Technical Steward - Kurtköy

Summary

You will be responsible for acting as the single point of contact for global MS&T and technical development initiatives at our site in Kurtköy, Istanbul. You will maintain deep knowledge of local manufacturing technologies, including scale‑up/down processes and Design of Experiments (DoE). You will provide technical expertise to support validation activities and ensure compliance. Additionally, you will drive harmonization and optimization of technical processes across the site to enhance efficiency and consistency.

• Act as single point of contact for global MS&T and technical development.
• Own knowledge of local manufacturing technologies, including scale‑up/down and DoE.
• Provide technical expertise for validation activities.
• Harmonize and optimize technical processes across the site.

• BSc. in Pharmacy, Pharmaceutical Technology, Chemistriy or equivalent scientific degree
• Desirable MSc. or equivalent experience
• Minimum 8 year experience in GMP manufacturing relevant to the specialist area of expertise
• Proven process understanding (Pharma, GMP, Regulatory aspects)

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:

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Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.

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Seniority level:
Mid‑Senior level.

Employment type:

Full‑time. Job function:
Engineering and Information Technology. Industries:
Pharmaceutical Manufacturing.