Regulatory Affairs Intern at Phibro Animal Health | Apply Now
Regulatory Affairs Intern opportunities are highly valuable for students and graduates interested in animal health, regulatory science, and FDA submission processes. Phibro Animal Health is currently offering a remote internship in the United States, providing hands-on experience in regulatory affairs, animal health product development, dossier assessment, study oversight, and regulatory operations. This role is ideal for candidates seeking practical exposure to regulatory pathways within a leading global animal health company.
- Job Position: Regulatory Affairs Intern
- Company Name: Phibro Animal Health Corporation
- Division: Animal Health & Nutrition
- Department: Regulatory Affairs
- Job Location: Teaneck, New Jersey, United States – Remote
About Phibro Animal Health
Phibro Animal Health Corporation is a publicly traded global company with a rich history in animal health and nutrition. The company manufactures and markets medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition solutions. Phibro works closely with livestock producers, farmers, veterinarians, and consumers to support animal health and well-being.
In addition to animal health products, Phibro is involved in manufacturing and marketing products for ethanol performance, plant microbials, home and industrial applications, and specialty chemicals. The company generates annual revenues exceeding $1 billion and employs more than 2,400 professionals worldwide. Phibro Animal Health is committed to building a diverse workforce where employees are encouraged to share their creativity, skills, and expertise in a supportive environment.
Regulatory Affairs Intern Description
Regulatory Affairs Intern candidates will support the Animal Health Regulatory Affairs team by learning regulatory pathways and sponsor obligations associated with new animal drug development and approval processes.
This internship provides practical exposure to regulatory strategy, dossier assessments, study oversight requirements, procedural document writing, and document organization activities that support future system migration projects. The role is designed for individuals interested in regulatory science, animal health product development, FDA submission processes, and regulatory operations.
Qualifications
Regulatory Affairs Intern applicants should meet the following educational requirements:
Currently pursuing a Bachelor’s, Master’s, or Professional Degree in:
- Animal Science
- Biological Sciences
- Regulatory Affairs
- Related Scientific Disciplines
Preferred
- Strong interest in animal health product development
- Interest in regulatory science and FDA submission processes
- Ability to analyze scientific and regulatory information
- Excellent written communication skills
Physical Requirements
- Good hand-eye coordination
- Frequent ability to talk and hear
- Ability to perform routine office and documentation tasks
Key Responsibilities
- Learn the regulatory framework for new animal drug approvals, including submission requirements and health authority expectations.
- Review and summarize dossier content, technical data, and supporting documentation.
- Assist with background research related to MUMS criteria.
- Support understanding of sponsor obligations for nonclinical and clinical studies conducted under GLP and GCP principles.
- Draft, revise, and format procedures, work instructions, and controlled documents related to regulatory operations.
- Organize, index, and maintain FDA regulatory correspondence and records.
- Support retrieval activities, inspection readiness, and future migration into Veeva systems.
- Collaborate with Regulatory Affairs and cross-functional teams to gather information and support project deliverables.
Required Skills
- Proficiency in Microsoft Office Products
- Strong written and verbal communication skills
- Ability to work independently and within teams
- Excellent customer service orientation
- Strong organizational and documentation abilities
- Ability to summarize complex scientific and regulatory information clearly and accurately
Why Apply for This Regulatory Affairs Intern Role?
Regulatory Affairs Intern opportunities at Phibro Animal Health offer aspiring regulatory professionals a chance to gain practical experience in animal health product development, FDA regulatory processes, dossier review, regulatory documentation, and study oversight. This remote job in the US provides valuable exposure to regulatory affairs within a globally recognized animal health company.
