München: TEILZEIT - Regulatory Affairs Manager (m/w/d) - Pharma

TN Germany; München; Hybrid; EUR 40.000 - 70.000; Teilzeit

Zusammenfassung

An exciting opportunity awaits you at a biopharmaceutical company in Munich, offering a part-time position as a Regulatory Affairs Manager. In this role, you will oversee the Life Cycle Management of national approvals and collaborate with international teams, ensuring compliance with country-specific regulations. With flexible working hours and a supportive work environment, this position promises not only professional growth but also an attractive remuneration package, including 35 vacation days and various social benefits. Join a diverse team and make a significant impact in the regulatory landscape!

Leistungen

35 vacation days

Flexible working hours

Home office options

Various social benefits

Qualifikationen

• Experience in Drug Regulatory Affairs, including CMC.
• Fluency in German (C1) and English (B2) required.

Aufgaben

• Manage Life Cycle of national approvals and dossier submissions.
• Collaborate with international teams on regulatory requirements.

Kenntnisse

Drug Regulatory Affairs

Communication Skills

Independence

Structured Work Style

Fluency in German

Fluency in English

Ausbildung

Degree in Natural Sciences

Pharmacy Degree

Medicine Degree

Jobbeschreibung

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Job Reference:

29f76b08bdf2

Job Views:

2

Posted:

28.04.2025

Expiry Date:

12.06.2025

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Job Description:

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)

• 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 (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)
• 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:

Tel.: [phone]