Regulatory Affairs Specialist (m/f/d) (Pharmaceuticalist)

Connecting people and technologies, creating the Perfect Match for our customers, always finding the right experts for the respective challenge - that is our ambition at FERCHAU and that is why we are looking for you: As an ambitious colleague who, like us, wants to take technologies to the next level. As an experienced professional, you support your colleagues with your many years of know-how and your expertise.

These are the challenges you will take on

• Coordination and implementation of product approvals in the EU and on international

markets

• Preparation of registration documents
• Support for the development department in the creation and maintenance of product files
• Participation in the introduction of new processes (MDR 2017/745)

These are your perspectives for the future

• Individual career guidance through dialogue-oriented supervisor feedback
• Development of cross-functional competencies
• Individual career programs for your development

Convince us with your qualifications

• Successfully completed technical or scientific studies or comparable

qualification

• Knowledge in the field of product approval of medical devices and regulatory

requirements (e.g., MPG, MDD, AIMDD, FDA)

• Knowledge of the standards ISO 13485, ISO 14971, IEC 60601-1/2, IEC 62304 is an advantage
• Experience in the preparation of Technical Documentation
• Good English language skills

Is our offer made for you? Then we look forward to your application - preferably online under the reference number VA93-97730-FR to Ms. Laura Kasimirski. We match: your potential and our possibilities. Challenge accepted? Let's start the next level together and develop the future!