Regulatory Affairs Consultant (Remote)

Regulatory Connect; Frankfurt; Remote; EUR 80.000 - 100.000; Vollzeit

Zusammenfassung

A leading regulatory consulting firm in Germany is seeking a Senior Regulatory Affairs Consultant to provide country-level expertise on global pharmaceutical projects. The ideal candidate will have a minimum of 5 years in regulatory affairs and a life sciences or pharmacy degree. This position offers remote flexibility and meaningful work with top pharmaceutical companies, emphasizing autonomy and collaboration.

Leistungen

Flexible work arrangements

Competitive rates

Collaborative culture

Qualifikationen

• Minimum 5 years’ experience in local regulatory affairs.
• Strong attention to detail and delivery-focused mindset.
• Experience with local submissions and labelling compliance.

Aufgaben

• Provide country-level regulatory expertise for various projects.
• Support MAAs and national labelling tasks.
• Interact with health authorities as needed.

Kenntnisse

Regulatory Affairs expertise

Attention to detail

Familiarity with tools like Veeva Vault

Ausbildung

Life sciences or pharmacy degree

Tools

Veeva Vault

MS Teams

Microsoft Word

Microsoft 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