Senior Regulatory Affairs Specialist – Animal Health

Cencora

Senior Regulatory Affairs Specialist providing hands-on regulatory execution and operational support for animal health products in the U.S. Collaborating with cross-functional teams to achieve regulatory milestones.

Posted 7/31/2026full-timeRemote • Pennsylvania • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in regulatory lifecycle activities for animal health biologics and pharmaceuticals, with a strong focus on regulatory submissions, compliance, and cross-functional collaboration. Proven ability to manage multiple projects while maintaining meticulous documentation and communication.

Highest-signal resume keywords

Regulatory Affairs ExperienceAnimal Health ExpertiseRegulatory Submissions ManagementProject Management SkillsCross-Functional Collaboration

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Regulatory SubmissionsProduct RegistrationsLifecycle DocumentationCompliance ActivitiesLabeling Strategy ExecutionUSDA-CVB FamiliarityFDA-CVM Familiarity

Soft Skills

Strong Organizational SkillsAttention to DetailExcellent Written CommunicationExcellent Verbal CommunicationAbility to Manage Competing Priorities

Industry Keywords

Animal HealthBiologicsPharmaceuticalsVaccinesRegulated Products

About the role

Key responsibilities & impact

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

Requirements

What you’ll need

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 competing priorities
Ability to work independently while collaborating effectively with cross-functional teams

Benefits

Comp & perks

Health insurance
401(k) matching
Flexible work hours
Paid time off
Remote work options
Backup dependent care
Adoption assistance
Infertility coverage
Family building support
Behavioral health solutions
Paid parental leave
Paid caregiver leave
Training programs
Professional development resources
Mentorship programs
Employee resource groups
Volunteer activities