8 часов назад
Regulatory Affairs - Industrial Placement
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Regulatory Affairs - Industrial Placement (Pharmaceuticals/Healthcare): Supporting regulatory submissions, product documentation, databases, launches, and lifecycle management for medicines and vaccines across the UK and Ireland with an accent on regulatory compliance, product information, and cross-functional collaboration. Focus on preparing submissions, maintaining registration records, reviewing documentation, and presenting recommendations for regulatory projects.
Location: Reading Head Office, United Kingdom; full-time hybrid position with 3 days in the office and 2 days working from home. Start date: 1 July 2027. Duration: 13 months, until 31 July 2028.
Company
is an R&D-driven, AI-powered biopharmaceutical company developing medicines and vaccines to improve patient outcomes.
What you will do
- Develop practical knowledge of regulatory requirements through hands-on experience.
- Support the preparation and tracking of regulatory submissions to UK and Ireland health authorities.
- Review product documentation and maintain regulatory databases, product information, and registration records.
- Assist with new product launches and lifecycle management across a diverse portfolio of medicines and vaccines.
- Collaborate with local and global colleagues across multiple functions to support compliance and business objectives.
- Own assigned projects, present recommendations, and contribute to knowledge sharing and process improvements.
Requirements
- Currently undertaking an undergraduate Life Science degree and returning to university after the placement.
- Curiosity and genuine interest in the pharmaceutical industry and healthcare.
- Patient-focused mindset and motivation to improve patient outcomes.
- Strong communication, collaboration, organisation, and attention to detail.
- Initiative, willingness to learn, and ability to manage multiple priorities accurately.
- Previous pharmaceutical or Regulatory Affairs knowledge is beneficial but not required; full training is provided.
Culture & Benefits
- Inclusive and flexible workplace supporting personal and professional well-being.
- Access to digital tools, innovation, and continuous learning opportunities.
- Mentoring and immersive experience with Regulatory Affairs professionals.
- Opportunities to work on meaningful projects and build an industry network.
- Role is limited to Head Office Regulatory Affairs activities and does not include clinical, laboratory, or manufacturing work.
Hiring process
- Face-to-face assessment days take place in December 2026.
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