Sr. Regulatory Affairs Specialist

Overview

Hennessy Research Associates - a Kemin company is seeking a detail-oriented and experienced Regulatory Affairs Senior Specialist to join our Animal Health Biologics team. In this role, you will be responsible for preparing regulatory submission to U.S. Department of Agriculture (USDA) Center for Veterinary Biologics (CVB) regulations and dossiers for International registration. The position is primarily focused on licensing biologics for veterinary use.

This is an excellent opportunity for a regulatory professional who has experience with veterinary biologics regulatory affairs, is passionate about animal health and enjoys working in a fast-paced, science-driven environment.

This position will work on-site at Hennessy Research Associates located in Lexexa, Kansas

Join the Kemin Team and Transform Lives!

We are a privately held, family-owned-and-operated global biotechnology company driven by curiosity and committed to transforming the quality of life for people, pets, and the planet.

We create solutions that strengthen health and wellbeing, provide nutrition and immune support for pets and production animals, safeguard the planet’s natural resources, and protect the global food supply chain for generations to come.

We supply over 500 specialty ingredients for various industries, including human and animal health and nutrition, pet food, aquaculture, nutraceutical, food technologies, crop technologies, textiles, biofuels, and animal vaccines.

We employ 3,500 global employees and operations in 90 countries, including manufacturing facilities in Belgium, Brazil, China, Egypt, India, Italy, San Marino, Singapore, South Africa, and the United States.

Benefits

As a valued member of our team, you'll enjoy a comprehensive benefits package designed to support your financial, physical, and professional well-being:

• Competitive Financial Package: Enjoy a rewarding salary, uncapped bonus opportunities, a 401k match program, and generous paid vacation and holidays.
• Career Development and Advancement: Unlock your potential with opportunities for growth and development throughout your entire career.
• Continued Learning Opportunities: Grow your skills with our in-house learning platforms, offering thousands of training resources both live and online, and take advantage of tuition reimbursement for external post-secondary pursuits.
• Service Opportunities: Make a positive impact with paid time off for volunteering in your community
  
  

Responsibilities

• Prepare, compile, and submit registration documents for new product licensure to the USDA Center for Veterinary Biologics (CVB).
• Ensure documents and studies are compliant with USDA regulations (9 CFR) and maintain up-to-date product licenses, outlines of production, and labeling.
• Develop appropriate regulatory strategy and monitoring to provide efficient licensing of new products.
• Participate and potentially lead cross-functional project teams to support product development from early-stage research through commercialization.
• Monitor and interpret evolving regulatory requirements and communicate relevant updates to internal stakeholders.
• Serve as a liaison between internal departments (R&D, QA/QC, Manufacturing, Marketing) and regulatory agencies.
• Coordinate regulatory submissions and communications for international markets as needed.
• Maintain accurate records and regulatory documentation in compliance with company and regulatory agency standards.
• Support regulatory inspections and audits by USDA or international authorities.
• Identify and mitigate regulatory risks in collaboration with research and development, quality and production teams.
  
  

Qualifications

• Bachelor’s degree in life science field (e.g., biology, microbiology, veterinary science, biochemistry).
• 2–5 years of experience in regulatory affairs with a focus on veterinary biologics.
• Strong knowledge of USDA-CVB regulatory requirements and 9 CFR.
• Experience preparing and submitting regulatory documents to USDA and responding to agency inquiries.
• Excellent written and verbal communication skills.
• Strong organizational skills and attention to detail.
• Proficient in Microsoft Office and electronic document management systems.
• Ability to travel on occasion for off-site meetings and training. No more than 10%
  
  

Preferred

• Graduate degree in life sciences, with focus on microbiology, immunology, veterinary science or related degree.
• Experience with International registrations
• Some proficiency in a second language, such as Spanish, French or Arabic
  
  

We are an equal opportunity employer. We consider all qualified applicants without regard to race, color, creed/religion, national origin, ancestry, citizenship or immigration status (where applicable), sex, sexual orientation, gender identity or expression, pregnancy/childbirth/breastfeeding or related conditions, age (40 ), disability (including the use of a service animal), genetic information, marital status, familial or caregiver status, military or veteran status, status as a victim of domestic violence, reproductive health decision‑making, and any other status protected by applicable federal, state, or local law. We also prohibit retaliation for raising concerns or participating in an EEO process. Applicants who need a reasonable accommodation to apply or interview can email TalentAcquisition.US@Kemin.com .

A post-offer background check and drug screen is required. Additional pre-employment requirements may be necessary based on position.

Kemin is a drug-free and tobacco-free campus.