An exciting opportunity has arisen to work for a biopharmaceutical company, with a successful product portfolio.
For the office located in Munich (in combination with 60% homeoffice) we are searching for a:
Senior Regulatory Affairs Manager (m/w/d)
Aufgaben
- You will be responsible for the Life Cycle Management (including CMC) of national approvals and the submission of dossiers in new countries.
- You cooperate with our international counterparts and track the implementation of country-specific regulatory requirements.
- You will oversee development projects in collaboration with interdisciplinary teams.
- You will take on tasks related to maintaining our regulatory databases and the creation and review of SOPs.
- Furthermore, you will handle organizational tasks within the Regulatory Affairs department.
Qualifikation
- You have a degree in natural sciences, Pharmacy or Medicine
- You have substantial experience in Drug Regulatory Affairs (including CMC, Module 2.3, and Module 3) and can independently develop regulatory strategies
- You possess a high level of decisiveness and value working independently
- You have a structured work style and very good communication skills
- You are fluent in both German and English.
Benefits
- A diverse work environment
- Flexible working hours (flexible working time models, 37.5 hours/week, home office)
- Attractive remuneration, 30 vacation days, and various social benefits
Do you want to know more about this position?
Please send your complete application to:
Silvio Di Meglio
Tel.: 089-80913072-1
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Zuletzt aktualisiert am 19.04.2024