Munich: Senior Regulatory Affairs Manager (m/w/d) – Pharma –

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)

The tasks:

• 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

The desired profile:

• 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.

What is offered to you:

• 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
dimeglio@triga-consulting.de