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Sr. Regulatory Affairs Manager

Job in Geneva, Kane County, Illinois, 60134, USA
Listing for: Roquette Laisa España SA
Full Time position
Listed on 2026-07-04
Job specializations:
  • Pharmaceutical
    Regulatory Compliance Specialist, Healthcare Compliance
Salary/Wage Range or Industry Benchmark: 123372 - 125000 USD Yearly USD 123372.00 125000.00 YEAR
Job Description & How to Apply Below

Senior Manager of Regulatory Affairs – Americas

We are looking for our next Senior Manager of Regulatory Affairs – Americas.

This position is located in Geneva, IL.

Compensation

The current salary range for this role is estimated to be $ - $125,000. In addition, this position may also be eligible to earn performance‑based incentive compensation. The specific compensation offered to a candidate will be influenced by a variety of factors including but not limited to skills, qualifications, experience, and location.

What You'll Do
  • Analyze and interpret regulatory requirements applicable to food ingredients, animal feed, and industrial product lines across all Global Business Units (GBUs) of Roquette, covering United States and Canada markets. Prepare and publish regulatory submissions and supporting documentation for internal stakeholders and federal agencies to ensure compliance with applicable regulations. Draft, maintain, and update regulatory guidelines, departmental positions, and standard operating procedures (SOPs) while maintaining regulatory agency files in inspection‑ready condition to ensure compliance readiness.

    Support Regulatory Head on complex regulatory problems requiring in-depth evaluation of situations, data, and various contributing factors. Provide monitoring and analytical support to ensure internal compliance with regulatory policies and effectively communicate regulatory information to all organizational levels using strong presentation skills.

    Develop regulatory strategies in collaboration with designated teams to register novel ingredients and components for Roquette food and feed products, and assist in food product qualification processes with various regulatory agencies to ensure regulatory frameworks are properly translated into regulatory policies and implemented. Create and update regulatory systems and documentation for product and agency compliance based on current and emerging legislation, and implement tools and databases for regulatory operations and process improvements.

    Provide regulatory assessments and support for daily customer compliance requests, compile product ingredient information and regulatory assessments by country for the Americas and globally, and provide regulatory documents for food and feed products in compliance with customer and country‑specific requirements.

    Lead Generally Recognized as Safe (GRAS) affirmation processes and develop food product label claims, including Natural, GMO, and Organic product strategies in accordance with developing legislation. Influence development of new regulations and updates to existing regulations through collaboration with health authorities and trade associations to prepare the regulatory landscape for future innovations. Serve as regulatory interface between Quality, Application groups, Scientific, Legal, and Government Relations departments, and communicate internally and externally with colleagues, regulatory contacts, suppliers, and customers regarding product support and compliance matters.

    Solve complex regulatory problems and efficiently interact with colleagues, managers, and regulatory agency representatives. Domestic and international travel required up to 5% of time. Part‑time telecommuting within the area of intended employment is permitted.

What You'll Need Education
  • A Bachelor’s degree or foreign equivalent in Pharmaceutical Science or other Lifesciences or related field, plus 4 years of experience in a regulatory affairs occupation with a food ingredient, or pharma ingredient, or consumer packaged food company.
Experience

The required experience must include the following:

  • 4 years of experience in regulatory or quality compliance for food ingredients.
  • 4 years of experience in technical aspects of food or pharmaceuticals such as chemistry, pharmacology, nutrition, or similar technical activities.
  • 2 years of experience with food regulations and policy environment.

Any and all experience may be gained concurrently.

Applicant must also possess demonstrated knowledge of the following:

  • Ability to write technical reports and dossiers, including building scientific arguments to support new food and feed…
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