Senior Regulatory Affairs Manager
Argenta
At Argenta, we're more than a company - we're a global team, dedicated to healthier animals. We believe that when their lives are made better, we're all the better for it.
Founded in 2006, we support companies big and small to develop and manufacture health products for pets and livestock. Our trusted, innovative solutions and services cover every stage of the process, from molecule to market. We're in a unique position. We are the world's only combined contract research and contract development and manufacturing organisation (CRO/CDMO) dedicated to animal health. Our uniqueness means:- We are ambitious, growing and building a 'one team' culture, guided by our values.
- We are team players;
- We are doers;
- We are customer-centric;
- We are innovators.
Argenta is currently looking to fill the role of Senior Regulatory Affairs Manager within our CRO Americas division. About the role:
- 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, advanced degree (DVM, PhD, MS) is preferred
- 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
- Development and regulatory experience with food animal drugs is preferred but not required
- 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
Vacancy posted 3 days ago
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