\\nAbout the role

74! The number of medical device projects in Novartis. Without a safe, user friendly, high-quality drug delivery system our patients cannot take their medicine. The Compliance, Systems and Operations team in Basel needs you to accelerate one of the most diverse and innovative medical device portfolios in the pharma industry. By creating opportunities for efficient data management for the device design history, you allow us to remove hurdles and enable agile development!

You\\\'ll be supporting data driven documentation, automations and improvement projects within the Technical Research & Development Device organization working within a cross-functional teams.

In addition, you will have the opportunity to contribute to the development and improvement of key processes for device development [in compliance with the EU Medical Device Regulations and ISO 13485 as well as US regulations 21 CFR Part 4 and 21 CFR Part 820] as well as contributing to the digital strategy.

Your responsibilities include, but are not limited to:

• Define and improve data model and database structure for medical device related information and data.
• Create, define or update search model for databases containing medical device data
• Working with stakeholders to identify inefficiencies and obstacles to leaner processes and digitalize them
• Help to create and/or improve procedures and processes to facilitate development of devices for Novartis.

Role Requirements

What you\\\'ll bring to the role:

• Master Student in Engineering, Biotechnology or Life Science, Computer Science or Computer Engineering. Quick learner, quality focused, good communication and collaboration skills, autonomous and self-driven.
• Knowledge in data structures and databases (e.g. SQL) as well as process automations (like Power Apps or Power Automate).
• Programming skills in Python, Xml, html, Java or similar programming languages.
• English both spoken and written is a must, German and French a plus.

Desirable requirements (optional):

• Medical device knowledge through university studies or direct work experience.
• Knowledge of regulatory standards for medical devices and/or combination products.
• Knowledge in statistics

Why consider Novartis?

743 million. That\\\'s how many lives our products touch. And while we\\\'re proud of that, 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 empowered to ask new questions, make bolder decisions and take smarter risks.

We are Novartis. Join us and help reimagine medicine.

Functional Area

Interns/Students on Novartis Payroll

Division

Global Drug Development

Business Unit

TECHNICAL R & D GDD

Employment Type

Internship

Commitment to Diversity & Inclusion:

We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Shift Work

No

Early Talent

Yes\\n \\n \\n \\n \\n \\n

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