Regulatory Watch Consultant
il y a 2 semaines
Amarylys is a Life Science Advisors company specializing in Regulatory and Pharmaceutical Affairs dedicated to the Healthcare Industries. They handle complex projects covering all health products, particularly medicines and medical devices. Their approach is structured around the ISO 9001 standard, ensuring a high level of quality and customer satisfaction.
Why choose Amarylys?
- Be part of a dynamic and caring team where mutual aid and knowledge sharing are essential.
- Contribute to diverse and innovative projects in the healthcare sector, nationally and internationally.
- Develop your skills and expertise with personalized management and continuous training.
- Enjoy a flexible work environment with modern conditions and telecommuting options.
- Benefit from a quality-centric approach built around the ISO 9001 standard.
- Build a promising career in regulatory and pharmaceutical affairs.
Amarylys is looking for a Regulatory Watch Consultant with a passion for the pharmaceutical and regulatory field. The Consultant will be responsible for daily monitoring of regulatory news on medicines, medical devices, biocides, dietary supplements, and cosmetics at French and European levels. Other responsibilities include providing personalized monitoring for Amarylys clients, writing and publishing various articles and collaborating with partners and clients.
Key Responsibilities:- Monitor and analyze regulatory news and updates on medicines, medical devices, biocides, dietary supplements, and cosmetics.
- Provide personalized monitoring services for Amarylys clients, including regular updates and insights.
- Write and publish articles on regulatory topics, including industry trends and best practices.
- Collaborate with partners and clients to provide expert advice and guidance on regulatory matters.
- Minimum Bachelor's degree in Media, Communication, or Journalism with a scientific background or equivalent experience.
- At least 3 years of professional experience in writing, journalism, and content management.
- Excellent writing skills and a keen interest in the pharmaceutical and regulatory field.
- Proficiency in visual creation tools and WordPress, as well as the Microsoft Office Suite and fluent English.
- Analytical and synthetic mindset with attention to detail, efficiency, and methodical approach.
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