Key Responsibilities:

• Preparation and execution of production of radio pharmaceutical products.
• Checking all quality requirements of the products within a GMP environment.
• Maintaining batch documentation and writing deviations.
• Optimizing the production processes by actively setting up and proposing points for improvement.
• Performing validation work.
• Remedying first-line failures.

Essential Requirements:

• MBO or HBO degree (Engineering, Biology and Medical Laboratory Research, or Chemical Analyst) or in a similar field, MTS or MLO.
• Knowledge of a pharmaceutical or control production environment.
• Analytical skills that allow you to see what can be improved.
• Attention to detail.

Nice to have/ Desirable Requirements: 2 bullet points maximum (optional)

• Experience with production or GMP is an advantage

Why Novartis

Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we

Achieve This? With Our People. It Is Our Associates That Drive Us Each Day To Reach Our Ambitions. Be a Part Of This Mission And Join Us! Learn More Here

http://www.novartis.com/about/strategy/people-and-culture

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.

Join Our Novartis Network

If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about

Novartis and our career opportunities, join the Novartis Network here: http://talentnetwork.novartis.com/network