Regulatory Affairs Officer Bpr for The Animal Health Division
il y a 2 semaines
At CID LINES, an Ecolab Company we believe that hygiene leads to better health, which in turn is the key to greater profitability and sustainability. In the agricultural sector and food industry, health and safety generate better operations in compliance with all regulations. Overall, the end consumer will always reap the benefits of a healthy food chain, which promotes overall well-being. Is your ideal job a job where you will be part of an international yet family-oriented company, where you will be given responsibility and where you will be able to learn a lot? Then this is the job you are looking for
**What you will do**:
In this position, you will join our Regulatory affairs team and report to the Regulatory affairs manager:
- You participate to the set-up of the regulatory strategy for the European authorization of the biocidal products of the Global Animal Health division.
- You partner with stakeholders to run competitor analysis and positioning strategies for biocidal products.
- You are responsible for preparing, submitting and following up the European registration dossiers for biocides (Biocidal Product Regulation BPR). You defend the authorization process and address evaluation questions from EU and member state authorities with the internal registration project team and possibly with external partners
- You develop and prepare the risk assessments for human health, environment, animal health, dietary risk mainly for biocidal product for both registration purposes and R&D support. You have a critical eye on the risk assessment and you initiate discussion with relevant stakeholders within the organization when relevant.
- You maintain close contacts with authorities, external and internal stakeholders such as distributors, sales department, marketing, R&D, microbio ad phys-chem lab
- You provide regulatory surveillance (i.e. intelligence) and business impact assessment of emerging regulations, actively engaging and communicating to stakeholders within the organization (e.g., R&D, Marketing). In addition, you manage our database and documentation.
**What we are looking for**:
Scientific background in environmental sciences (toxicology, ecotoxicology, chemistry, pharmacy, biology...): bachelor or master degree
Minimum of 2 years of experience in risk assessments and/or BPR
Ability to prioritize tasks effectively and excellent time management skills
Proven project management, communication and problem-solving skills in a regulated environment
As a fluent communicator the English language is indispensable to you, other languages adorn you (French, Italian, Spanish, German )
You are self-motivated, able to work autonomously
You are accurate, you like to go into details, to spend time searching in guidance, to work on excel, you’re perseverant, rigorous and you do not lose to overall view, you’re able to think out of the box and you know how to prepare synthetic summaries
You are solution-oriented, eager to learn
You are a team player and you have a sense of ethic and responsibility
**What we do offer**:
You will grow in a team with broad scientific and regulatory expertise.
You will receive full training on regulatory and risk assessments.
Work is based in Ieper office but can be remote depending on experience.
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