Amerisource Bergen

Senior Manager, Regulatory Affairs – Animal Health Labeling

Amerisource Bergen • $76K — $119K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s degree in a scientific, regulatory, veterinary, pharmaceutical, or related discipline.
  • Significant regulatory affairs experience with pharmaceuticals, biologics, vaccines, or animal health products.
  • Demonstrated experience in product labeling and regulatory submissions.
  • Strong knowledge of labeling compliance and regulatory documentation.
  • Ability to provide independent regulatory guidance and manage competing priorities.
  • Excellent written and verbal communication skills with strong stakeholder-management experience.
  • Experience in client-facing and cross-functional roles.

Responsibilities

  • Manage labeling activities for animal health products throughout their lifecycle.
  • Develop regulatory labeling strategies to ensure compliance and achieve commercial goals.
  • Prepare and coordinate labeling submissions to regulatory bodies like FDA-CVM and USDA-CVB.
  • Support creation and review of various labeling components such as package inserts and promotional labeling.
  • Lead the regulatory approval process for labeling and artwork changes.
  • Review labeling content for compliance and alignment with regulations.
  • Serve as a contact for regulatory inquiries and monitor submission milestones.

Benefits

  • Medical, dental, and vision care coverage.
  • Support for working families, including dependent care, adoption assistance, and infertility coverage.
  • Comprehensive behavioral health solutions and paid parental leave.
  • Training and professional development resources available.
  • Opportunities for mentorship and participation in employee groups.
Full Job Description

The Senior Manager, Regulatory Affairs – Animal Health Labeling provides regulatory leadership and hands-on execution for U.S. animal health pharmaceutical and biological products. This client-facing role supports labeling and Regulatory Operations activities throughout the product lifecycle, develops regulatory strategies, prepares and coordinates submissions, and supports compliant implementation and maintenance of approved labeling.

The position works closely with Regulatory Affairs, Quality, Manufacturing, Marketing, Supply Chain, Pharmacovigilance, and other cross-functional stakeholders.


Responsibilities

  • Manage labeling activities for animal health pharmaceutical and biological products throughout the product lifecycle.
  • Develop and implement regulatory labeling strategies supporting compliance, product maintenance, and commercial objectives.
  • Prepare and coordinate labeling submissions to FDA Center for Veterinary Medicine and USDA Center for Veterinary Biologics.
  • Support labeling components including container labels, cartons, package inserts/product circulars, administration/use instructions, shipper labels, and applicable promotional labeling.
  • Lead labeling and artwork changes from initiation and regulatory assessment through approval, implementation, and archival.
  • Review labeling content for regulatory compliance, consistency, and alignment with approved applications.
  • Prepare submission summaries, justifications, summaries of changes, annotated labeling, artwork components, and supporting documentation.
  • Support electronic submission activities using systems such as Veeva Vault, eSubmitter, and the USDA NCAH Portal.
  • Serve as a regulatory point of contact for health-authority inquiries, deficiencies, commitments, and approvals.
  • Track submission milestones, agency feedback, implementation requirements, and labeling histories.
  • Assess proposed labeling changes and determine appropriate regulatory strategies and reporting categories.
  • Support lifecycle activities, including safety updates, manufacturing changes, product line extensions, market expansion, and product discontinuation.
  • Provide regulatory labeling guidance and technical support to cross-functional teams.
  • Monitor emerging regulations and identify opportunities to improve labeling processes and submission efficiency.
  • Support additional U.S. regulatory programs and client engagements as business needs evolve.

#LI-AT2

Required Qualifications

  • Bachelor’s degree in a scientific, regulatory, veterinary, pharmaceutical, or related discipline.
  • Significant regulatory affairs experience supporting pharmaceuticals, biologics, vaccines, animal health products, or related regulated products.
  • Demonstrated experience with product labeling, regulatory submissions, and lifecycle management.
  • Strong knowledge of labeling compliance, artwork change control, and regulatory documentation.
  • Ability to work independently, manage competing priorities, and provide confident regulatory guidance.
  • Strong written and verbal communication, organization, and stakeholder-management skills.
  • Experience working effectively in a client-facing and cross-functional environment.

Preferred Qualifications

  • Ten or more years of relevant regulatory affairs experience.
  • Direct experience with animal health pharmaceutical and biological products.
  • Experience preparing submissions for FDA-CVM and USDA-CVB.
  • Experience with Veeva Vault, eSubmitter, and the USDA NCAH Portal.
  • Experience communicating directly with U.S. health authorities.
  • Experience providing technical leadership, training, or mentoring within regulatory teams.

What Cencora offers

We provide compensation, benefits, and resources that enable a highly inclusive culture and support our team members’ ability to live with purpose every day. In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness. This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave. To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more. For details, visit

Full time

Salary Range*

$76,200 - 119,460

*This Salary Range reflects a National Average for this job. The actual range may vary based on your locale. Ranges in Colorado/California/Washington/NewYork/Hawaii/Vermont/Minnesota/Massachusetts/Illinois State-specific locations may be up to 10% lower than the minimum salary range, and 12% higher than the maximum salary range.

About Amerisource Bergen

AmerisourceBergen Corporation is a pharmaceutical distribution company headquartered in Chesterbrook, Pennsylvania. It was founded in 2001 through the merger of AmeriSource Health Corporation and Bergen Brunswig Corporation. The company distributes a wide range of pharmaceutical products, including brand-name and generic drugs, specialty drugs, and over-the-counter medications. AmerisourceBergen serves healthcare providers, including hospitals, pharmacies, and physician practices, as well as pharmaceutical manufacturers. The company is committed to sustainability and has implemented several initiatives to reduce its environmental impact.
Learn more about Amerisource Bergen
Size
21,000 employees
Industry

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