Automation Engineer, Senior Specialist

Summary Novartis is at the forefront of transforming lives through radioligand therapy in nuclear medicine, combatting several prevalent cancer types. If you’re passionate about pushing the boundaries of this industry and creating innovative, life-saving medicines for cancer patients, consider joining us as a Global Automation Engineer, Associate Director. In this pivotal role, you’ll lead the development of cutting-edge Aseptic RLT automation systems using the latest technologies. The successful candidate will be responsible for ensuring the smooth operation of the OT scope of the automated lines across the network, managing the team effectively, and coordinating with cross-functional teams both locally and globally. Strong communication and leadership skills are required, as the TEMA lead will be responsible for interacting with the automated line vendor and ensuring that timelines and service level agreements (SLAs) are met. About the Role Your responsibilities will include: Act as a thought leader and influencer across teams in RLT, able to manage project teams and be a trusted partner for key stakeholders. Provide technical expertise for the design, configuration, installation, and maintenance of automation software and associated hardware; including interacting with other teams as necessary. Develop and implement strategies to optimize the performance, reliability, and efficiency of the OT systems used on the automated manufacturing lines. Strong Project management experience and ability to drive project teams to successful outcomes. Interact heavily with the Semi-Automated line vendor to ensure timely delivery, effective troubleshooting, and adherence to SLAs. What you will bring to the role: Bachelor's degree in Engineering, Computer Science, or a related field. 3 years of experience managing teams in IT or Automation, in a GMP Pharma environment. Experience in leading project teams and proficient in project management methodologies and tools. Strong leadership and decision-making abilities. Strong knowledge and understanding of automation systems, computer system validation, and regulatory requirements in the pharmaceutical industry. Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams. Fluent in English; Italian a plus. Desirable: Knowledge of radioligand therapy manufacturing processes and equipment is a plus. 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. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network. Restrictions on working flexibility may apply to this position and can be discussed at interview as required. Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerlandnovartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. J-18808-Ljbffr

Location: ivrea, IT

Posted Date: 11/25/2024