Opportunity Description
Responsibilities:
Lead the design and development of regulatory strategy and technical documents in support of global development projects.Manage resources and provide technical leadership to ensure timely delivery of regulatory activities and compliance.Represent the regulatory viewpoint on development teams and lead engagements with regulatory agencies in the EU or the USA.Develop and maintain effective relationships with global regulatory authorities and influence industry associations.Proactively identify and communicate project-specific risks and opportunities to internal stakeholders.What You Need to Succeed (minimum qualifications):
Master’s degree or higher in veterinary medicine, biologic, infectious diseases, immunology, or a related field.A minimum of 10 years of experience in the animal health industry, with direct Regulatory Affairs experience with biologics/large molecule products.<...
Full time
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