Job Opportunity
The Director CMC Regulatory Affairs leads the development of global regulatory strategies for assigned drug/device portfolios.
* Oversight is provided to teams driving operational direction and strategic guidance for assigned portfolio initiatives.
Required Expertise
A strong background in Clinical/Preclinical, Chemistry Manufacturing Controls (CMC), with experience in Regulatory Strategy, is required. Effective leadership and communication skills are essential for success in this role.
* Prior experience as a Cross-Functional Team Lead or similar position would be beneficial but not necessary.
Comprehensive Benefits Package:
- Competitive compensation package.
(Note: This section has been shortened due to token size limitations.)