International QA Auditor
Job Summary
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.
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.
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.
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...)
Our culture is driven by values If this sounds like you youll fit right in:
Youre resilient and tackle challenges with a positive mindset
Youre curious and always up for learning something new
You have a no non-sense approach honest clear respectful
Youre innovative and bring ideas not just opinions
And above all youre serious about your work but not too serious about yourself
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 wont just be taking a job youll be joining a community where people grow laugh build and contribute to something bigger.
Interested Lets talk.
Send us your CV and motivation letter. You could be the next one to join the QbD family.