Regulatory Affairs Specialist (m/f/d)

TN Germany; Hamburg; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A global leader in skin care and cosmetics is seeking a Regulatory Affairs Specialist in Hamburg. This role involves driving global product approvals, ensuring compliance with international regulations, and managing digitalization projects. The ideal candidate will have a strong background in regulatory affairs, excellent project management skills, and proficiency in English.

Leistungen

Attractive salary and long-term job security

Up to 30 days vacation annually

Company pension scheme contributions post-probation

Social benefits including bonuses

Travel expense reimbursement

Tailored training and language courses

Qualifikationen

• Several years of experience in regulated product approval.
• Knowledge of drug approval is advantageous.

Aufgaben

• Planning and coordination of product approvals.
• Ensuring compliance with international regulations.
• Managing digitalization projects and implementing digital tools.

Kenntnisse

Project Management

English

Attention to Detail

Ausbildung

Scientific or Technical Studies

Tools

SAP

Digital Regulatory Tools

Jobbeschreibung

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

Our client, a global leader in skin care, cosmetics, and wound care, is seeking a Regulatory Affairs Specialist (m/f/d) in Hamburg to drive global product approvals and ensure compliance with international regulations.

Responsibilities include:

• Planning and coordination of product approvals
• Development and implementation of approval strategies
• Ensuring compliance with international regulations
• Compilation and review of approval documents
• Coordination with authorities and stakeholders
• Main contact for registration issues
• Establishing and maintaining approval systems
• Updating regulations compliance
• Managing digitalization projects and implementing digital tools

Qualifications:

• Completed scientific or technical studies
• Several years of experience in regulated product approval
• Knowledge of drug approval is advantageous
• Understanding of international regulations and standards
• Strong project management skills
• Excellent English skills (written and spoken)
• SAP knowledge is a plus
• Proficiency with digital regulatory tools
• High attention to detail and organizational skills

What We Offer:

• Attractive salary and long-term job security
• Up to 30 days vacation annually
• Company pension scheme contributions post-probation
• Social benefits including bonuses
• Travel expense reimbursement
• Open-ended employment contract
• Good prospects with our partners
• Tailored training and language courses