Associate Consultant Toxicology

📍 Location: Hybrid - Madrid
🕓 Type: Full-time

QbD Group is a pan-European life sciences consultancy with 600+ experts across 8+ countries, helping pharmaceutical, biotech and medtech companies bring their products to patients: fast, compliance and with confidence. We are in an active phase of national and international growth, which makes our Toxicology team more important than ever: you keep the engine running while we scale.

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.

We are looking for an Associate Toxicology to join our Madrid office and who will support the day-to-day work of the toxicology team, with specific experience in preparing PDEs and OELs.

The role combines scientific toxicology expertise with a strong quality mindset and a consulting-oriented approach to support both technical excellence and business expansion.

Specific Responsibilities:

- Reading of reports and scientific texts for the integration of technical criteria.

- Management of scientific bibliographic databases.

- Review of articles and toxicological studies.

- Attending in specific meetings related to their area of work.

- Preparation of reports.

- Participation in specific meetings related to their area of work.

• PhD / MSc in Toxicology, Pharmacology, Pharmaceutical Sciences and/or Life Sciences.

• More than 2 years’ experience in toxicology.

• Good analytical skills, attention to detail and ability to manage multiple tasks and priorities at the same time is considered a plus.

• Experience interacting with international clients and cross-functional teams is a strong plus. You need to be comfortable working in an international environment.

• Experience in preparing PDE and OEL reports and toxicological assessments.

• Excellent oral and written communication skills in both English and Spanish are non-negotiable: you switch between the two daily, across internal teams and international stakeholders. Any additional European language is a welcome bonus.

• A process-oriented mindset: you do not just solve problems, you fix the system so they do not happen again.

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

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.