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Regulatory Affairs Specialist

Tired of working on just one small part of the regulatory process?

At Interchemie, it’s different. As a Regulatory Affairs Specialist, you are involved in the entire lifecycle of a product, from preparing and submitting registrations to maintaining dossiers and managing variations across international markets.

Unlike many Regulatory Affairs positions in the Netherlands, this role does not require Dutch. The entire RA team works in English.

Gegevens

Departament

Research and Development

Salaris

€3500 -

€6000

Locatie

Waalre

Uren

40 -

40u

Solliciteren

Wat ga je doen?

Je nieuwe uitdaging

As a Regulatory Affairs Specialist, you are responsible for managing regulatory dossiers from A to Z. From preparing and submitting new registrations to maintaining variations and renewals, you oversee the regulatory process throughout the entire lifecycle of a product.

Your work is closely connected to the rest of the organization. You collaborate daily with colleagues from QA, QC, logistics and sales to make sure products can be registered, released and shipped without delays. Regulatory Affairs sits at the center of this process: if the documentation is not correct or complete, products cannot move forward.

At the moment the team is working on several large projects, including the transfer of registrations to a new manufacturing site and the integration of dossiers from newly acquired companies. This means you will step into an environment where regulatory work is not only operational, but also requires ownership, problem solving and collaboration across teams.

Through experience you already understand that working in a regulated environment means that accuracy, documentation and consistency matter in practice. Small details can have large consequences for registrations, so attention to detail and a structured way of working are essential.

At the same time, the role offers variety and international exposure. You will work with dossiers for multiple regions and interact with agents and authorities across different markets, while gaining a complete view of the regulatory lifecycle of veterinary medicines.

Impact

Belangrijkste verantwoordelijkheden

  • Prepare, compile and submit regulatory dossiers for new product registrations across international markets
  • Manage the full lifecycle of regulatory dossiers, including variations, renewals and updates
  • Take ownership of a portfolio of countries and ensure registrations remain compliant and up to date
  • Maintain and organize regulatory documentation according to country-specific regulatory requirements
  • Communicate with regulatory authorities, agents and partners regarding submissions, questions and approvals
  • Monitor regulatory developments and ensure product documentation remains aligned with regulatory requirements
  • Collaborate closely with QA, QC, logistics and sales to ensure products can be registered, released and supplied to the market
  • Support the transfer and maintenance of registrations when manufacturing sites or product documentation change
  • Contribute to improving regulatory processes, documentation and internal workflows

Over de werkgever

Over Interchemie

Interchemie is een internationaal opererende familieonderneming die diergeneesmiddelen, nutritionals en desinfectiemiddelen ontwikkelt en produceert. Vanuit het hoofdkantoor in Waalre en productielocaties in Nederland, Estland en Litouwen bedient Interchemie klanten in meer dan 100 landen via zorgvuldig geselecteerde distributeurs. De afgelopen jaren laat Interchemie een structurele groei in dubbele cijfers zien.
Recent hebben Interchemie en Kepro de handen ineengeslagen. Kepro is eveneens actief in diergezondheid en heeft een sterke internationale positie, met name in Afrika en het Midden- Oosten. Door deze overname zijn kennis, portfolio en commerciële slagkracht verder versterkt en ontstaan nieuwe groeikansen in bestaande en nieuwe markten.
De gezamenlijke ambitie is helder: verdere uitbouw van het marktaandeel in strategische regio’s, met Afrika als belangrijk speerpunt. Betrouwbaarheid, kwaliteit en langdurige samenwerkingen met distributeurs staan daarbij centraal.

Wat krijg je

  • A Regulatory Affairs role where you are involved in the full product lifecycle instead of just one part of the process
  • Responsibility for your own portfolio of countries and regulatory dossiers
  • An international working environment with registrations across many different markets
  • A close collaboration with QA, QC, logistics and sales within a growing organization
  • The opportunity to develop your expertise in Regulatory Affairs while working on a broad range of products and markets
  • A competitive salary and good secondary employment conditions
  • A full-time position based in Waalre

Wat vragen we

  • A Master’s degree in Chemistry, Biomedical Sciences, Life Sciences or a related field
  • Experience working in Regulatory Affairs or a regulated pharmaceutical or life sciences environment
  • Accuracy and a structured way of working with regulatory documentation
  • The ability to manage multiple dossiers and regulatory requirements simultaneously
  • Strong communication skills and the ability to collaborate with colleagues and external partners
  • Fluency in English (Dutch is not required)
  • Availability to work on-site in Waalre
Neem contact op
Lynn van Wonderen
Recruiter
Solliciteren
Are you the Regulatory Affairs Specialist we are looking for? Click the button to apply. - You will receive a response within a few working days. - I will first call you for a short introduction. - After that we will schedule a meeting at our office with Heetika (RA Manager) Do you have questions or would you like to discuss the role first? Call or message me: Lynn van Wonderen at 06-58821266 or send me an email to lynn@jobin.nu.

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