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Regulatory Affairs Manager

DeLaval

Des Plaines (IL)

Hybrid

USD 100,000 - 120,000

Full time

26 days ago

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Job summary

DeLaval is seeking a Regulatory Affairs Manager to support product registrations and ensure compliance in North America. This role involves collaboration with cross-functional teams and managing regulatory submissions for veterinary pharmaceuticals, affecting food safety and animal health.

Benefits

Competitive compensation and benefits package
Hybrid work flexibility
Opportunities for professional development and global collaboration

Qualifications

  • 5+ years of regulatory affairs experience in veterinary pharmaceuticals or disinfectants.
  • Strong knowledge of US EPA, FDA, and Health Canada regulations.

Responsibilities

  • Lead and maintain product registrations with US EPA, FDA, and Health Canada.
  • Serve as liaison with regulatory authorities for veterinary drugs.

Skills

Regulatory Affairs
Communication
Team Management

Education

Master’s degree in Chemistry, Biochemistry, Toxicology, or related field

Tools

Microsoft Office

Job description

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Regulatory Manager– North America

Des Plaines/Kansas City | Hybrid Work Model Available

Regulatory Manager– North America

Des Plaines/Kansas City | Hybrid Work Model Available

About DeLaval

DeLaval is a global leader in dairy farming innovation, delivering integrated milking and hygiene solutions that enhance productivity, animal welfare, and sustainability. With over 125 years of heritage and a presence in more than 100 markets, we are committed to shaping the future of food production. As part of the Tetra Laval Group, we combine tradition with cutting-edge science to support millions of dairy farmers worldwide.

Why Join Us?

At DeLaval, you’ll be part of a purpose-driven team that values innovation, collaboration, and continuous learning. We offer a dynamic work environment where your expertise in regulatory affairs will directly impact food safety, animal health, and environmental stewardship.

Your Role: Regulatory Manager – Milk Quality & Animal Health (MQAH)

As a Regulatory Manager you will play a pivotal role in ensuring compliance and driving product registrations across North America. Reporting to the Director of Regulatory Affairs, you will collaborate with cross-functional teams including R&D, Product Management, and Quality Assurance to support a diverse portfolio of veterinary pharmaceuticals and sanitizing agents. The incumbent of this position will be responsible for tracking the progress of all activities of the team as well as monitoring current developments in the regulatory field for North America.

Key Responsibilities

  • Lead and maintain product registrations with US EPA, FDA, and Health Canada, including renewals, amendments, and new submissions.
  • Serve as the primary liaison with regulatory authorities and consultants for veterinary drugs and disinfectants in both US and Canada.
  • Evaluate and approve production documentation, including formulations, raw material specs, and test methods.
  • Review protocols and final reports to support regulatory submissions.
  • Ensure compliance of product labels and marketing materials with federal and state regulations in both US and Canada.
  • Maintain FDA drug listings and manage Food Contact Notifications for R&D initiatives.
  • Develop and update Safety Data Sheets (SDS) in accordance with GHS standards.
  • Monitor regulatory changes and proactively communicate compliance strategies to internal stakeholders.

What You Bring

  • Master’s degree in Chemistry, Biochemistry, Toxicology, or related field; coursework in Animal Science is a plus.
  • 5+ years of regulatory affairs experience in veterinary pharmaceuticals, disinfectants, or related industries.
  • Strong knowledge of US EPA (FIFRA), FDA (animal drugs and food contact), and Health Canada regulations.
  • Experience with ISO, GLP, and GMP environments preferred.
  • Excellent communication skills and the ability to manage multiple priorities in a fast-paced setting.
  • Proficiency in Microsoft Office and regulatory databases.
  • Stable leadership of a small team.
  • Willingness to travel up to 10%.

Preferred Qualifications

  • Experience in dairy production or in-vitro testing.
  • Demonstrated ability to work independently and influence cross-functional teams.
  • Hands-on mentality as well as experience in leading teams, coaching and managing administrative processes.

What We Offer

  • Competitive compensation and benefits package.
  • Hybrid work flexibility.
  • Opportunities for professional development and global collaboration.
  • A mission-driven culture focused on sustainability and innovation.

Ready to Make an Impact?

Apply now via the DeLaval Job Portal and join us in advancing the future of dairy farming.

Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Legal
  • Industries
    Food and Beverage Manufacturing

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