International QA Auditor
qbdbv
| Company | qbdbv |
| Category | Engineering |
| Location | — |
| Remote | — |
| Employment | Not stated |
| Level | Not stated |
| Salary | Not stated by the employer |
| Posted | 23 Jul 2026 |
| Last verified | 11 Aug 2026 |
| Source | Employer ATS (teamtailor) |
Description
🔍 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.