Job Overview
The primary role of this position is to ensure seamless regulatory compliance and efficient project coordination.
* Assist in the management and organization of regulatory activities for post-approval submissions, focusing on labeling changes, and create supporting documentation.
* Guarantee timely submission of suitable post-approval documents according to established company procedures.
About Your Qualifications & Skills
We seek a candidate with an effective combination of the following qualifications, skills, and experiences:
* Bachelor's degree in Life Sciences or a related field.
* Prior experience in Regulatory Affairs.
* Excellent communication and writing skills.