Launch Your Regulatory Career in a High-Growth Industry

Step into the world of pharmaceutical cannabis with Curaleaf International. We're looking for a detail-driven Junior Regulatory Affairs Associate ready to make an impact from day one. If you’ve got pharmaceutical experience and a passion for precision, this is your gateway to a dynamic, global career.

At Curaleaf International, we're not just participating in the cannabis industry—we're leading it.

As part of the world’s largest cannabis company, Curaleaf Holding, Inc., we are powered by a strong presence at all stages of the supply chain. Our unique distribution network throughout Europe, Canada and Australasia brings together pioneering research with cutting-edge cultivation, extraction, and production. Amidst a rapid growth trajectory, our emphasis on quality and expertise aims to deliver safe and legal cannabis.

Our Vision: To shape the future of cannabis through our commitment to research and product excellence

Our Mission: To be the world’s leading cannabis company consistently delivering superior products and services and driving the global acceptance of cannabis.

Our Values:

• Lead & Inspire
• Commit to Win
• Driven to Deliver Excellence
• Customer Obsession
• One Curaleaf
  
  

Position:

As an entry-level position, this is an excellent opportunity for a motivated individual to start a career in pharmaceutical regulatory affairs. As a Junior Regulatory Affairs Associate, you will support the Regulatory Affairs team in preparing, compiling, and maintaining essential documentation for our product portfolio in the EU and other international markets. You will play a crucial part in ensuring the accuracy and compliance of our submissions and will contribute directly to our mission of bringing vital medicines to patients. You will be included in various aspects of the regulatory lifecycle, working closely with experienced professionals to achieve key company goals. Duties will include, but not be limited to:

• Adhering to all regulations while compiling and managing documetation
• Maintaining databases and archives
• Information gathering and supporting submissions
• Compiling correspondence and communication from the team
• Liaising company-wide to provide cross-functional support
  
  

Requirements:

Although this could be your first step into Regulatory Affairs, you must have previous experience working for a pharmaceutical company and an awareness of the strict guidelines within the industry. It is essential you:

• Are proficient with office software, particularly Word and Excel
• Have experience of working on research projects involving document compilation, data analysis, and adherence to specific guidelines
• Can write fluently in both Spanish and English
  
  

Although not compulsory, it would be beneficial if you have experience in a quality or compliance related discipline as well as experience of handling controlled substances.

A pre-university higher degree (Grado Superior) in a scientific discipline, ideally related to pharmacy or chemistry, would also provide a good foundation to this role.

Other information:

If this sounds like an ideal role for you, don’t delay in getting your application in! This vacancy may be closed early due to a high level of interest.