Regulatory Affairs Intern Opportunity at Orifarm | Apply Now
Regulatory affairs intern opportunities in the pharmaceutical industry are becoming highly competitive, especially for students looking to build a career in regulatory operations and life sciences. Orifarm is now hiring Student Assistants for its RA Specialty Rx and OTC team in Denmark. This exciting life sciences job offers hands-on exposure to regulatory data management, ISO IDMP implementation, and pharmaceutical compliance processes while working in a collaborative European healthcare environment. If you are searching for Orifarm jobs or a job in Europe, this opportunity could be the perfect start to your professional journey.
- Job Position: Student Assistant – RA Specialty Rx and OTC
- Job Location: Odense S, Denmark
About the Company
Regulatory affairs intern positions at Orifarm provide students with the opportunity to work in one of Europe’s leading pharmaceutical companies. Orifarm is Europe’s largest parallel importer of pharmaceuticals and Denmark’s largest pharmaceutical supplier, employing more than 2,200 professionals globally.
The company focuses on improving access to affordable and high-quality healthcare products and medicines. Through innovation, digital transformation, and regulatory excellence, Orifarm continues to create better healthcare solutions for people and societies across Europe. Orifarm promotes diversity, inclusion, collaboration, and professional growth, making it an excellent workplace for students seeking a meaningful life sciences job and international exposure.
Regulatory Affairs Intern Description
Regulatory affairs intern roles at Orifarm involve supporting regulatory data operations and maintaining medicinal product information across internal and external systems.
Selected candidates will contribute to the implementation of updated digital standards for medicinal product data, particularly ISO IDMP initiatives. The role also provides exposure to pharmaceutical regulatory processes, data quality management, and operational compliance activities. This life sciences job is ideal for students who want practical experience in the pharmaceutical and healthcare sector.
Qualifications
Regulatory affairs intern applicants should meet the following requirements:
- Currently enrolled in a relevant degree program such as Life Sciences or related fields
- Interest in pharmaceutical industry operations and regulatory processes
- Strong attention to detail and structured working style
- Comfortable working with data and IT systems
- Proactive mindset with strong collaboration skills
- Good written and spoken English communication skills
Students searching for Orifarm jobs with practical learning opportunities in Europe are encouraged to apply.
Key Responsibilities – Regulatory Affairs Intern
Regulatory affairs intern responsibilities at Orifarm include:
- Supporting data collection, maintenance, and quality checks of medicinal product data
- Assisting with updates in Orifarm internal systems and EMA systems
- Contributing to the implementation of new operational processes
- Supporting documentation of regulatory processes and guidelines
- Collaborating with Regulatory Affairs teams to maintain compliance and consistency
- Performing ad hoc administrative and operational tasks
These responsibilities provide valuable exposure to pharmaceutical regulatory operations and digital transformation projects.
Why Join Orifarm?
Regulatory affairs intern opportunities at Orifarm come with several professional and personal benefits. Students will become part of the Student Network (SNO), where more than 70 student assistants connect through social and professional events. The company also offers opportunities for internships, thesis collaborations, and long-term career growth. This makes Orifarm one of the most attractive employers for students seeking a job in Europe within the pharmaceutical and healthcare sector.
