ARCHE Consulting, located in Ghent and Leuven, provides regulatory compliance services for manufacturers or importers of chemicals, biocides, cosmetics, plant protection products, fertilizers, and plant bio-stimulants. We guide our clients through the complex regulatory landscape to secure national or EU market access for their products.
With a strong track record of more than 25 years, our team of experts provide timely and cost-effective strategic support in several regulatory areas, including:
- Product registration for market approval
- Data gap analyses
- (Eco)toxicology, exposure modelling & risk assessment
- Test monitoring
- Dossier compilation and submission
- Communication/advocacy with competent authorities
At ARCHE Consulting, we are dedicated to fostering a sustainable environment and a healthy workplace while ensuring market access for chemicals and products. We are well-positioned to support our clients in meeting the goals of the European Green Deal and the Chemical Strategy for Sustainability, which aims to create a toxic-free environment in the EU. We can help you avoid the use of harmful chemicals and boost your innovation for safe and sustainable solutions.
https://www.arche-consulting.be/
Job description
You will be part of an expert team dealing with several chemical legislations (REACH, Biocides, Plant Protection Products etc.). As a Regulatory Human Toxicologist you will be responsible for:
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Monitoring, analysing and summarising toxicological data in view of regulatory submissions in the EU.
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Providing specialist scientific advice and assisting in dossier preparation for several chemical legislations in the EU, including the additional requirements imposed by the EU in different legislations concerning endocrine disruptor (ED) assessment of substances.
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Liaising with regulatory authorities.
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Staying updated on developments and changes in EU toxicology and regulatory requirements.
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Communicating with clients and regulatory authorities if necessary.
Your Profile
Minimum qualifications for this position include:
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Masters degree or PhD in industrial hygiene, toxicology, pharmacology, biology, biomedical sciences or related fields
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Ability to evaluate scientific literature and interpret toxicological data
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A track record of monitoring toxicological studies is considered a plus.
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Acquaintance with the regulatory framework for human health hazard and risk assessments in the EU. Experience with one of the following registration procedures is a plus: Biocidal Products Regulation, Plant Protection Products Regulation, REACH/CLP.
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Expertise related to endocrine-disrupting properties is considered a plus.
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Strong technical and data evaluation skills
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Outstanding oral and written communication skills
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Fluent in English. A good command of Dutch or other European languages is a plus.
What do we offer
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A challenging role in a growing company where you can apply and further develop skills.
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A participative company culture, where you can take initiative, share your ideas and where your opinion counts.
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A nice bunch of colleagues, always ready to help you and in for some fun. You’ll be able to get to know them even better during activities such as our monthly breakfast, weekly sport, yearly teambuilding activities and kids day.
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Flexibility in the organization of your work (e.g. partial working from home), with eye for a healthy work/life balance, as long as the work gets done.
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A competitive salary package, including extralegal benefits (group insurance, bonus system, health insurance) and a flexible reward plan, allowing you to select a number of benefits according to your needs and interests.
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An attractive holiday system (20 + 12 days).
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A professional environment which supports you in your personal development & growth, by means of internal/external trainings, coaching, etc.
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An international dimension in your work.
