Назад
Company hidden
17 часов назад

Senior Analyst, Regulatory Affairs

Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Netherlands
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Senior Analyst, Regulatory Affairs (Food Biosciences): Managing regulatory documentation, product registration files, data repositories, and submission deadlines across multiple markets with an accent on data accuracy, compliance, and document control. Focus on optimizing regulatory systems, supporting digitalization projects, and coordinating cross-functional information flows in a deadline-driven environment.

Location: Leiden, Netherlands; hybrid working opportunities available.

Company

hirify.global develops flavors, fragrances, food ingredients, and health and bioscience solutions, with a focus on sustainable innovation and natural products.

What you will do

  • Support the creation, maintenance, and archiving of Food Biosciences regulatory documentation and product registration files.
  • Maintain regulatory data, databases, document repositories, and electronic filing systems.
  • Coordinate regulatory documentation from cross-functional teams.
  • Track product registrations, renewals, regulatory commitments, and submission deadlines across multiple markets.
  • Ensure data accuracy, consistency, and compliance with internal quality and regulatory standards.
  • Support process improvement, digitalization, and optimization of regulatory systems, templates, procedures, and workflows.

Requirements

  • Bachelor’s degree in Life Sciences, Food Science, Chemistry, Regulatory Affairs, or a related field.
  • 5+ years of experience in Regulatory Affairs, Regulatory Operations, Regulatory Information Management, or a related environment.
  • Strong experience with data management, documentation control, and regulatory record maintenance.
  • Experience managing large volumes of information while ensuring accuracy and compliance.
  • Proficiency with Microsoft Office, SharePoint, and regulatory information management systems.
  • Strong communication, organizational, prioritization, and independent working skills.

Nice to have

  • Experience supporting regulatory digitalization or document management projects.
  • Knowledge of global regulatory registration processes and product lifecycle management.
  • Curiosity, a continuous improvement mindset, and strong problem-solving skills.

Culture & Benefits

  • Opportunity to contribute to a strategic global regulatory project lasting 1–2 years.
  • Exposure to international regulatory processes and cross-functional collaboration.
  • Supportive international work environment with experienced regulatory and scientific professionals.
  • Learning and development opportunities focused on regulatory expertise.
  • Hybrid working opportunities and a focus on work-life balance.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →