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Senior Scientific Consultant, Toxicology - 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 Senior Scientific Consultant, Toxicology to join our Assuris team.

This is a fantastic opportunity to grow a versatile career in toxicology.

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 we are looking for?

As a Senior Scientific Consultant, Toxicology at Intertek, you will lead and guide our clients on matters related to regulatory toxicology and compliance to global regulations and expectations for pharmaceuticals.

This role requires a special individual with a deep understanding of, and appreciation for, toxicological risk assessments pertaining to drugs, biologics, and medical devices.

As a subject matter expert, you will have demonstrated expertise in the practices of sound scientific judgment and clear and transparent argumentation to support toxicological risk assessments in report formats that are regulatory-ready.

You will work closely with internal teams and clients, analyzing complex data, preparing professional reports, and managing projects to ensure compliance with global regulatory expectations.

The Senior Scientific Consultant will utilize their knowledge in toxicology and regulatory science to address challenges related to pharmaceuticals, biologics, and medical devices.

This position also provides opportunities to promote and expand Intertek's toxicology consulting services through business development activities and industry engagement.

What you'll do :

Perform toxicological risk assessments, including health-based exposure limits, occupational toxicology evaluations, and qualitative assessments for pharmaceuticals, biologics, and medical devices.

Develop clear justifications and substantiated arguments to support positions taken and conclusions reached in professional regulatory reports.

Provide regulatory toxicology guidance to clients to ensure compliance with global pharmaceutical standards.

Analyze scientific issues and provide sound, rational solutions supported by evidence-based research.

Be responsible for work on and guidance of projects, which typically have major complexities and multiple dimensions / facets, identification of "outside of the box" solutions when needed, and synthesis of findings into clear, well-written reports that discuss the implications of the findings

Manage client relationships and serve as a primary point of contact for project discussions, proposals, and deliverables.

Be an effective supervisor and team leader, responsible for a group or an area of expertise, who makes effective decisions about work to be done and work standards, and who helps plan and supports the growth and development of the business.

Collaborate with internal teams, including senior scientists and regulatory experts, to deliver high-quality consulting services.

Promote toxicology consulting services by identifying business development opportunities and participating in client meetings and industry events.

Prepare cost estimates, proposals, and project timelines to meet client expectations and deadlines.

Provide mentorship and support to junior staff, contributing to their professional development.

Ensure compliance with Intertek's Health, Safety, and Environmental Policies and Procedures, Quality Management System, Compliance and Ethics Policies, Vision, Mission, and Strategy.

Minimum Requirements & Qualifications :

PhD in Toxicology (preferred) or related field, or MSc with extensive relevant experience.

10 years of pharmaceutical industry experience with a primary focus on toxicology, and more specifically toxicological risk assessments

Subject matter expertise in toxicological risk assessments, health-based exposure limits, occupational toxicology, and regulatory compliance for pharmaceuticals.

Demonstrated ability to manage complex scientific projects and deliver high-quality reports.

Strong business acumen with experience in identifying project opportunities and preparing proposals.

Excellent written and verbal communication skills, with the ability to present persuasive and clear arguments.

Proven experience managing client relationships and delivering exceptional customer service.

Ability to work independently and as part of a team in a fast-paced, multi-tasking environment.

Proficiency in project management, including timeline and budget tracking.

Willingness to travel as needed for client meetings and industry events.

Salary & Benefits Information

This is a full-time permanent position.

In addition to competitive compensation packages, when working with Intertek you can expect benefits including medical, dental, vision, life, disability, 401(k) with company match, generous vacation / sick time (PTO), tuition reimbursement and more.

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 hr.eeo@intertek.com or call 1-877-694-8543 (option #5) to speak with a member of the HR Department.

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CA-DRIntertek 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.