International QA Auditor

Posted 2 Months Ago
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Rubí, Barcelona, Cataluña, ESP
Hybrid
Senior level
Professional Services • Biotech • Consulting • Pharmaceutical
The Role
Perform on-site and remote GxP/ISO 13485/MDR/IVDR audits worldwide, produce and follow up audit reports, provide corrective recommendations, support clients in remediation, and maintain up-to-date regulatory knowledge.
Summary Generated by Built In
🔍 International QA Auditor

📍 Location: Barcelona, Spain
🕓 Type: Full-time

We are currently looking to expand our network of Experienced QA Auditors to support occasional, international assignments within the pharmaceutical, biotech, and medical devices industries.

This is a role, ideal for QA professionals who value flexibility and international exposure.

💡 What’s in it for you?

Make a real impact: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devices

Grow within a community of experts: Benefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your expertise.

Build a meaningful career: As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences.

A fair, competitive package: We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations — because your contribution deserves to be valued.

🏢 What you’ll be doing
  • Conduct on-site and remote audits at client sites or suppliers worldwide

  • Perform audits in compliance with applicable standards and regulatory requirements (GxP, ISO 13485, MDR/IVDR, etc.).

  • Prepare, issue, and follow up on audit reports within agreed timelines

  • Provide expert recommendations and support clients in addressing findings.

  • Maintain up-to-date knowledge of industry regulations and standards.

💪 What you bring
  • Minimum 8 years of QA experience in the pharma, biotech, or medical devices sector.

  • Proven experience conducting international audits with certified lead auditor accreditation.

  • Excellent knowledge of relevant regulations: GxP, ISO 13485 and/or MDR/IVDR .

  • Fluent in English; any additional European languages (Spanish, German, Polish, French,...) is a plus.

  • Strong communication, organization and reporting skills

  • You are quality-oriented, meticulous and customer-oriented

  • Flexible and willing to travel occasionally within Europe or internationally (US, China, South of Asia,...)

🫵 Who you are

Our culture is driven by values If this sounds like you, you’ll fit right in:

  • You’re resilient and tackle challenges with a positive mindset

  • You’re curious and always up for learning something new

  • You have a no non-sense approach honest, clear, respectful

  • You’re innovative and bring ideas, not just opinions

  • And above all, you’re serious about your work, but not too serious about yourself

✨ About us

We support life sciences companies from idea to patient — offering tailored solutions in development, clinical, regulatory, compliance, production, and distribution. With 500+ experts across 8 countries, we help drive innovation in ATMP, biotech, medical devices, diagnostics, digital health, and pharma.

We believe in JPEG:
Joy. Partnership. Going the Extra Mile. Getting Things Done.

You won’t just be taking a job — you’ll be joining a community where people grow, laugh, build, and contribute to something bigger.

📩 Interested? Let’s talk.
Send us your CV and motivation letter. You could be the next one to join the QbD family.

Skills Required

  • Minimum 8 years of QA experience in pharma, biotech, or medical devices
  • Proven experience conducting international audits with certified lead auditor accreditation
  • Excellent knowledge of relevant regulations (GxP, ISO 13485, MDR/IVDR)
  • Fluent in English
  • Additional European languages (Spanish, German, Polish, French, etc.)
  • Strong communication, organization, and reporting skills
  • Quality-oriented, meticulous, and customer-oriented mindset
  • Flexible and willing to travel occasionally within Europe and internationally
Am I A Good Fit?
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The Company
HQ: Wilrijk
700 Employees
Year Founded: 2011

What We Do

QbD Group is an international life sciences consultancy supporting companies from idea to patient. It provides tailored solutions across development, clinical services, regulatory affairs, quality and compliance, production, distribution, and related software. The company serves advanced therapies, biotech, medical devices, diagnostics, digital health, and pharmaceutical organizations, helping clients accelerate innovation, achieve regulatory compliance, and grow with operational confidence across global markets.

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