Quality Assurance Specialist - NL

🔍 Quality Assurance Specialist NL

📍 Location: Hybrid, NL

🕓 Type: Full-time

Are you passionate about delivering exceptional quality and driving continuous improvement? We are looking for a detail-oriented and proactive Quality Assurance Specialist to join our team. In this role, you will play a key part in ensuring our client's products and processes consistently meet the highest standards. If you thrive in a collaborative environment, have a keen eye for detail, and are committed to excellence, this could be the next step in your career

💡 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

• Generate, and maintain Quality records in support of the Quality Systems

• Prepare detailed reports and present data-driven recommendations to management and stakeholder

• Conduct risk assessments and proactively identify critical process parameters and potential failure points

• Investigate deviations, non-conformities, and customer complaints using root cause analysis and risk-based corrective and preventive actions (CAPA)

• QA batch record review, support materials release and support batch release process.

• Support regular audits and inspections to verify that processes consistently operate within defined design spaces and comply with internal standards and external regulations

• Collaborate cross-functionally to design, validate, and optimize processes that consistently deliver products meeting quality attributes

• Ensure quality requirements are incorporated from development through production, supporting lifecycle management.

• You keep your knowledge within your expertise up to date with the latest guidelines, methodologies, and trends.

💪 What you bring

• You bring a solid academic foundation with a Bachelor or Master degree in pharmacy, bioengineering, biomedical sciences, or applied sciences.

• Hands-on experience in QA in a GMP environment, preferably in a commercial GMP manufacturing setting

• A keen eye for detail and product quality is your main concern. You think and act in a structured way, are flexible and stress resistant

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

• You have an excellent command of both Dutch and English, with strong written and verbal communication skills.

🫵 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.