Are you an expert in human safety assessments with a passion for navigating complex regulatory landscapes?
For our long-term client, we are seeking a skilled Regulatory Toxicologist to provide strategic guidance and technical expertise in the preparation of registration dossiers for active ingredients and plant protection products. In this role, you will be a key player in ensuring our products meet the rigorous standards of Regulation (EC) No 1107/2009, helping our client achieve their strategic and quality objectives.
The Role: Impact and Responsibilities
As a core member of the regulatory team, you will bridge the gap between complex data and market authorization. Your key tasks will include:
Strategic Evaluation: Conduct Data Gap Analyses, Risk Assessments, and Exposure Estimates to ensure client data meets strict regulatory requirements.
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Program Development: Design experimental strategies and programs that align with European, international, and national data standards.
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Data Synthesis: Summarize and judge experimental work for quality and regulatory focus to support successful authorizations.
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Human Safety Assessment: Prepare comprehensive risk assessments and collaborate with project managers and residue experts to evaluate the overall safety of agrochemical products.
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Project Management: Communicate with third-party consultants and CROs to monitor and manage experimental studies effectively.
Your Profile: Expertise and Vision
We are looking for a candidate who combines deep technical knowledge with a proactive, problem-solving mindset.
Education & Experience:
Advanced Degree: Master’s, Ph.D. in Biology, or Pharm.D. with a specialization in human toxicity.
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Proven Track Record: 2-3 years of professional experience as a Regulatory Toxicologist.
Technical Mastery:
Regulatory Focus: Deep understanding of Plant Protection Products (PPP) or Biocides regulations.
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The “Industry Pivot”: We also welcome strong profiles from the broader Chemicals sector who possess a solid basis in QSAR modeling and study monitoring and feel confident transitioning into the Agrochemical regulatory framework.
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Methodology: Proficiency in in vitro & in vivo study monitoring and utilizing modeling tools for risk assessment.
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Bonus Skills: Experience with IUCLID, Endocrine Disruptor (ED) assessments, or AOP models.
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Communication: Fluency in English; other European languages are an asset.
Personal Attributes:
The ability to work autonomously while maintaining a strong team spirit.
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Analytical excellence and the creativity to solve complex regulatory hurdles.
Why Join Our Client?
You will work in a dynamic, high-stakes environment where your scientific judgment directly impacts business success and environmental safety. They value initiative, information-seeking, and an enthusiastic approach to collaborative work.
Ready your expertise to the future of agrochemicals?
How : Please submit your CV detailing your experience within the toxicology field.
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