Regulatory Affairs Expert

2 days ago


Boston, Massachusetts, United States ArkeaBio Full time
Job Summary

The Regulatory Affairs Specialist at ArkeaBio will be responsible for preparing and reviewing regulatory documents for a novel veterinary product across multiple international jurisdictions. This role requires a strong understanding of regulatory requirements, excellent organizational skills, and the ability to work independently while collaborating with internal teams and external consultants.

This is a US-based role that offers a flexible work environment and unlimited paid time off. The successful candidate must be eligible to work in the US and have a minimum of 8-10 years experience in regulatory affairs, preferably related to veterinary products.

  • Prepare and review regulatory documents for novel veterinary product applications, ensuring compliance with each region's regulations.
  • Develop regulatory strategies to facilitate timely approvals and optimize submission processes, working in consultation with external consultants who are experts in their respective jurisdictions.

ArkeaBio is committed to diversity, equity, and inclusion, and our culture promotes an inclusive work environment. We offer a competitive salary range of $120,000 - $150,000 per year, depending on experience, and a comprehensive benefits package, including health insurance and a 401(k) matching program.

We are seeking a highly motivated and detail-oriented individual who can effectively manage parallel jurisdictional submission timelines and communicate with regulatory authorities as necessary.

About ArkeaBio

ArkeaBio is a leading biotechnology company dedicated to developing innovative veterinary products. Our team is passionate about creating a better future for animals and people alike. As a Regulatory Affairs Specialist, you will play a critical role in bringing our products to market while ensuring compliance with regulatory requirements.



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