Our client is one of the leading global service providers in offering regulatory registration, clinical development and product development support to clients. Their team of scientific and regulatory experts and extensive network of partners ensures that all the different regulatory requirements are right from the project outset to support their client’s global business. People are at the heart of their family-owned business and their values guide the way to their success. Team spirit and mutual support are very important to them. Their culture is characterised by strong international co-operation, can-do attitude, focus on quality and a growth mindset.
Their strength is to be where it matters - think globally, act locally!
Preparation of regulatory strategy for biocide dossiers and their submission in accordance with the BPR (national, EU, Article 89)
Regulatory support to clients
Interaction with authorities
Representation of the company at industry events and conferences / business development"
University degree (Master's or Doctorate) in chemistry, biology, environmental sciences, or equivalent
Minimum of 5 years in the field of regulatory affairs
3 to 5 years of experience in managing EU regulations, particularly the Biocidal Products Regulation (BPR, Regulation (EU) 528/2012) for active substances and biocidal products
IUCLID, R4BP3, and other ECHA submission tools
Proficiency in English is essential.
Practical experience in dealing with various competent evaluating authorities (eCA)
Knowledge of regulations related to chemical products would be an asset