REQ-10072931
Mar 03, 2026
LOC_NL
About the Role
Key Responsibilities
- Initiate and manage deviations to support compliant production processes.
- Lead investigations and perform thorough root cause analyses.
- Execute and track document changes to maintain process accuracy.
- Resolve first‑line production issues to ensure continuous operations.
- Support projects that strengthen production performance.
- Contribute to process optimization initiatives to enhance efficiency and quality.
Essential Requirements
- A completed vocational or bachelor’s degree in a technical or life‑science field such as Engineering, Biology, Medical Laboratory Research, or Chemical Analysis or similar area’s
- Practical experience within a pharmaceutical or controlled production environment.
- Strong analytical abilities to identify improvement opportunities and support root cause investigations.
- High attention to detail and accuracy in daily operations and documentation tasks.
Desirable Requirements
- Experience working in a Good Manufacturing Practice environment or in a production setting.
- Previous exposure to quality assurance processes or quality‑related responsibilities.
Commitment To Diversity And Inclusion
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Role Requirements
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.
Read our handbook (PDF 30 MB)
DIV_TO
Production / Manufacturing
LOC_NL
Baarle Nassau
NL42 (FCRS = NL042) IDB Holland BV
FCT_TO
Full time
Temporary (Fixed Term)
No