Job Description

Through the partnership with more than 1000 external suppliers, our network of 7 technology platforms provides our customers and patients in more than 150 countries with innovative, high-quality and affordable products -on time, every time, safely & efficiently. Your key responsibilities As a part of Quality departments in Novartis Technical Operations, you can contribute among different teams. Working as a Senior Manager, QRM Risk Analyst , you are responsible for managing cost effective GxP Compliance and/or Audit activities, operations, and systems to ensure compliance of business areas with the Novartis Quality Manual and Policies and all relevant GxP, legal and regulatory requirements, and through internal audits, KPIs (Key Performance Indicators) and KQIs (Key Quality Indicators). Leading the preparation and management of external and corporate audits and Health Authority inspections. Working as a Director, Global GxP and Quality Incident Management , your role is to drive the activities on global level. Global Leadership for and senior management of GxP and Quality Incidents (end to end management of escalated incidents, consistent assessments, initiation of corrections, appropriate closure), Severe Quality and Compliance issues, GxP/Quality Emergency situations (recalls, other market actions, Health Authority enforcements, counterfeits) and Health Authority interactions. Providing of GxP/Quality senior subject matter expertise to Sites, Functions, local and global entities, Country Affiliates, newly acquired companies related to GxP/Quality Incident corrective and preventive measures and driving of as well as senior global management of related activities (global CAPA plans, lessons learned, global cross-functional initiatives, workshops). Establishment of communication, trending and reporting of GxP/Quality incident details, the assessment of them as well as their compliance and regulatory impact. Ensuring that GxP/Quality incidents are being managed with efficient processes and in close collaboration with partners. Working as a Global QMS Specialist , your role is to support Quality Systems (GxP training system, document management system, document implementation process) in administration, reporting and communication. This is assured through completing tasks promptly, collaborating with team members in order to work effectively, and providing monthly reports. Imagine what you could experience at Novartis and learn more at Careers in Manufacturing and Supply | Novartis. Diversity & Inclusion / EEO Job 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. Minimum Requirements What you will bring to the role: . Minimum university degree in natural/technical sciences (e.g. as pharmacist, microbiologist or other biological science, pharmaceutical/chemical engineer, chemist, biochemist). . From 5 to 12 years of relevant professional experience (depending on the role) ideally gained in the pharmaceutical industry across various disciplines. Administrative experience in the Pharmaceutical GMP environment and pharmaceutical background would be beneficial. . Excellent command of English, with a second language preferred. . Ability to continuously foster holistic view over the project activities with strong risk awareness. Desirable Requirements: . Intercultural experiences and strong learning agility to work in complex and rapidly changing business environment. Excellent communication and organizational skills with ability to interpret and communicate complex information. . TrackWise, SharePoint, SAP and MS Office software tool knowledge is a plus. You\'ll receive Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, possibility to work from home, Pension scheme, Employee Recognition Scheme, Expanded program for the promotion of health in the field of physical, mental and social well-being (Energized for Life), employment at Top SI Employer, Unlimited learning and development opportunities. We offer permanent employment, with probation period. You are kindly invited to submit your application in English language, including CV. Why Novartis 766 million lives were touched by Novartis medicines in 2021, and while we\'re proud of this, we know there is so much more we could do to help improve and extend people\'s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what\'s possible, when we collaborate with courage to aggressively and ambitiously tackle the world\'s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse team\'s representative of the patients and communities we serve. Novartis is committed to working with and providing 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 send an e-mail to and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

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