Toxicologist W/M

OverviewWe are one of the world’s leading Contract Research Organizations (CROs), with the commitment, expertise, and flexibility needed to successfully conduct clinical studies. We partner with pharmaceutical, biotechnology, and cosmetic companies, among others, providing innovative and customizable solutions tailored to their needs. Operating in 10 countries across 3 continents, we bring together over 1,000 talented professionals who are dedicated to actively advancing clinical research. Since 2014, we have been part of the ALTEN Group, and we are continuously exploring new opportunities to expand our business worldwide.Who We AreWe are one of the world’s leading Contract Research Organizations (CROs), with the commitment, expertise, and flexibility needed to successfully conduct clinical studies. We partner with pharmaceutical, biotechnology, and cosmetic companies, among others, providing innovative and customizable solutions tailored to their needs. Operating in 10 countries across 3 continents, we bring together over 1,000 talented professionals who are dedicated to actively advancing clinical research. Since 2014, we have been part of the ALTEN Group, and we are continuously exploring new opportunities to expand our business worldwide.Key ResponsibilitiesCoordinate the collection, analysis, and interpretation of toxicological data for raw materials and ingredients (studies, SDS, supplier data, regulatory databases).Contribute to regulatory compliance management of formulations, working closely with R&D, Regulatory Affairs, Quality, and Marketing teams.Oversee the analysis of impurities, traces, or contaminants, and assess their toxicological impact on the safety of the final product.Draft clear and well-documented safety assessment reports, in compliance with cosmetic regulations.Communicate effectively on the progress of safety assessments and monitor priorities related to product safety.Desired ProfileYou hold a scientific degree: PharmD, Master’s (MSc), or PhD in Toxicology.You have at least 2 years of experience in safety assessment of cosmetic products, either in the industry or within a consulting firm.You perform comprehensive toxicological evaluations as part of the Product Information File (PIF – Parts A & B).You ensure regular scientific and regulatory monitoring, particularly regarding controversial substances.You are capable of writing clear, well-argued toxicology reports that comply with regulatory requirements.You collaborate effectively with R&D, regulatory affairs, quality, and marketing teams to ensure product safety and compliance.You are able to manage multiple projects simultaneously while meeting deadlines, budget constraints, and quality standards.Experience in a regulated environment (cosmetics, pharmaceuticals, or chemicals) is a strong asset.You are fluent in English.Joining Aixial Group meansBeing at the forefront of clinical research: You will work on cutting-edge projects where your expertise will make a real impact on the lives of millions of people.Continuously developing your career and skills: Our employees are at the heart of everything we do. At Aixial Group, you will receive mentoring and guidance throughout your journey to support your growth, both professionally and personally.Working in an environment where equality, diversity, and inclusion are central to our commitment: We strive to promote a workplace based on dignity and respect, where individual differences are recognized and valued, and where each employee can thrive. Gender equality is a core focus of Aixial Group’s development strategy.Aixial Group is growing and actively recruiting in the field of clinical research — come join usExplore our career page: https://www.aixialgroup.com/join-us/Learn more on LinkedIn: https://www.linkedin.com/company/aixialgroup/about #J-18808-Ljbffr