QIAGEN is seeking a Senior Specialist Regulatory Affairs in Mexico City to ensure compliance and lifecycle management of IVD and medical device products.
You will collaborate with teams like Quality, Operations, and Marketing while engaging with regulatory authorities.Your tasks include managing regulatory submissions, ensuring accuracy and compliance, and acting as a key contact for COFEPRIS.
The role requires a degree in life sciences and experience in regulatory affairs.We offer bonuses, local benefits, and a hybrid work model.
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