Key Responsibilities

• Perform and document analytical testing on finished products, materials, and stability samples in accordance with GxP standards.
• Manage, store, and track samples to ensure traceability and accuracy.
• Conduct, interpret, and report microbiological monitoring within cleanrooms at the Baarle-Nassau site.
• Report technical complaints, deviations, or special situations within 24 hours of receipt.
• Maintain an orderly, safe, and compliant QC laboratory environment.
• Apply and follow safety, radiation, and laboratory regulations to prevent risks.
• Contribute to continuous quality improvement through proactive identification and solution-oriented actions.

Essential Requirements

• Bachelor’s degree in chemistry, biochemistry, microbiology, or a comparable life-science field.
• Fluent in English
• Strong knowledge of good laboratory practices and current Good Manufacturing Practices.
• Excellent analytical skills and strong attention to detail in documentation and laboratory processes.
• Openness to working with new technologies and a continuous improvement mindset.
• Clear, open, and effective communication with internal and external stakeholders.

Desirable Requirements

• Dutch language skills in addition to fluent English.
• Ability to act quickly and prioritize with a strong sense of urgency.

Commitment to Diversity and Inclusion:

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
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