Specialist – Regulatory Affairs (Nutritionals)
Location: Abbott Park, Illinois, United States
Employment Type: Full-Time, On-Site
Category: Regulatory Affairs – Nutrition & Healthcare
Experience Required: 2–3 years (Regulatory or related field)
About Abbott
Abbott is a global healthcare leader dedicated to helping people live healthier, fuller lives. With operations in over 160 countries and a workforce of 114,000 employees, Abbott delivers innovative healthcare solutions spanning diagnostics, medical devices, nutrition, and branded generics. Our nutrition portfolio, including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna®, supports growth, development, and healthy living across all ages worldwide.
Abbott’s culture emphasizes career development, inclusivity, and innovation, empowering employees to make a meaningful impact on global healthcare.
Role Overview
The Regulatory Affairs Specialist at Abbott Park, IL, plays a pivotal role in supporting regulatory operations for the nutritionals business. This position ensures compliance with global and local regulatory requirements, providing guidance for product development, labeling, registration, and submission processes. The specialist operates at a middle-management influence level and contributes to regulatory strategy, documentation, and compliance initiatives.
This is an on-site role requiring strong collaboration across departments, with no relocation assistance or sponsorship provided.
Key Responsibilities
Support regulatory operations and ensure compliance with Corporate, Divisional, and SOP requirements.
Maintain current registrations and submit required documentation on schedule.
Contribute to regulatory strategy development, updates, and risk-benefit analysis for regulatory compliance.
Provide regulatory input for product lifecycle planning, including labeling, advertising, and promotion.
Interpret and apply applicable regulatory requirements, guidelines, and standards.
Maintain regulatory data within electronic systems and manage documentation in support of global submissions.
Plan and organize complex project assignments, tracking milestones and timelines.
Influence and guide team members, offering mentorship and technical guidance where applicable.
Collaborate with internal teams, including quality assurance, R&D, operations, and marketing, to solve regulatory challenges.
Participate in cross-functional regulatory projects, ensuring timely and compliant deliverables.
Required Qualifications
Bachelor’s degree (or equivalent) in Science (Biology, Chemistry, Nutrition, Dietetics, Microbiology, Immunology, Medical Technology, Pharmacy, Pharmacology), Math, Engineering, or related field.
2–3 years of experience in a regulated industry (nutritionals, medical devices, pharmaceuticals). Regulatory experience is preferred but not mandatory; relevant experience in QA, R&D, operations, or scientific affairs is acceptable.
Strong verbal and written communication skills to engage with diverse stakeholders.
Attention to detail, analytical thinking, and strong organizational skills.
Ability to manage projects independently, prioritize tasks, and meet deadlines.
Proficiency in computer applications, including word processing, spreadsheets, and regulatory data systems.
Certification (RAC or equivalent) is a plus.
Preferred Qualifications
Knowledge of regulatory requirements, submission processes, advertising and labeling compliance, and agency structures.
Experience creating and managing regulatory project plans and timelines.
Ability to think analytically and solve complex regulatory challenges independently.
Demonstrated capacity to influence and mentor less experienced colleagues.
Compensation & Benefits
Base salary range: USD 60,000 – 120,000 (may vary by location and experience).
Comprehensive healthcare coverage, retirement plans with high employer contribution, and tuition reimbursement programs.
Career development opportunities within a global, innovation-driven healthcare company.
Why Abbott
Abbott fosters a culture where employees can grow professionally, contribute to life-changing healthcare solutions, and make a tangible global impact. Join Abbott to work on innovative nutrition products that improve lives across the world.
Abbott is an Equal Opportunity Employer, committed to diversity, equity, and inclusion. All qualified applicants will be considered without regard to race, color, religion, gender, sexual orientation, age, disability, or any other legally protected status.
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