Sourcing Statement You are applying to be part of the Novartis Talent Pool. We are not currently recruiting for this role but we are building a pipeline for future opportunities. If you would like to be considered for a similar position in future, then please submit your CV.

Job Description
Quality is our key priority every day and in every aspect of our work. It is integrated in our daily work, demonstrated by the trust and respect of employees, patients and business partners. For many years successful assessments by regulatory authorities from countries around the world have confirmed it. We achieve high quality standards in all work processes, in the development and production of medicines and in the supply of markets. Our highly trained and experienced professionals play a key role in this.

Join us in the Quality department and you will take on planning and analytical studies (development, method validation, transfer of methods) and contribute to development, implementation and verification of compliance of internal quality systems in order to mitigate the risks associated with the quality of products/active ingredients, and to reduce the costs due to poor quality, in accordance with the law, good practices and business objectives.

Your key responsibilities
• Responsible for the development of the internal quality systems in accordance with the pharmaceutical laws and regulations, Good Pharmaceutical Practices, and Novartis standards.
• Ensure compliance in activities and GMP regulation with Novartis standards.
• Involvement in internal and external inspections.
• Responsible for validation of technical-technological documentation.
• Constantly develop and learn regarding Good Pharmaceutical Practices.
• Responsible for validation of products, processes, systems.

Minimum requirements
Your key responsibilities
• Responsible for the development of the internal quality systems in accordance with the pharmaceutical laws and regulations, Good Pharmaceutical Practices, and Novartis standards.
• Ensure compliance in activities and GMP regulation with Novartis standards.
• Involvement in internal and external inspections.
• Responsible for validation of technical-technological documentation.
• Constantly develop and learn regarding Good Pharmaceutical Practices.
• Responsible for validation of products, processes, systems.

What you will bring to the role
• BSc. in Pharmacy, Pharmaceutical Technology, Chemistry or equivalent scientific degree.
• Fluent in English.
• Knowledge of Microsoft Office.

Desirable Requirements
• 1 year of working experience in comparable positions.

We expect responsible, communicative people, who are focused on teamwork, achieving results and who are ready to accept new challenges and strive to expand their knowledge.

You are kindly encouraged to submit your application in our candidate data base. If we recognize you as potentially suitable candidate (m/f/d) for some of the open roles in Quality, we'll contact you.

Why consider Novartis?
750 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.

We are Novartis. Join us and help us reimagine medicine.

Commitment to Diversity & Inclusion:

Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.