regenold GmbH
  • Solutions
    • By Product Type:

      • Pharmaceuticals
      • Biologicals, Biosimilars & ATMPs
      • Medical Devices
      • In Vitro & Companion Diagnostics
      • Digital Health & SaMD
      • Combination Products
      • Borderline Products
      • Food & Cosmetics

      Keep Your Drug-Device Combination Products Variation-Ready

      We’ve experienced, that even long established drug–device combinations can fall short of current regulatory data expectations—putting variations at risk. We support you in assessing and strengthening your DDC data package to ensure robust, compliant submissions.

      DDC Variation Readiness

      EU Submission Readiness for Global Pharma

      Avoid Late Surprises in Your EU Submission. FDA approval is not a guarantee of EU readiness. European regulators apply different expectations for data, documentation, and operational infrastructure. Many US companies encounter gaps that lead to delays, rework, or regulatory friction.

      EU Readiness Checks

      SPOTLIGHT: EU AI Act Q&A Competition

      From May to June 2026, we are hosting the first competition to assess the ability of AI agents to answer truthfully, concisely, and effectively to questions of the AI Act.

      AI Act Competition
  • Services
    • Regulatory Affairs:

      • Regulatory Strategy & Operations
      • Regulatory Intelligence
      • Medical Device & IVD Regulatory Services
      • Software as a Medical Device & Cybersecurity
      • Product Information, Labelling & Promotional Compliance
      • Regulatory Compliance Roles & Legal Representation

      Development & Science:

      • Preclinical Development
      • Pharmaceutical Development & CMC
      • Clinical Development
      • Medical & Scientific Writing

      Quality, Compliance, & Data:

      • Quality & Compliance
      • Risk Management & Human Factors
      • AI Governance & Compliance
      • Data Protection & Information Security

      Pharmacovigilance & Safety:

      • Pharmacovigilance & Device Vigilance

      Commercial & Lifecycle:

      • Market Access & HTA Strategy
      • Post-Approval & Lifecycle Management
      • Due Diligence Support

      Strategic Advisory:

      • Strategic Advice
  • Focus Areas
    • Focus Areas:

      • Pharmaceutical Development
      • Medical Devices & IVDs
      • Digital Health & SaMD
      • AI in Regulated Life Sciences
      • Due Diligence
      • Entry into Europe
      • Food & Cosmetics → nutracompliance.com

      Keep Your Drug-Device Combination Products Variation-Ready

      We’ve experienced, that even long established drug–device combinations can fall short of current regulatory data expectations—putting variations at risk. We support you in assessing and strengthening your DDC data package to ensure robust, compliant submissions.

      DDC Variation Readiness

      EU Submission Readiness for Global Pharma

      Avoid Late Surprises in Your EU Submission. FDA approval is not a guarantee of EU readiness. European regulators apply different expectations for data, documentation, and operational infrastructure. Many US companies encounter gaps that lead to delays, rework, or regulatory friction.

      EU Readiness Checks

      SPOTLIGHT: EU AI Act Q&A Competition

      From May to June 2026, we are hosting the first competition to assess the ability of AI agents to answer truthfully, concisely, and effectively to questions of the AI Act.

      AI Act Competition
  • Resources
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    • Who We Are
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    • Careers
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    • UK
    • Ireland
    • Portugal
  • Contact

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We look forward to hearing from you.

regenold GmbH
Arrange a Call

Headquarters:
regenold GmbH
Zöllinplatz 4
79410 Badenweiler
Germany

Phone: +49 7632 82 26-0
Fax: +49 7632 82 26-555
Email: info@regenold.com

  1. Home
  2. About
  3. Careers

Careers

Build Your Future With Us

We are always looking for talented people who want to work at the forefront of life sciences and healthcare, supporting clients from early development through to regulatory approval and market access.

Join a team where expertise, collaboration, and curiosity come together to deliver meaningful impact for our clients and patients they serve.

Working at regenold

Our strength lies in our people. We bring together specialists across development, regulatory, and market access who work collaboratively to solve complex challenges and deliver tailored solutions.

We foster a culture built on partnership, open communication, and respect for each individual’s expertise and perspective.

You’ll be part of a supportive, international environment where your contribution is valued and your ideas are encouraged.

What Makes Us Different

A collaborative culture.

We believe the best outcomes come from working together. Our teams share knowledge openly, challenge ideas constructively, and support one another to succeed.

Global expertise.

You’ll work as part of an international network spanning over 90 countries, gaining exposure to diverse projects, clients, and regulatory landscapes.

Meaningful work.

From early development to market access, your work will contribute to bringing healthcare products to patients worldwide.

A people-first mindset

We value every individual’s skill and experience, creating an environment where everyone can thrive and grow.

What We Offer

Flexibility and autonomy.

We offer flexible, modern ways of working with the trust and freedom to manage your time and responsibilities.

Career development.

We support your growth through structured onboarding, tailored training, and long-term career opportunities.

International experience.

Work across borders, collaborate with global experts, and gain exposure to a wide range of projects and disciplines.

Supportive environment

Flat hierarchies and open communication enable fast decision-making and a strong sense of team connection.

Our Teams

Our work spans the full healthcare product lifecycle, with opportunities across:

  • Regulatory Affairs
  • Clinical and Preclinical Development
  • Pharmacovigilance
  • Quality and Compliance
  • Medical Devices and Diagnostics
  • Market Access
  • Project Management and Scientific Services

Our teams collaborate seamlessly to deliver integrated, end-to-end solutions.

A Diverse and Inclusive Workplace

We are proud to be a diverse, international organisation, bringing together people from a wide range of backgrounds, experiences, and perspectives.

We believe diversity drives better thinking, stronger collaboration, and better outcomes for our clients and partners.

Our Commitment

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We are committed to fair, transparent, and inclusive recruitment. If you require any adjustments during the application process, we will support you every step of the way.

Come Join Us!

We are always interested in hearing from motivated individuals who want to make an impact. Whether you are at the beginning of your career or bringing years of experience, you will find opportunities to grow, contribute, and succeed.

Explore our current job opportunities

For current opportunities in the UK and Ireland, please click here.

Page Contents

  • Working at regenold
  • What Makes Us Different
  • What We Offer
  • Our Teams
  • A Diverse and Inclusive Workplace
  • Our Commitment
— CELEBRATING 30 YEARS OF INNOVATION AND EXCELLENCE IN LIFE SCIENCES —
regenold GmbH

regenold is a global, end-to-end integrated development partner for pharmaceuticals, medical devices, and drug-device combination products. We support life sciences companies across the entire product lifecycle, delivering integrated development, regulatory, and market access expertise to enable efficient, compliant advancement from concept to market.

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regenold GmbH
Zöllinplatz 4
79410 Badenweiler
Germany

Phone: +49 7632 82 26-0
Email: Email Us

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