Senior Regulatory Affairs – Animal Health (Remote)

Cencora, Inc.; Pennsylvania; À distance; USD 110 000 - 160 000; Plein temps

Résumé du poste

Cencora seeks a Senior Regulatory Affairs Specialist - Animal Health to join a growing regulatory consulting team and support U.S. animal health products across the lifecycle.

You will lead regulatory submissions, labeling, and lifecycle documentation while partnering with Regulatory, Quality, Manufacturing, and Commercial teams to ensure compliant, timely outcomes. The role requires a scientific degree and 5–10+ years of regulatory experience, with familiarity in USDA-CVB or FDA-CVM preferred.

Qualifications

• Bachelor’s degree in a scientific discipline or related field.
• 5–10+ 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.

Responsabilités

• 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 timely delivery of regulatory milestones.
• Provide support for additional U.S. Regulatory consulting projects as business needs grow and shift.

Connaissances

Regulatory experience

Project management

Strong communication

Independent worker

Formation

Bachelor’s degree in science

Description du poste

Cencora seeks a Senior Regulatory Affairs Specialist - Animal Health to join a growing regulatory consulting team and support U.S. animal health products across the lifecycle.

You will lead regulatory submissions, labeling, and lifecycle documentation while partnering with Regulatory, Quality, Manufacturing, and Commercial teams to ensure compliant, timely outcomes. The role requires a scientific degree and 5–10+ years of regulatory experience, with familiarity in USDA-CVB or FDA-CVM preferred.