đź“Ť Location Hybrid
đź•“ 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 a Toxicology Business Unit Manager to join our Madrid office and who will support the development and growth of the Toxicology Business Unit within the QA Division, working closely with Global Head QA.
The role combines scientific toxicology expertise with a strong quality mindset and a consulting-oriented approach (including commercial awareness and client focus) to support both technical excellence and business expansion.
The position acts as a key partner to the Global Head QA, contributing to the development of the service offering, supporting client projects, and identifying growth opportunities.
Technical & Scientific Contribution
Lead and contribute to toxicology consulting projects
Support and deliver work across the Toxicology service offering
Ensure scientific quality and regulatory alignment of deliverables
Operational Support
Support the day-to-day operational management of the Toxicology Business Unit
Help ensure projects and services are delivered effectively, consistently, and in line with client expectations
Contribute to the coordination and follow-up of activities to support smooth service delivery
Business Development Support
Support the growth of the Toxicology Business Unit
Contribute to:
Proposal preparation
Client discussions
Identification of new opportunities
Translate toxicology expertise into client-oriented solutions
Strategic Support
Support the Global Head QA in shaping the toxicology service portfolio
Contribute to identifying market opportunities
Support positioning of the company in toxicology consulting
• PhD / MSc in Toxicology, Pharmacology, Pharmaceutical Sciences and/or Life Sciences.
• More than 7 years’ experience in regulatory toxicology.
• Experience interacting with international clients and cross-functional teams is a strong plus. You need to be comfortable working in an international environment.
• Registration as European Registered Toxicologist (ERT) is a strong plus
• 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.
• The confidence to engage with business leaders and sales teams on financial matters, with clarity and without jargon.
• A genuine 'can do' attitude in ambiguous, fast-moving environments: you figure it out.
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.
The QbD Group supports life science companies worldwide throughout the entire product lifecycle – from idea to patient. We are a global company with over 700 high-qualified employees.
Our experienced team serves the wider life science industry, with a strong focus on ATMPs, medical devices, IVDs, and digital health, thanks to the specific expertise we have built in these areas. The services we offer fall under the following divisions:
• Regulatory Affairs: We help our clients in their journey throughout the entire drug and medical device regulatory lifecycle.
• Clinical: We are an expert clinical solutions provider specialized in medical devices and biotech, offering global CRO services and consultancy.
• Qualification and Validation: We guarantee that products meet quality demands and comply with regulation through the qualification and validation of your processes, equipment, and software.
• Quality Assurance: We offer the full range of QA services necessary to get your product to market in a safe and compliant way, including auditing from certified auditors, setting up your QMS, and all QP (Qualified Person) activities.
• Quality Control: Our QC division consists of a GMP laboratory that offers analytical services for testing pharmaceutical raw materials, excipients, and release testing of finished products.
• Software solutions: Cloud-based and pre-validated Quality Management Software built for the life sciences, as well as eIFU services which enable IVD and MD manufacturers to digitalize paper Instructions For Use (IFU).
• Go to market: We help you launch your product to market by providing marketing and communication services, business development support and sales strategy.
