Suppliers Quality Management Specialist - BCN at QbD Group
Rubí, Catalonia, Spain -
Full Time


Start Date

Immediate

Expiry Date

17 Jun, 26

Salary

0.0

Posted On

19 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Quality Management, Specification Coordination, Drawing Review, Quality Contracts, Database Management, KPI Monitoring, Documentation Management, Certificate Management, Excel, Power BI, SAP

Industry

Business Consulting and Services

Description
🔍 Job Title 📍 Location: Barcelona 🕓 Type: Full-time Introduction text 💡 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 Coordination of specifications and drawings with suppliers Review of quality contracts Database management and maintenance Creation and monitoring of KPIs Management of documentation and certificates with suppliers. 💪 What you bring Education: Technical background (Chemistry, Engineering, Biotechnology, etc.) Experience: Previous experience in the listed tasks, preferably in an SQM department. IT Skills: Proficiency in Excel and Power BI (SAP is a plus). Languages: Good level of English to draft and interpret technical documentation. 🫵 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.
Responsibilities
This role involves coordinating specifications and drawings with suppliers, reviewing quality contracts, and managing documentation and certificates. Key activities also include database maintenance and the creation and monitoring of Key Performance Indicators (KPIs).
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