Commissioning and Qualification Specialist
hace 2 días
Key Responsibilities:
• Execute commissioning and qualification activities based on expertise and GMP regulations for equipment in pharmaceutical production and drug testing.
• Identify, understand and define technical solutions for equipment.
• Develop commissioning and qualification plans together with other stakeholders within Novartis (users, quality).
• Performing Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT).
• Development and implementation of DQ, IQ and OQ protocols, in cooperation with equipment suppliers.
• Responsibility for personal professional development, gaining experience and competences.
• Implementing and following instructions and requirements to ensure safe working, protection of assets and the environment.
• Degree in engineering (Dipl. Ing. / M. Sc. / B. Sc.) or equivalent.
• Minimum 1 year of experience in engineering and/or production environment.
• Fluent in English and proficient in local language.
• Knowledge of Microsoft Office.
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. We are committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
Novartis is committed to work with and provide reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please let us know.
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