Senior Regulatory Affairs Specialist - Animal Health

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere.

Join a growing regulatory consulting team supporting innovative animal health products across the U.S. market.

We are seeking a seasoned Senior Regulatory Affairs Specialist
- Animal Health to provide hands‑on regulatory execution and operational support for animal health biological and pharmaceutical products. This is an exciting opportunity for a regulatory professional who enjoys working across the full product lifecycle and partnering with cross‑functional teams to deliver compliant, timely, and high‑quality regulatory outcomes.

This role will initially support the BI Vet Animal Health account, with the opportunity to expand into broader Animal Health and U.S. Regulatory consulting projects as business needs evolve.

The Senior Regulatory Affairs Specialist is responsible for supporting U.S. regulatory affairs activities across product lifecycle management, regulatory submissions, labeling, product stewardship, regulatory operations, and compliance. This role is ideal for someone who brings strong execution skills, sound regulatory judgment, and the ability to manage multiple priorities in a client‑focused environment.

You will work closely with internal and client stakeholders across Regulatory Affairs, Quality, Manufacturing, Pharmacovigilance, Supply Chain, and Commercial teams to help ensure regulatory objectives are delivered efficiently and compliantly.

• Support regulatory lifecycle activities for animal health biologics and pharmaceutical products

• Prepare, coordinate, and maintain regulatory submissions, product registrations, and related lifecycle documentation

• Support labeling strategy execution, review, and implementation activities

• Maintain accurate regulatory documentation, records, and submission tracking

• Support product stewardship and broader regulatory operations activities

• Coordinate annual reports, post‑approval changes, and ongoing compliance activities

• Partner cross‑functionally to support the timely delivery of regulatory milestones

• Provide support for additional U.S. Regulatory consulting projects as business needs grow and shift

• Support regulatory lifecycle activities for animal health biologics and pharmaceutical products

• Prepare, coordinate, and maintain regulatory submissions, product registrations, and related lifecycle documentation

• Support labeling strategy execution, review, and implementation activities

• Maintain accurate regulatory documentation, records, and submission tracking

• Support product stewardship and broader regulatory operations activities

• Coordinate annual reports, post‑approval changes, and ongoing compliance activities

• Partner cross‑functionally to support the timely delivery of regulatory milestones

• Provide support for additional U.S. Regulatory consulting projects as business needs grow and shift

• Bachelor’s degree in a scientific discipline or related field

• 5 to 10+ years of experience in regulatory affairs or regulatory operations

• Experience supporting Animal Health, biologics, vaccines, pharmaceuticals, or related regulated products

• Familiarity with USDA‑CVB and/or FDA‑CVM preferred, but not required

• Strong organizational skills with exceptional attention to detail

• Excellent written and verbal communication skills

• Proven ability to manage multiple projects, deadlines, and…