München: TEILZEIT – 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 20%-40% homeoffice) we are searching for a:

Regulatory Affairs Manager (m/w/d)
in part-time (20 hours per week)

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 (ideally including CMC, Module 2.3, and Module 3).
• 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 (C1) and English (B2)

What is offered to you:

• Flexible working hours (flexible working time models, home office).
• Attractive remuneration, 35 vacation days, and various social benefits.
• An exciting position in a positive and diverse work environment

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