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Senior Regulatory Affairs Consultant

2 months ago

Boca Raton, United States Intertek Group Full time
Job Description

Regulatory Affairs Consultant - US, Remote

Intertek, a leading provider of quality and safety solutions to many of the world's top-recognized brands and companies, is actively seeking a Regulatory Affairs Consultant to join our Assuris team. This is a fantastic opportunity to grow a versatile career in Regulatory Affairs.

Intertek Assuris is an unparalleled team of industry-leading experts providing science-based assurance in quality, safety, and sustainability. Our global network of scientists, engineers, and regulatory specialists provides support to navigate complex scientific, regulatory, environmental, health, safety, and quality challenges throughout the value chain. Through our regulatory, scientific and industry insights, we empower companies with solutions designed to enable market access, assess and mitigate risk, preserve and promote human health, and protect the environment.

What are we looking for?

The Regulatory Affairs Consultant is responsible for managing regulatory strategies, supporting scientific studies, and maintaining business relationships. This position will travel at least 20% of the time.

What you'll do:
• Oversee the development and execution of regulatory strategies in various jurisdictions.
• Prepare, review, and submit regulatory notifications ensuring accuracy and completeness.
• Communicate with government agencies and senior staff regarding regulatory updates and amendments.
• Write detailed project proposals, manage budgets, and ensure high-quality delivery.
• Create and present marketing and promotional materials to potential clients.
• Maintain regulatory tracking and project management databases.
• Provide regular updates and reports to clients and internal teams.
• Build and nurture a network within the scientific and regulatory communities.
• Identify market trends and business opportunities to drive growth.
• Participate in and contribute to scientific conferences and industry publications.

This position outline is a general guideline and does not represent all-encompassing details. The position assumes that the incumbent has both the mental and physical requirements to carry out the above-defined duties.

Minimum Requirements & Qualifications:
• Degree in science (e.g., environmental science, toxicology, biology, pharmacology, biochemistry).
• 5+ years of experience in regulatory affairs or related field.
• Strong written and verbal communication skills.
• Proven ability to manage projects and lead teams.
• Experience in developing regulatory strategies and preparing regulatory notifications.
• Valid passport required.
• This is a remote position; however, applicants must reside in and be able to legally work in the United States.

Preferred Requirements & Qualifications:
• Degree in an area of toxicology or related field, , e.g., molecular toxicology, physiology, metabolism, pharmacology, anatomy, chemistry, regulatory knowledge, etc.
• Additional certifications in regulatory affairs.
• Experience in business development and client relationship management.
• Participation in industry conferences and publications.

Intertek: Total Quality. Assured.

Intertek is a world leader in the Quality Assurance market, with a proven, high-quality business model and a global network of customer-focused operations and highly engaged subject matter experts. With passion, pace, and precision we work to exceed our customers' expectations, while engaging with our employees to be 10X in their performance and professional growth.

Intertek is a drug-free workplace. As a condition of employment, certain positions may be required to pass a pre-employment drug test based on the type of work that will be performed.

We Value Diversity

Intertek's network of phenomenal people are our greatest assets, and the diversity they bring fuels our success. Intertek is an Equal Employment Opportunity Employer that values inclusion and diversity. We take affirmative action to ensure all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other legally protected characteristics.

For individuals with disabilities who would like to request accommodation, or who need assistance applying, please email [redacted] or call [redacted] (option #5) to speak with a member of the HR Department.

*Intertek does not accept unsolicited approaches from agencies and will not pay a fee for any placement resulting from the receipt of an unsolicited resume.

About Us

Intertek is a leading Total Quality Assurance provider to industries worldwide. Our network of more than 1,000 laboratories and offices in more than 100 countries, delivers innovative and bespoke Assurance, Testing, Inspection and Certification (ATIC) solutions for our customers' operations and supply chains. Working at Intertek means joining a global network of state-of-the-art facilities and passionate people who deliver superior customer service with a purpose of bringing quality, safety, and sustainability to life.

About the Team

Intertek's Health, Environmental & Regulatory Services (HERS) business line is renowned for its high-quality solutions delivered through its global network of world-class scientific, engineering, toxicological and regulatory experts. Additionally, HERS provides regulatory compliance support, as well as industry-agnostic solutions pertaining to sustainability, quality, and safety, empowering companies to mitigate risks and make informed decisions relating to their products and processes.