain and Operations ... Care group is seeking a motivated Scientist as a CMC drug product project lead , specifically for...+ Ability to influence internal and external experts on CMC regulatory issues, independently. + Demonstrated excellence… more