Regulatory Ecotoxicologist

at  Charles River Laboratories

5231 Den Bosch, Noord-Brabant, Netherlands -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate23 Jan, 2025Not Specified24 Oct, 2024N/ABiocides,Assessment,Industrial Chemicals,Pharmaceuticals,Risk Assessment,Project Coordination,Compilation,AgrochemicalsNoNo
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Description:

Al meer dan 75 jaar werken de medewerkers van Charles River samen om te helpen bij het ontdekken, ontwikkelen en veilig maken van nieuwe geneesmiddelen. Wanneer u bij onze familie komt, heeft u een belangrijke impact op de gezondheid en het welzijn van mensen over de hele wereld. Of uw achtergrond in levenswetenschappen, financiën, IT, verkoop of een ander gebied is, uw vaardigheden spelen een belangrijke rol in het werk dat we uitvoeren. In ruil hiervoor helpen wij u een carrière op te bouwen waar u over gepassioneerd kunt voelen.
Are you looking for a varied job in an international working team? Bringing your knowledge and expertise together with other experts to come to a tailored support to our client needs?
Our Regulatory Affairs department, one of a kind within Charles River is organized in two sections:
Regulatory Environmental Toxicology and Chemistry, and Regulatory Toxicology.
For the first section we are looking for a new colleague

YOUR ACTIVITIES INCLUDE, DEPENDING ON YOUR INTERESTS, KNOWLEDGE AND EXPERIENCE:

  • Evaluation and assessment of all aspects of ecotoxicology data;
  • Compilation of ecotoxicology sections for primarily agrochemical dossiers (both active substances and plant protection products) and, depending on the candidate’s knowledge and experience, eventually other legislative frameworks (industrial chemicals, biocides, pharmaceuticals).
  • Performance of environmental risk assessment for agrochemicals and eventually industrial chemicals, biocides and/or pharmaceuticals – both lower and higher tiers;
  • Advising clients on regulatory aspects as well as on generation of ecotoxicological data and evaluation and environmental risk assessment;
  • When necessary and/or interested, project coordination;
  • Working closely together with your own regulatory team members, our study directors, sales and client services team, as well as staying in contact with clients and authorities;
  • Presenting at (inter)national conferences and participating in internal and/or external working groups.

Responsibilities:

Please refer the Job description for details


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

5231 Den Bosch, Netherlands