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The Senior Specialist - Regulatory Affairs at Abbott is responsible for supporting the on-market regulatory affairs department to ensure efficient and compliant business processes. This role involves executing tasks and playing a consultative role by partnering across business functions. The individual will assist in identifying data needed for product registration worldwide, prepare and submit documentation for registration, and oversee such preparation. The position is based in Lake Bluff, IL, and is part of the Transfusion Medicine regulatory team, focusing on regulatory activities required for product market entry and ongoing support.