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Open nowPosted 71 days ago

International QA Auditor

qbdbv34 open roles

Where
Rubí, Spain
Work mode
Hybrid
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Your applicationOpen nowInternational QA Auditorqbdbv · Rubí, Spain

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The clock on this job

Early applications get read.

7.8% of postings close within 7 days. Measured by our own scanner across the market. qbdbv postings stay open a median of 1 days.

Share of postings closed within
  1. 1.6%1 day
  2. 3.4%3 days
  3. 7.8%7 days
  4. 14.3%14 days
  5. 33.7%30 days
This job: posted 71 days ago

qbdbv median: 1 days open

The posting

🔍 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.

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