Regulatory Affairs Specialist (m/f/d)

GULP – experts united; Hamburg; Vor Ort; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

A global leader in skin care and cosmetics seeks a Regulatory Affairs Specialist in Hamburg. The role involves planning product approvals, managing compliance, and coordinating with stakeholders. Ideal candidates will possess a scientific degree and relevant experience, with strong project management capabilities and excellent English skills.

Leistungen

Attractive salary and long-term job security

Up to 30 days vacation per year

Company pension scheme contributions

Social benefits including bonuses

Travel expense reimbursement

Open-ended employment contract

Opportunities for permanent placement

Training and language courses

Qualifikationen

• Degree in a scientific or technical field.
• Experience in regulated product approval.
• Knowledge of international regulations and drug approval is a plus.

Aufgaben

• Global product approval planning and coordination.
• Development and implementation of approval strategies.
• Regulatory compliance management.

Kenntnisse

Project Management

Attention to Detail

Organization Skills

Excellent English

Ausbildung

Scientific or Technical Degree

Tools

SAP

Digital Tools

Jobbeschreibung

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Regulatory Affairs Specialist (m/f/d), Hamburg

Location: Hamburg, Germany

Job Category: Other

EU work permit required: Yes

Job Reference: ca18d2aae0d7

Job Views: 3

Posted: 21.06.2025

Expiry Date: 05.08.2025

Job Description:

Our client, a global leader in skin care, cosmetics, and wound care, is seeking a Regulatory Affairs Specialist (m/f/d) in Hamburg. Join us to actively shape your future and benefit from our extensive network!

We offer:

• Attractive salary and long-term job security
• Up to 30 days vacation per year
• Company pension scheme contributions after probation
• Social benefits including bonuses
• Travel expense reimbursement
• Open-ended employment contract
• Opportunities for permanent placement
• Training and language courses
• Global product approval planning and coordination
• Development and implementation of approval strategies
• Regulatory compliance management
• Authority and stakeholder coordination
• Management of digitalization projects

Your profile:

• Scientific or technical degree
• Experience in regulated product approval
• Knowledge of drug approval is a plus
• Understanding of international regulations
• Strong project management skills
• Excellent English skills
• SAP and digital tools knowledge advantageous
• Attention to detail and organization skills