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8 часов назад

Regulatory Affairs - Industrial Placement

Формат работы
hybrid
Тип работы
fulltime
Грейд
trainee
Английский
b2
Страна
UK
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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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

hirify.global 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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