Senior Scientific & Regulatory Affairs Manager – Global Food Ingredient Compliance & Risk Assessment (Remote – Boca Raton, FL)

Why Intertek? A Global Leader in Quality, Safety & Sustainability

Intertek is a world‑renowned Total Quality Assurance (TQA) provider, operating in the $250 billion quality‑assurance market. With more than 1,000 laboratories and offices across 100+ countries, we partner with leading food, nutrition, pharmaceutical, industrial, and consumer brands to ensure their products meet the highest standards of safety, compliance, and sustainability. Our Health, Environmental & Regulatory Services (HERS) business line is at the forefront of scientific, toxicological, and regulatory expertise, delivering customized solutions that protect public health and strengthen supply‑chain resilience.

At Intertek, we live by a purpose‑driven culture: making the world a safer, more sustainable place for all. Our employees are empowered to innovate, collaborate across borders, and shape the future of global food safety. If you thrive in a fast‑paced, intellectually curious environment and want to make a tangible impact on the foods we all eat, you’ve found the right place.

Position Overview – Senior Scientific & Regulatory Affairs Manager (Remote)

We are seeking an experienced, client‑focused senior professional to lead our Food Ingredient Compliance & Risk Assessment practice. As a Senior Scientific & Regulatory Affairs Manager, you will act as a trusted advisor to our multinational clients, guiding them through the complex landscape of FDA, EU, Canadian, and other worldwide regulations. You will serve as a program manager for high‑visibility projects, drive new business development, and mentor a talented team of regulatory specialists.

This role is fully remote, with a home‑office base in Boca Raton, FL, and offers the flexibility to work from anywhere in the United States while collaborating with a global network of experts.

Key Responsibilities – What You’ll Do Every Day

• Strategic Client Engagement: Build and nurture long‑term relationships with food manufacturers, ingredient suppliers, and nutrition brands, acting as the primary point of contact for all regulatory matters.
• Regulatory Project Leadership: Oversee end‑to‑end submission processes for GRAS (Generally Recognized As Safe) dossiers, novel food applications, food additive petitions, and dietary supplement ingredient notifications.
• Risk Assessment Development: Design, execute, and document evidence‑based toxicology and risk‑assessment frameworks for new and existing ingredients, ensuring scientific rigor and regulatory compliance.
• Global Regulatory Intelligence: Monitor FDA, EFSA, Health Canada, FSANZ, and other jurisdictional updates; disseminate actionable insights to internal teams and clients.
• Business Development: Identify new market opportunities, pitch Intertek’s consulting services, and convert prospects into revenue‑generating projects.
• Team Mentorship & Training: Lead, coach, and develop a multidisciplinary regulatory affairs team, fostering a culture of continuous learning and high performance.
• Cross‑Functional Collaboration: Partner with scientists, engineers, legal counsel, and business development colleagues to deliver integrated solutions that meet client objectives.
• Documentation & Review: Author, edit, and critically review technical and regulatory documents, ensuring clarity, accuracy, and compliance with submission standards.
• Financial Stewardship: Manage project budgets, forecast revenue, and meet or exceed profitability targets.
• Regulatory Representation: Act as Intertek’s subject‑matter expert during agency interactions, public hearings, and industry association meetings.

Essential Qualifications – What You Must Bring

• Education: B.S., M.S., Ph.D., or J.D. in regulatory science, toxicology, molecular biology, food science, or a related discipline.
• Experience: 7‑10 + years of progressive responsibility in regulatory affairs within the food, nutrition, or related industries.
• Regulatory Expertise: Deep knowledge of U.S. FDA food safety frameworks (GRAS, FSMA, food additive petitions) and solid familiarity with EU, Canadian, and ANZ regulatory systems.
• Submission Success Record: Proven ability to lead successful GRAS panels, novel food approvals, and additive petitions on schedule and within budget.
• Risk Assessment Skills: Demonstrated experience applying toxicological data, exposure assessments, and scientific literature to build robust safety dossiers.
• Communication Excellence: Superior oral and written communication skills, with the ability to translate complex scientific concepts for diverse audiences.
• Project Management: Strong organizational capabilities, attention to detail, and proven track record of delivering multi‑disciplinary projects on time.
• Networking Proficiency: Established relationships with regulatory agencies, industry groups, and key opinion leaders.
• Self‑Motivation & Remote Work Discipline: Ability to thrive in a remote environment, manage priorities independently, and stay accountable.

