Discover Impactful Work:
Join a dynamic RA team handling PMS, vigilance, product development, EU IVDR, and global registrations. Daily variety for growth.
A Day in the Life:
- Supporting regulatory affairs and cross-functional teams; providing basic regulatory advice.
- Assist with the regulatory compliance activities and processes.
- Populate and maintain regulatory databases or systems.
- Assist with various internal and external document review/check activities and sign off.
- Assist with compiling materials required for submissions, license renewals and annual registrations.
- Input into parts of regulatory dossiers aligned with local requirements.
Keys To Success:
- Willingness to learn and grow the regulatory expertise.
- Understanding of the PDX business and interaction between the various departments.
- Basic understanding of products, manufacturing processes and their applications.
- Understanding of the various regulations and regulatory systems.
- Demonstrating strong organisation skills and ability to work to deadlines.
- Support the regulatory team to maintain and/or achieve compliance.
Education:
- Studying a BSc in Regulatory Affairs, Quality or Life Sciences degree
Experience:
- Experience in biology, healthcare, or related fields desired.
- Experience in regulatory affairs/quality assurance preferably in IVD industry desired.
Knowledge, Skills, Abilities:
- Good communicator, fast learner.
- Proven track record of working to deadlines.
- Ability to manage time efficiently.
- Works well in a team environment and on own initiative.
- Capable of handling and delivering basic company/product-related information to regulatory bodies, or internal/external collaborators.
This is an internship for students looking for a year's placement as part of their degree and will start Summer 2026.
