Supporting the team with administrative and data management activities
Assisting with the preparation of documentation for national product registrations
Data entry and maintenance in IUCLID for regulatory submissions under the EU Biocidal Products Regulation (BPR)
Gathering and structuring regulatory data, including: Safety Data Sheets (SDS), Product composition overviews, Supporting technical documentation, Label generation and document formatting
Supporting organization and clean-up of digital files and folder structures
Assisting the Regulatory Affairs team with general administrative tasks related to product approvals
Requirements
Is currently enrolled in a Bachelor’s or Master’s program (e.g., chemistry, environmental science, engineering, pharmacy, regulatory science, or similar)
Works structured and detail-oriented
Has strong data-handling skills
Is comfortable working with Excel and digital document systems
Has good written and spoken English
Can work approximately 15 hours per week
Experience with regulatory systems, chemical documentation, or databases is an advantage but not required.
Benefits
Insight into international chemical regulatory processes
A flexible student position (~15 hours/week) that can be adapted to your study schedule
The opportunity to work closely with experienced Regulatory Affairs specialists