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

Entourage

Stuttgart

Hybrid

EUR 70.000 - 110.000

Vollzeit

Vor 9 Tagen

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Zusammenfassung

An established industry player seeks a Senior or Principal Consultant to drive innovation in Regulatory Affairs and Quality Management within the IVD sector. This role offers the opportunity to lead strategic consulting projects, develop tailored solutions for complex regulatory challenges, and mentor junior consultants. With a focus on global registration strategies and compliance, you will play a crucial role in shaping the future of diagnostics. Join a dynamic team that values equal communication and provides an exciting environment for professional growth, including opportunities to represent the company at key industry events.

Leistungen

Open corporate structure
Continuous development opportunities
Networking at IVD events
Flexible salary structure

Qualifikationen

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

Aufgaben

  • Lead strategic consulting projects for regulatory roadmap development.
  • Manage projects and mentor junior consultants.

Kenntnisse

Regulatory Affairs
Quality Management Systems (QMS)
Clinical Evidence
Strategic Consulting
EU IVDR Knowledge
FDA Regulations
Project Management
Communication Skills
Mentoring
C1 Level German
C1 Level English

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
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