Regulatory Affairs Manager - Feed Enzymes

Kemin; Des Moines (IA); On-site; USD 70,000 - 110,000; Full time

Job summary

An established industry player is seeking a Regulatory Affairs Manager to join their Animal Nutrition and Health team. This pivotal role involves preparing and submitting regulatory dossiers for enzyme products used in animal feed across North America. The ideal candidate will possess extensive experience in regulatory affairs, particularly with the FDA and CFIA, and will be responsible for interpreting scientific data, collaborating with various departments, and ensuring compliance with government regulations. This position offers a dynamic environment where your expertise will directly contribute to the commercialization of innovative products that enhance animal nutrition and health. If you are passionate about regulatory affairs and thrive in a fast-paced setting, this is the opportunity for you.

Qualifications

• 7+ years of experience in regulatory affairs for feed enzymes.
• Strong communication and project management skills are essential.

Responsibilities

• Prepare and submit regulatory dossiers for feed enzymes.
• Collaborate with internal departments to ensure compliance.

Skills

Regulatory Affairs

Project Management

Communication Skills

Analytical Abilities

Customer Service Orientation

Education

Bachelor's Degree in a Science related field

Tools

Microsoft Office

Job description

Overview

We're hiring! Kemin is seeking a Regulatory Affairs Manager to join our Animal Nutrition and Health team. This position is responsible for preparing and submitting dossiers to support registration of enzyme products used in animal feed in the United States, Canada, Mexico, and/or Central America.

The ideal candidate will have experience successfully registering feed enzymes in the United States. Candidates with lesser experience may be considered for a commensurate role.

Responsibilities

• Review and interpret scientific data supporting safety and efficacy of feed enzymes to prepare dossiers to support regulatory approval for a variety of non-GMO and GMO enzymes used in livestock feed.
• Interpret relevant government regulations and determine regulatory requirements to prepare dossiers for government approval of various feed enzyme products.
• Prepare and submit dossiers for a variety of feed enzymes to regulatory agencies in North America, not limited to FDA and CFIA.
• Develop and utilize regulatory strategies to achieve product registrations for feed enzymes on a timely basis to support commercialization efforts.
• Serve as a Kemin regulatory feed enzyme expert under the direction of senior Regulatory Affairs management.
• Collaborate and communicate with other internal departments such as, but not limited to R&D, Marketing, Sales, Technical Services, Finance, and Leadership team members.
• Responsible for review of enzyme product formulations, product claims, labels, and associated marketing and sales collateral.
• Attend industry meetings or trade shows when necessary; stay current on trends as they affect feed enzyme regulations.

Qualifications

• Education and Experience:
  • Bachelor's Degree in a Science related field with a minimum of 7+ years of demonstrated experience in successfully preparing dossiers and registering enzymes used in animal feed with the FDA and CFIA.
• Must be customer service oriented and work well with varied personalities inside and outside of Kemin.
• Strong written and oral communication skills.
• Ability to read, write, and handle basic math problems.
• Ability to manage projects while working in a fast-paced business environment.
• Analytical abilities.
• Extensive knowledge of Microsoft Office software.
• Up to 5% travel.

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

Kemin is an equal opportunity employer, and all reasonable accommodations will be considered.

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