Regulatory Affairs Intern

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profile Job Location:

Birmingham - UK

profile Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

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 years placement as part of their degree and will start Summer 2026.


Required Experience:

Intern

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionDiscover 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;...
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Key Skills

  • Proofreading
  • Adobe Acrobat
  • FDA Regulations
  • Manufacturing & Controls
  • Biotechnology
  • Clinical Trials
  • Research & Development
  • GLP
  • cGMP
  • Product Development
  • Chemistry
  • Writing Skills

About Company

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Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more

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