Key skills
R
About this role
Role Overview
- Ensure timely approval of nutritional products for EURI region
- Direct development of product registration dossiers and submissions
- Lead regulatory submissions strategy
- Maintain regulatory data in electronic systems
- Collaborate with affiliates to support regulatory agency interactions
- Advise project teams on manufacturing changes and technical labeling
- Assist in SOP development and review
Requirements
- Bachelor's degree (or equivalent) in science, math, engineering, or medical fields
- M.S. in a technical area is preferred
- Certification such as RAC from the Regulatory Affairs Professionals Society is a plus
- 2-3 years of experience in regulatory preferred, but may consider quality assurance, R&D, scientific affairs, operations
- 3-4 years of experience in a regulated industry (e.g., nutritionals, medical products)
- Knowledge of regulatory requirements, guidelines, and GxPs
- Experience with RIMS (systems) for submission dossier management
- Strong attention to detail
Benefits
- Training and career development
- Onboarding programs for new employees
- Tuition assistance
- Financial security through competitive compensation
- Incentives and retirement plans
- Health care and well-being programs