Job Description
A leading biopharmaceutical firm in Mexico is looking for a Senior Regulatory Associate to manage global CMC submissions and ensure compliance with regulatory requirements. The ideal candidate will have at least 5 years of experience in CMC regulatory affairs within the biotech or pharmaceutical industry, along with strong writing skills and technical expertise. This role offers opportunities for growth within a collaborative team, focusing on shaping regulatory strategies and driving successful submissions to advance medical innovations.
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Submit ApplicationJob Details
- Location Remote, Remote
- Job Type Full-time
- Category Asuntos legales
- Posted Date July 05, 2026
- Application Deadline August 14, 2026