📍 Location Hybrid
đź•“ Type Full-time
QbD’s team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD. We are always looking for the next QbD’er.
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.
Start strong with a dedicated onboarding week
When you join as a Young Potential, you kick off your journey with an intensive training week focused on the different facets of the product lifecycle in the life sciences industry. You’ll gain a solid theoretical foundation, combined with practical examples and real-life applications that you can immediately use in your projects with clients.
In addition, you’ll receive training to strengthen your interpersonal skills, such as communicating with impact. This will help build the confidence you need to successfully start your first assignments.
👉 Our upcoming onboarding weeks are scheduled beginning of September and mid-October
Under the mentorship of QbD, you'll have the opportunity to take your first professional steps in the fields of Quality, Qualification and Validation (including equipment, process, software, new product integration, ...).
You'll work within companies in the Life Sciences sector: pharmaceutical, biotech and medical devices, ranging from well-established companies to the newest and most innovative start-ups.
In line with the strict regulations of these sectors, you'll provide support on:
Managing quality-related risks during product development, production and distribution
Validating procedures, processes, and systems
Improving existing and setting up new quality management systems
Optimizing technology transfer and supporting new product launches
A master’s degree in a life sciences-related field (industrial engineering, civil engineering, bioengineering, industrial pharmacy, biomedical sciences, biotechnology/biochemistry, chemistry, or a similar scientific field)
Fluency in Dutch and English.
An entrepreneurial and communicative mindset
Eagerness to learn and an open mind
Flexibility and a willingness to go the extra mile
Our culture is driven by values. If this sounds like you, you’ll fit right in:
Resilient, with a positive mindset
Curious and eager to learn
No-nonsense: honest, clear, and respectful
Innovative: you bring ideas, not just opinions
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 fill in our quick JPEG questionnaire to check if you fit the QbD values.
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.