Key Responsibilities
- Handel and process all administrative documents and requirements such as: Statements, Power of Attorney, Free sale certificates and Certificate of Pharmaceutical products.
- Support the team members in activities related to their coordination of Regulatory Life Cycle Management activities within part of our healthcare brands.
- Ensure that the Regulatory Information Management system (Veeva RIMs) is maintained and updated for all activities under role responsibility.
- Keep all required internal trackers up to date.
- Complete analysis and tasks on-time and keep manager/daily - coach informed of progress.
Job Qualifications
YOUR PROFILE
- You successfully finished an apprenticeship as MTA/PTA or dual studies (Duales Studium)/Bachelor in Life-Sciences.
- You’re proficient in German and English.
- Excellent attention to detail, good communication and good presentation skills.
- You can handle competing priorities effectively with good planning and organizational skills.
- Strong initiative and follow-through with accountability for work quality.
- You work independently in a matrix environment to build superior relationships with stakeholders.
- You are results oriented, self-motivating, open to change and think out the box.
- Knowledge of Microsoft Power Automate and/or Power BI is a plus.