And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. That a diverse, equitable and inclusive environment inspires new ways of working. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. Significant QC and AS&T experience within Novartisħ69 million lives were touched by Novartis medicines in 2020, 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.Fluent in English and good knowledge in German and/or French is a plus.Proven understanding of pharmaceutical cGMP and regulatory aspects of biological and sterile products.Strong interpersonal skills and ability to effectively lead through influence without formal authority. Advanced problem-solving skills and ability to connect to strategy and long term planning. Cross-functional business understanding from Technical R&D, operations, quality, finance and organizational set-up/design.Minimum of 7 years managerial experience in a pharmaceutical or biotech operational environment, with Quality Control experience.Technical degree in biotechnology or other pharmaceutical or life science related scientific degree with additional qualification in economics is desirable.Identifies/implements Compliance & Productivity initiatives across Analytics Labs (eg Lean Lab, TM Improvement Program), provides troubleshooting support and expertise to QC/AS&T functions in the sites and participates as needed in investigations (deviations, forensic, etc.).Maintains awareness of regulatory requirements affecting the pharmaceutical industry Defines & enforces current standards, procedures and Quality modules and directives, GOP for Analytical Laboratories as required.Drives global standardization/integration of analytical business processes and information, data, global equipment standards and application architecture across the platform, evaluating the implementation of new technologies/systems/software.Provides technical expertise and direction for the purpose of regulatory submissions and supports business development and licensing evaluations.Indirect leadership of the Manufacturing site QC and AS&T heads at all manufacturing sites.Creates QC and AS&T strategic plan (technologies, locations, etc.) and implementation of plan for the Large Molecule Quality Control Labs.Your responsibilities include, but are not limited to: In addition, you will be a key person in developing and executing our QC testing strategy in the Large Molecules network (including ESO and CMO activities). More than 3000 associates of more than 100 nationalities in Large Molecules Platform that deliver high quality and affordable medicine on time, every time, safely and efficiently.Īs Head QC/AS&T Head of Large Molecules, you will be responsible for oversight of the Quality Control/Analytical Science & Technology in our manufacturing sites and a key interface between Technical Research and Development Organization and Novartis Technical Operations. Global Head QC/AS&T Large Molecules (f/m/d), Novartis Technical Operations, Schaftenau, Austria
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