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QMS facilitator
Aussicht: 135
Update Tag: 26-11-2025
Kategorie: Humanressourcen
Industrie: Pharmaceutical Manufacturing
Jobtyp: Full-time
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Jobinhalt
Job DescriptionAs part of the ‘Quality Management System team’ you need to ensure safe, effective and a timely supply of products to the market in compliance with regulated areas and Novartis standards and collaborate with the Global quality management system group.
Your responsibilities include, but are not limited to:
- You will be part of a team responsible for the quality of the products released on the market
- You will evaluate deviations from a compliance perspective and responsible for the reduction of recurrent deviations.
- You will participate in and/or lead investigation teams to give input towards regulatory products
- You will be responsible for defining the vital processes within the departments as referred to in the quality manual, regulatory requirements and Novartis standards
- Acting as subject matter expert during GMP audits and inspections; lead the preparation of responses to findings and the development and implementation of CAPAs
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Minimum Requirements
- A bachelor or master degree in Science (bio-engineer, chemistry, pharmacy,...).
- Excellent knowledge of Dutch and English (spoken and written).
- Accuracy, entrepreneurship and ability to work independently.
- Communication skills and capability of making contacts with different departments.
- Preferably a first experience within a Pharma regulatory environment.
We offer you an exciting, international and interdisciplinary work environment. Investment in people is a priority for Novartis. We offer a range of possibilities for personal development and career opportunities within the group to motivated, qualified people. We offer you a competitive salary and benefit package. Novartis also supports a flexible work-life integration (working remotely, flexi-time schedules, ...). Your office will be based in Puurs. Locally, we offer benefits to ensure our associate’s mental and physical well-being. There is a fitness available for our associates to use, and we offer a bike-leasing program. We have a mental mentor on site as well.
Why consider Novartis?
769 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives?
We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.
Imagine what you could do at Novartis!
Division
Novartis Technical Operations
Business Unit
NTO QUALITY
Country
Belgium
Work Location
Puurs
Company/Legal Entity
ALCON BEL
Functional Area
Quality
Job Type
Full Time
Employment Type
Regular
Shift Work
No
Early Talent
Yes
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Frist: 10-01-2026
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