QbD Group

Young Graduate IFUcare

QbD Group  â€˘  Republic of Poland (Onsite)  â€˘  3 months ago
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Job Description

🔍 Young Graduate IFUcare

📍 Location Warsaw (Poland)
đź•“ Type Full-time

We are looking for a motivated and ambitious Young Graduate to join our innovative e-labeling software team at IFUcare IFUcare is a service provided by Qarad, a company within the QbD Group offering regulatory and quality expertise for medical devices (MD) and in vitro diagnostics (IVD) Our solution enables manufacturers to make paper Instructions for Use (IFU) electronically accessible, driving innovation, eco friendliness and compliance in healthcare.

💡 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

  • Serve as the first point of contact for our B2B clients, providing support for a wide range of inquiries, from general assistance to more complex cases.

  • Guide clients from start to finish, addressing questions related to quality systems, security, vendor management, regulatory compliance, and validation.

  • Collaborate with stakeholders such as regulatory, quality, IT, production and marketing to implement our solutions successfully.

  • Collect and analyze large amounts of information to apply effectively in your work.

  • Contribute to the continuous improvement of our services and ensure clients achieve success with our software.

  • Grow within the company, with opportunities to advance into roles such as technical sales, validation expert, project management or other specialties.

đź’Ş What you bring

  • You hold a master’s degree & are a recent graduate in a field related to science, technology, etc.

  • Your academic background is flexible as long as you are eager to learn and develop yourself.

  • Curious, self-reliant, and unafraid to dive deep into challenges. You see mistakes as learning opportunities.

  • Fluent in Polish & English, both written and spoken; additional languages are a plus.

  • Precise, detail-oriented, and tech-savvy, with a knack for software, digital tools, and systems. Looking for a role where you can think critically, take initiative, and contribute to innovation

🫵 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.

QbD Group

About QbD Group

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.

Industry
Consulting & Advisory
Company Size
501-1,000 employees
Headquarters
Antwerp, BE
Year Founded
Unknown
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