Preferred Qualifications – Nice-to‑Have Extras

• Experience with international regulatory harmonization initiatives (e.g., Codex Alimentarius).
• Prior experience leading virtual, globally dispersed teams.
• Familiarity with regulatory software platforms (e.g., RegDesk, Veeva Vault).
• Certified Project Management Professional (PMP) or equivalent credential.
• Published research or conference presentations in food safety or toxicology.

Core Competencies & Skills – The DNA of Success

• Analytical Thinking: Ability to dissect complex data sets, identify trends, and derive actionable regulatory strategies.
• Strategic Vision: Forward‑looking mindset that anticipates future regulatory shifts and positions clients for long‑term compliance.
• Leadership Presence: Inspire confidence, provide clear direction, and empower team members to excel.
• Negotiation & Influence: Persuasive communicator who can secure stakeholder buy‑in and resolve regulatory challenges.
• Adaptability: Comfortable navigating ambiguous situations, shifting priorities, and emerging scientific evidence.
• Ethical Integrity: Commitment to upholding the highest standards of honesty, confidentiality, and professional conduct.

Career Growth & Learning – Your Future at Intertek

Intertek invests heavily in talent development. As a Senior Scientific & Regulatory Affairs Manager, you will have access to:

• Professional Development Budget: Annual allowance for conferences, certifications, and advanced coursework.
• Mentorship Programs: Pairing with senior leaders across the HERS network to broaden your expertise.
• Global Rotation Opportunities: Short‑term assignments at international labs or client sites to deepen cross‑cultural competence.
• Leadership Pathways: Clear promotion tracks to Director, Vice President, and Executive‑level roles within Intertek’s regulatory practice.
• Innovation Labs: Participate in cutting‑edge research projects on emerging food safety technologies (e.g., AI‑driven risk modeling).

Compensation, Perks & Benefits – What We Offer

While exact figures are tailored to experience and market benchmarks, you can expect a highly competitive total‑salary package that includes:

• Base salary positioned within the top quartile for senior regulatory roles in the United States.
• Performance‑based annual bonus tied to individual and company objectives.
• Comprehensive health suite – medical, dental, vision, life, and disability insurance.
• Retirement savings plan with generous company match (401(k)).
• Paid time off, parental leave, and flexible work‑schedule policies.
• Tuition reimbursement for advanced degrees or relevant certifications.
• Employee Assistance Program (EAP) and mental‑wellness resources.
• Remote‑work stipend for home‑office setup, high‑speed internet, and ergonomic equipment.
• Access to Intertek’s global wellness initiatives, including virtual fitness classes and nutrition webinars.

Work Environment & Culture – What It’s Like to Be Part of Intertek

Intertek’s culture is built on three pillars: Innovation, Integrity, and Inclusion. Our remote teams stay connected through regular video huddles, collaborative platforms, and annual in‑person retreats that foster camaraderie across regions. We celebrate diversity, encourage open dialogue, and champion a safe, drug‑free workplace. Every employee is empowered to raise ideas, challenge the status quo, and contribute to our mission of creating a more secure world.

We also prioritize sustainability. Our corporate responsibility program supports community outreach, environmental stewardship projects, and volunteer days, giving you avenues to make a positive impact beyond the office.

How to Apply – Take the Next Step in Your Career

If you are ready to join a world‑leading quality assurance organization and lead the charge on global food ingredient compliance, we want to hear from you. Please submit your resume, a concise cover letter detailing your most relevant achievements, and any supporting documentation (e.g., publication list, certifications) through the link below.

Apply now and become the regulatory champion our clients trust.

Apply Now

Are You the One We’re Looking For?

Intertek values talent, passion, and a relentless pursuit of excellence. If you believe you have the expertise, drive, and collaborative spirit to thrive in this role, submit your application without delay. We are excited to explore how your unique background can help us continue to set the gold standard in food safety and regulatory excellence.

Apply Now