Senior Regulatory Affairs Manager

• Facilitates and supports the regulatory and drug development requirements of external clients and internal projects
• Effectively manage client and stakeholder expectations by providing timely, relevant, and accurate documents, assessments, reports and communications
• Demonstrates an awareness of current regulations, guidance's, regulatory processes, and the animal drug development process, while maintaining a flexible and creative mindset to work through regulatory challenges
• Creates regulatory solutions to complex issues
• Provides client accurate expert regulatory advice on animal health product development
• Represent Argenta in industry associations (e.g. GADA, AHI, SQA)
• Identify and pursue new regulatory consulting opportunities which may include meeting with new clients, traveling and speaking at professional meetings, networking in the industry and contributing to various publications

• Bachelor’s degree or equivalent experience in a scientific discipline
• 8+ years experience in veterinary regulatory and/or animal drug development
• Proven experience includes several of the following: CVM, E-Submitter, GLP, GCP, GMP, USDA, EPA, EMA
• Good written and oral communication skills, and ability to work collaboratively within and across teams
• Results and bottom line oriented
• Excellent analytical skills and attention to detail
• Proven influence, negotiation and persuasion skills
• Defines and plans priorities well. Comfortable balancing shifting priorities as required to meet business needs

Advanced degree (DVM, PhD, MS) is preferred