Regulatory Affairs Consultant (Remote)

Regulatory Connect; München; Remote; EUR 60.000 - 90.000; Vollzeit

Zusammenfassung

A leading regulatory consultancy is seeking a Senior Regulatory Affairs Consultant in Munich, Germany. In this role, you will provide regulatory expertise for global pharmaceutical projects, ensuring compliance with local regulations. Ideal candidates should have over 5 years of experience in regulatory affairs and a life sciences or pharmacy degree. This position offers flexibility, autonomy, and the opportunity to work with respected experts in the field.

Leistungen

Competitive rates

Flexibility & autonomy

Support from an experienced team

Qualifikationen

• Minimum 5 years’ experience in local regulatory affairs.
• Experience with local submissions and labelling compliance.
• Ability to work in a remote environment.

Aufgaben

• Provide country-level regulatory expertise.
• Support MAAs, national labelling, and health authority interactions.
• Review artwork and manage affiliate SOPs.

Kenntnisse

Regulatory expertise

Attention to detail

Client-facing skills

Delivery-focused mindset

Ausbildung

Life sciences or pharmacy degree

Tools

Veeva Vault

MS Teams

Word

Excel

Jobbeschreibung

Regulatory Connect is seeking experienced Senior Regulatory Affairs Consultants to join our client who has an expanding network of experts across Europe. If you thrive in a dynamic, client-facing environment and want to work on global pharmaceutical projects that truly make a difference, we want to hear from you.

Locations : Germany| Austria

Why Work With this client?

• Global Projects : Partner with some of the world’s leading pharmaceutical companies.
• Flexibility & Autonomy : Remote consulting with full support from an experienced team.
• Meaningful Work : Deliver impactful regulatory solutions that contribute to patient safety and public health.
• Competitive Rates : Reflecting your expertise and value.
• Collaborative Culture : Work with some of the most respected minds in regulatory affairs.

What You'll Do :

You'll provide country-level regulatory expertise, supporting a wide range of responsibilities, from MAAs and national labelling to affiliate SOPs, renewals, artwork review, and health authority interactions. Experience with local submissions, Veeva Vault RIM, and labelling compliance is important.

What they're looking for :

Minimum 5 years’ experience in local regulatory affairs within your country

Life sciences or pharmacy degree

Strong attention to detail and delivery-focused mindset

Comfortable with tools like Veeva Vault, MS Teams, Word, Excel