BioSpace
Head of Global Regulatory Affairs Operations, Compliance & Process Excellence (S
BioSpace, Boston, Massachusetts, us, 02298
Head of Global Regulatory Affairs Operations, Compliance & Process Excellence (Senior Director) Join to apply for the
Head of Global Regulatory Affairs Operations, Compliance & Process Excellence (Senior Director)
role at
BioSpace
Are you ready to apply Make sure you understand all the responsibilities and tasks associated with this role before proceeding. This position is currently active and accepting applications. About the role:
The Plasma-Derived Therapies (PDT) R&D Organization focuses on developing plasma-derived therapies for patients with immunologic, hematologic, and other complex diseases. The Head of Global Regulatory Affairs Operations, Compliance & Process Excellence oversees global regulatory affairs operations for the PDT BU portfolio. Responsibilities include: Supporting global regulatory submissions and ensuring timely execution. Providing strategic leadership on regulatory compliance and process efficiencies. Managing relationships with external vendors and internal teams. Participating in leadership decisions and strategic planning. Qualifications:
Bachelor's degree or related experience, 7-10 years in regulatory affairs, management experience, and knowledge of global drug development regulations. Additional details include compensation, benefits, company culture, and application instructions.
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Head of Global Regulatory Affairs Operations, Compliance & Process Excellence (Senior Director)
role at
BioSpace
Are you ready to apply Make sure you understand all the responsibilities and tasks associated with this role before proceeding. This position is currently active and accepting applications. About the role:
The Plasma-Derived Therapies (PDT) R&D Organization focuses on developing plasma-derived therapies for patients with immunologic, hematologic, and other complex diseases. The Head of Global Regulatory Affairs Operations, Compliance & Process Excellence oversees global regulatory affairs operations for the PDT BU portfolio. Responsibilities include: Supporting global regulatory submissions and ensuring timely execution. Providing strategic leadership on regulatory compliance and process efficiencies. Managing relationships with external vendors and internal teams. Participating in leadership decisions and strategic planning. Qualifications:
Bachelor's degree or related experience, 7-10 years in regulatory affairs, management experience, and knowledge of global drug development regulations. Additional details include compensation, benefits, company culture, and application instructions.
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