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.#J-18808-Ljbffr
Cmc Regulatory Affairs Associate: Global Submissions Leader
PAREXEL
mexico, mexico
Publicado hace 7 días
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