• The chance to work in a dynamic stimulating environment with a young and highly motivated team
• RA specialist role - key & central role within the team
• Based in Ghent region

Our client has the vision to make sustainable food production possible.

As a company built on innovation, they constantly work to find ways of helping our customers, dairy farmers, do more with less by providing world-leading milking equipment and solutions.

They core values Passion, People, Professionals and Partnerships connect individuals across entities and geographies. Success is far more than knowledge - it is strongly related to behaviours. All guided by our three behaviours, Setting Direction, Make things happen.

Today, they are approximately ⚠,⚠ passionate professionals operating in more than ⚠ markets around the world.

In order to sustain their growth in EU, they are looking to extend their regulatory affairs team and add a strong team player to drive change & project internally & externally.

As the successful Regulatory Affairs Specialist, you will have the following responsibilities:

• Play a key role in the regulatory information flow and follow-up on registration & compliance projects focussing on Europe
  
  
• Collect needed scientific data, prepare regulatory & risk assessments, registration dossiers, MSDS, and support label instructions for new and existing products within the aftermarket portfolio
  
  
• Follow-up on legislation and guidelines related to BPR, veterinary medicines and hygiene aftermarket in Europe
  
  

In This Role You Will Have Regular Contacts With

• Aftermarket Product Management, Regulatory Affairs & R&D colleagues (internal)
• Regulatory Authorities (external)
• Quality departments (internal)
• Contract labs and consultants (external)

As the successful Regulatory Affairs Specialist - Veterinary, you will have the following requirements:

• A university Degree in Sciences, Agricultural Sciences, Veterinary Sciences, or equivalent
  
  
• A minimum of ⚠-⚠ years' experience in Regulatory Affairs (dossier preparation & submission, compliance, GMP, ISO, manufacturing and quality control of chemicals or pharmaceutical products)£
  
  
• The ability to work independently but also interact in cross functional as well as cross cultural project teams
  
  
• A fluent knowledge of English and Dutch. Basic understanding of other languages (e.g. German, French, Spanish) is an asset
  
  
• Very good communication skills (verbal/written) and computer literate

They offer you a workplace like no other, where state-of-the-art technology goes hand in hand with animal welfare.

• The opportunity to be part of a strong, international organisation
• A competitive salary with an attractive compensation package
• A flexible working schedule including home office
• The chance to work in a dynamic stimulating environment with a young and highly motivated team