Consultant Regulatory Affairs Biocides

Il y a 2 mois


Mechelen, Belgique ENSUS CONSULTING Temps plein

**Who are we?**

**Ensus Consulting BV is a consulting and services firm operating at the interface between science, government and industry. We provide tailor-made Regulatory Affairs dossier management services to national and international customers covering all aspects of dossiers related to chemicals legislations (BPR, CLP, ED properties, etc.). In order to further expand our small regulatory affairs team, we are seeking one or more highly motivated new colleague(s).**

**Profil**:
**What will you be doing?**

**After an initial period of training on-the-job, you will soon be expected to work independently. You will support companies in their regulatory challenges related to chemical products, incl. biocides. You will coordinate and support regulatory dossiers, both for national and European regime, from A to Z. The latter includes for example setting up challenging efficacy testing scenarios, discussions with laboratories on analytical testing, dossier creation, etc. Furthermore, you will be able to take part to European discussions on drafting the guidance and commenting on existing guidance documents, as well as on existing software for risk calculation (EUSES, Chesar platform, SimpleTreat,...).**

**While we strongly value the capacity to work independently, it is also essential to cooperate with your colleagues, external partners and experts, authorities and our (inter)national customers.**

**Who are we looking for?**

**- **be a recent graduate (Master or PhD level) in a life sciences discipline (chemistry, biology, biosciences, bioengineering,.).**

**- **be eager to develop expertise in the main aspects involved in dossier preparation: analytical chemistry, microbiology, efficacy, (eco)toxicology, exposure assessment, risk assessment, modelling, classification and labelling,...**

**- **preferably have relevant experience in research projects, through internships or industry trainee programmes. While demonstrated experience in executing regulatory projects (BPR, PPPR, CLP,. ) would be beneficial, it is not strictly required.**

**- **preferably have a background and/or experience in toxicology, although this is not strictly required.**

**- **have the following analytical skills: a keen eye for detail, collecting and analysing data with a critical eye, enjoying solving complex problems.**

**- **have excellent writing and organisational skills, good interpersonal skills, responsibility and a critical mind.**

**- **be fluent in written and spoken English, any additional language skills (Dutch, French, German,. ) are of course highly valued.



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