Consultant Regulatory Affairs (Senior o. Principal) In Vitro Diagnostic (m / f / x)

Entourage; Frankfurt; Hybrid; EUR 70.000 - 110.000; Vollzeit

Zusammenfassung

Join a forward-thinking consulting firm that is transforming the IVD industry. As a Senior or Principal Consultant, you will lead strategic regulatory projects, develop tailored solutions for complex challenges, and mentor junior consultants. This role offers the opportunity to engage with senior stakeholders and contribute to the continuous development of consulting methodologies. With a focus on regulatory affairs and quality management, you will be at the forefront of innovation and compliance in the diagnostics sector. If you are passionate about making an impact and thrive in a dynamic environment, this position is perfect for you.

Leistungen

Open corporate structure

Continuous development opportunities

Networking at IVD events

Flexible working environment

Qualifikationen

• 8+ years of experience in Regulatory Affairs or Quality Management in IVD.
• Deep knowledge of EU IVDR and FDA regulations.

Aufgaben

• Lead strategic consulting projects focusing on regulatory roadmap development.
• Manage projects and cross-functional teams ensuring compliance.

Kenntnisse

Regulatory Affairs

Quality Management Systems

Clinical Evidence

Strategic Consulting

Project Management

Communication Skills

German (C1 level)

English (C1 level)

Ausbildung

Degree in Natural Sciences

Jobbeschreibung

About the company and your impact at Entourage

Do you want to shape regulatory strategies and support the transformation of the IVD industry ? At Entourage, we partner with leading diagnostics companies to drive innovation, compliance, and growth.

Our IVD consulting team is looking for a Senior or Principal Consultant (m / f / x) in Munich / Remote, starting as soon as possible, to strengthen our strategic expertise in Regulatory Affairs, Quality Management, and Clinical Evidence .

About the role

• Regulatory Strategy & Consulting : You will lead strategic consulting projects with our clients, e.g. focusing on regulatory roadmap development, global registration strategies, gap assessments, and decision-making support for senior stakeholders. Your work will cover EU IVDR, FDA, and other key markets, including interaction with Notified Bodies and Competent Authorities.
• Analysis & Solution Development : You will develop tailored, forward-looking solutions for complex regulatory and quality-related challenges—ranging from performance evaluation planning to regulatory market access strategies.
• Execution & Leadership : You will manage projects and cross-functional teams, ensure timely and compliant implementation of regulatory or QA / clinical work packages, and act as a trusted advisor to our clients. As a senior expert, you’ll also mentor junior consultants and contribute to the continuous development of our consulting methodologies.

We are a match, if you have

• A degree in natural sciences or a comparable field of study
• Deep knowledge and strong interest in strategic regulatory affairs and QMS topics, especially in a global and evolving IVD environment
• More than 8 years of hands-on experience in RA and / or QA in the IVD industry, consulting, or Notified Body sector
• Proven experience in strategic work : RA strategy development, regulatory due diligence, IVDR transition, FDA submissions , or similar
• Solid understanding of the EU IVDR and FDA regulations, international registration pathways is a plus
• Experience with in-house IVDs / LDTs topics is a strong advantage
• Confident and engaging communication style ; ability to consult and influence at senior level
• C1 level German and English
• Willingness to travel (20-30% max.)

What we bring to the table

• An open corporate structure and equal communication
• An exciting environment and continuous development
• The chance to visit IVD events, networking in the IVD health world, while representing the Entourage at exhibitions, events, speaker events - or be the speaker yourself?
• Open salary structure depending on professional experience and education