Quality Assurance & Qualification and Validation Specialist

Location: Hybrid - Madrid
Type: Full-time

Are you the kind of person who wont rest until every system process and piece of equipment runs exactly as it should and can prove it

Were looking for a Quality Assurance & Qualification and Validation Specialist whos passionate about quality precision and ensuring that life-saving products are backed by rock-solid compliance.

In this hybrid role youll play a vital part in ensuring that critical equipment systems and quality processes meet the highest regulatory standards; from installation and performance qualification to batch release and continuous improvement. If you thrive on structure take ownership of quality outcomes and enjoy solving both technical and compliance challenges this could be the perfect next step in your career in the pharmaceutical or life sciences industry.

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.

Main responsibilities:

• Execute and document process validations (IQ/OQ/PQ) and test method validations in line with regulatory standards.

• Proactively identify critical process parameters and conduct risk assessments.

• Build hands-on GMP experience: review batch records support materials release and manage the batch release process.

• Lead nonconformance investigations and CAPAs ensuring clear action plans and timely resolution.

• Ensure data integrity and traceability across all quality records.

• Get exposure to audits & inspections: Support inspections and learn how to prepare documentation and interact with authorities.

• Prepare data-driven reports and present recommendations to management and stakeholders.

• Deliver hands-on training in validation and quality systems.

• Drive continuous improvement of quality policies and validation procedures.

• You bring a solid academic foundation with a BSc degree in Life Sciences Exact Sciences Computer Science or Engineering

• You have hands-on experience in QA computer system validation (CSV) or automated processes and a practical understanding of validating products equipment processes risk management and data integrity

• Youre confident navigating regulatory landscapes with working knowledge of GMP FDA EMA and local quality guidelines.

• Youre proactive results-oriented and flexible someone who pays attention to the details takes ownership and thrives both independently and in close collaboration with others

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.