Regulatory Affairs (CMC)
Senior Director, Regulatory Affairs CMC
Hurley Consulting is looking for a Regulatory Affairs professional. A Master's Degree or advanced degree preferred with at least 7+ experience in areas such as R&D, CMC and Quality Assurance in the pharmaceutical industry.
The responsibility will include:
Prepare or review Regulatory/CMC technical documents, CTD Module 2, 3 and Module 3 for submissions.
Review of CTD Module 2.3 and Module 3 for technical content and compliance with regulatory requirements.
Manage novel compound contract manufacturing for drug substances and drug products
Knowledge of CMC, FDA, EMA and ICH guidelines.
Experience with IND preparation and IND amendments, NDA submissions and supplements and CTD format and electronic submissions.
Experience in management of multiple projects.
Analytical chemistry experience a plus.
Hurley Consulting Associates Ltd. offers a competitive salary, health care benefits, group life insurance and 401(k) plan. Remote (optional).