Apply Now
Apply Now

Vacature

Junior Regulatory Affairs Specialist - Medicines

Are you a life sciences graduate looking to step into Regulatory Affairs? As a Junior Regulatory Affairs Specialist – medicines at Interchemie, you learn how products are registered, maintained and kept compliant throughout their entire regulatory lifecycle.

You will work in an international, English-speaking environment, supporting veterinary medicinal products that are marketed worldwide. This junior role is designed to help you grow into full responsibility for regulatory dossiers, from initial registration to ongoing maintenance, guided by experienced Regulatory Affairs colleagues.

Gegevens

Departament

Research and Development

Salaris

€3500 -

€6000

Locatie

Waalre

Uren

40 -

40u

Solliciteren

Wat ga je doen?

Je nieuwe uitdaging

As our Regulatory Affairs Specialist - Medicines, you make sure that Interchemie’s veterinary medicines can legally and safely be placed on the market. In practice, this means translating scientific product information into complete and compliant regulatory dossiers that meet the requirements of different countries.

 

You work on registrations, renewals and variations. You prepare and maintain regulatory files, coordinate documentation with several departments, handle questions from agents and authorities, and make sure that product information, labels and packaging are aligned with what is registered. Through this work, you follow products throughout their regulatory lifecycle, from initial registration to ongoing maintenance.

You operate in a hands-on, on-site role in Waalre, with responsibility for your own set of countries and dossiers. The role combines regulatory content with practical follow-up, such as handling samples and supporting documentation flows that other teams depend on. Accuracy, ownership and structure are essential, as your work directly affects whether products can be marketed.

This role offers room to grow beyond execution. You are encouraged to think along, ask critical questions and contribute ideas on how registrations, documentation and compliance can be improved. Over time, you gain insight into the full regulatory lifecycle and gradually take on more responsibility.

Impact

Belangrijkste verantwoordelijkheden

  • Take ownership of regulatory dossiers from A-Z for veterinary medicines, including registrations, renewals and variations for a defined group of countries.
  • Prepare, maintain and update regulatory documentation, translating scientific product information into complete and compliant registration files.
  • Work closely with QA and QC and other departments to align documentation, support compliance activities and help determine the right regulatory approach per product or market.
  • Act as a regulatory point of contact for internal teams and external agents, handling questions related to registrations and ongoing dossiers.
  • Support the practical regulatory process on-site, including handling samples and ensuring documentation flows smoothly between teams.

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 junior entry-level position in Regulatory Affairs, offering a clear opportunity to step into the RA field and build a solid foundation within medicines (GMP).
  • A steep learning curve, where you are trained on the job and learn from experienced Regulatory Affairs colleagues who work daily with international regulations and complex dossiers.
  • Exposure to the full regulatory lifecycle of products, from registrations and variations to ongoing maintenance across different countries and markets.
  • A role working closely with QA, QC and other departments, allowing you to quickly understand how Regulatory Affairs fits into the wider organisation.
  • A professional, international working environment with competitive employment conditions, aligned with a junior position and with room to grow as your knowledge and responsibilities incease.

Wat vragen we

  • A Master’s degree in Chemistry, Life Sciences, Biomedical Sciences, Pharmacology, Animal Science or a related scientific field.
  • A clear interest in Regulatory Affairs and the motivation to develop yourself within this field.
  • The ability to work accurately and structured, with attention to detail and an understanding of the importance of compliance.
  • A proactive and learning-oriented mindset: you ask questions, take responsibility for your work and are open to feedback.
  • Good written and spoken English, as English is the working language within the organisation.
  • Availability to work on-site in Waalre, as the role requires close collaboration with other teams and hands-on regulatory activities.
Neem contact op
Lynn van Wonderen
Recruiter
Solliciteren
Heb je interesse? Stuur je CV, dan kom ik zo snel mogelijk bij je terug. Ik kijk ernaar uit om je te leren kennen!

Klaar voor de volgende stap?

Geef vorm aan Dierenwelzijn

Laat je cv achter voor de functie Junior Regulatory Affairs Specialist - Medicines, de koffie staat klaar.

Solliciteren
Ben je klaar voor de volgende stap in je carrière?

Solliciteer nu!

01
Solliciteer
02
Maak kennis
03
Gefeliciteerd!

Upload je CV

Upload eventueel je Motivatie