Octapharma develops and manufactures human protein therapies derived from plasma, serving patients with a range of medical conditions. Founded in 1983, the healthcare and biotechnology company operates in more than 100 countries. Its work spans research, production, and patient support, bringing together teams across the business to pursue shared goals.
Regulatory Information Management and Submission Technology Intern
Support validation, data quality, and Power BI reporting as a regulatory information management intern. Help advance digital transformation across Octapharma’s pharmaceutical operations.
Description
- Assist with computerized system validation under GxP requirements
- Prepare, run, and document system tests and validation records
- Help with data migration, verification, and quality checks
- Maintain and analyze regulatory master data
- Create reports and dashboards with tools such as Power BI
- Help develop and update standard operating procedures, work instructions, and system documentation
- Contribute to business process analysis and improvement efforts
- Provide administrative and project support to the Regulatory Information Management and Submission Technology team
- Contribute to digital projects spanning Regulatory Affairs, Information Technology, and Data Management
Requirements
- Be enrolled in a University of Applied Sciences (FH) degree program that includes a compulsory internship
- Preferably study Data Science or Business Analytics, Business Informatics, Software Engineering, Computer Science, Bioinformatics, Health Informatics, or Pharmaceutical or Biotechnology studies with a strong IT focus
- Have a strong interest in digital solutions, data management, and the pharmaceutical industry
- Bring an analytical mindset and excellent problem-solving skills
- Work in a structured and detail-oriented manner
- Have good knowledge of Microsoft Office, especially Excel
- Have basic knowledge of SQL and Power BI
- Experience with software testing or programming is an advantage
- Communicate excellently in English
- German language skills are an asset
- Submit a motivational letter, CV, high school diploma, current transcript from a University of Applied Sciences, and proof of the compulsory internship with the application
Benefits
- Gain a challenging and rewarding internship at an international pharmaceutical company
- Get practical experience in Regulatory Information Management, computerized system validation, and digital transformation projects
- Work with modern regulatory IT systems and data management processes
- Receive guidance from experienced professionals
- Join an international, collaborative workplace
- Use the company restaurant and meal subsidy
- Access training and further education
- Take part in health promotion programs
- Use parking and convenient public transport connections
- Attend company and team events