Description
The role is a Regulatory Affairs Specialist focused on CMC regulatory strategy, registration, health-authority liaison, post-marketing authorization compliance, regulatory documentation, and regulatory intelligence. It requires a Bac + 5 in a scientific or quality-related field or a Doctor of Pharmacy/Master's in Regulatory Affairs, at least five years of pharmaceutical industry experience including Regulatory Affairs and preferably CMC, and fluent English. The position is on a permanent contract, primarily based in Les Ulis with a remote-work agreement of up to two days per week after four months, and offers health insurance and other benefits.
