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Kemin

Global supplier of specialty ingredients.

RA Associate - Registration Specialist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeDes Moines, IA, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in a science-related field and 3–5 years of related experience are required.
  • Extensive knowledge of Microsoft Excel, Word, and PowerPoint is required.
  • Experience with FDA Center of Veterinary Medicine registrations, reviews, and procedures is required.
  • Fluency in English is required.
  • Familiarity with regulations in the region is required.
  • Attention to detail, reliability, motivation, and the ability to work independently and interact well in a team environment are required.
  • Verbal, written, interpersonal communication, technical writing, and presentation skills are required.
  • Organizational and time-management skills, including prioritizing, planning, and project management, are required.
  • Experience reviewing and evaluating scientific literature and analyzing and synthesizing scientific information from multiple sources, including identifying information gaps and future research needs, is required.
  • Ability to travel up to 10% is required.

Responsibilities

  • Prepare registration dossiers, amendments, monthly reports, and supplements for submission to regulatory authorities with limited supervision.
  • Review departmental standard operating procedures and recommend changes.
  • Provide input to support assessments of changes to manufacturing and testing facilities for the market.
  • Represent Regulatory Affairs on team projects under limited supervision as knowledge grows.
  • Understand regional regulatory requirements and relevant government regulations, and stay current on regulatory issues affecting Kemin products in those countries.
  • Evaluate and research submission deficiencies, additional information requests, or testing requested by regulatory authorities.
  • Follow and maintain a food and feed safety environment in compliance with applicable rules and regulations.
  • Serve as a Kemin liaison to major regulatory agencies and participate in government agency inspections, including those involving the FDA, CFIA, USDA, OSHA, DOT, and FAA, as needed.

Desired Qualifications

  • Additional language proficiency is a plus.

About the Company

Kemin

Global supplier of specialty ingredients.

Kemin is a global ingredient manufacturer that supplies more than 500 specialty ingredients for human health, food safety, and protecting the world’s food supply. Its ingredients are produced and delivered for use across industries such as animal health, nutraceuticals, pet food, crop technologies, aquaculture, textiles, and vaccines, helping improve health and safeguard food systems. The company differentiates itself with its privately held, family-owned structure, long history since 1961, and a broad, 120+-country footprint supporting a diversified product portfolio. Its goal is to sustainably transform the quality of life for 80 percent of the world every day through its ingredients and services, while ensuring quality, safety, and efficacy.

Company size
1,001-5,000
Company stage
Debt Financing
Total funding
$115M
Headquarters
Des Moines, IA
Founded
1961

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