Job Description Summary As a CMC development specialist, enhance Japan’s CMC development strategy by offering scientific and technical support to global/local CMC development teams and other departments, while keeping up with the latest technological advancements. Job Description Key Responsibilities Act as a subject matter expert (SME) on CMC development within the TRD submission team, from initiating clinical trials through NDA filings. Understand CMC development strategies for assigned projects and provide scientific and technical insights on potential risks, particularly for novel and complex elements. Develop expertise in new modalities and technologies, including formulations, process development, manufacturing and control strategies, and provide expert consultation. Provide input on Japanese requirements and expectations, and collaborate with local and global stakeholders to address scientific and technical challenges. Review and prepare documents, protocols and reports required for Japan filings and launches, including J-NDA Module 3 and J-QOS. Act as a CMC expert supporting other functions, including knowledge sharing, data generation for marketed products, and collaboration with clinical and commercial stakeholders. Maintain global and local development-related SOPs and manuals, and perform QC activities for investigational medicinal product (IMP) release in Japan. Ensure compliance with company requirements and, for manager-level positions, mentor associates and lead activities within PHAD Japan. Background Education: University or graduate (master's) degree (or higher) in pharmacy, science, engineering, or other technical fields. Essential Requirements University or graduate (master’s) degree or higher in pharmacy, science, engineering or another technical field. Expertise in at least one CMC area, such as drug substance, drug product, formulation development, process development, setting control strategy or analytical science. Basic knowledge of Japanese pharmaceutical regulations. Native-level proficiency in Japanese. Proficiency in reading and writing in English. Desirable Requirements Preferably 5+ years of experience in the pharmaceutical industry. Intermediate business-level speaking and listening skills in English. * You do not need to be familiar with all the modalities or technical area mentioned in the Major Accountabilities section. If you have specialized skills in any CMC area and a strong motivation to learn about other technical field, we encourage you to apply. Language skill: Native-level proficiency in Japanese is required, proficiency in reading and writing in English is necessary, and intermediate business-level speaking and listening skills in English are preferred. * If the candidate possesses exceptional CMC skills, the English language requirements mentioned above can be flexible and open to discussion. Benefits and Rewards Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf Commitment to Diversity and Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and Accommodation 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 diversityandincl.china@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Additional Information Be aware of fake job advertisements and job offers. Novartis does not make job offers without interviews and never asks candidates for money. All our current job openings are displayed here. If you have encountered a job posting or been approached with a job offer that you suspect may be fraudulent, we strongly recommend you do not respond, send money, or provide personal information. Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Skills Desired Continual Improvement Process, Master Data, Materials Management, Materials Requirements Planning (MRP), Production Planning, Supply Chain Management (SCM), Supply Chain Planning (SCP), Technical Requirements, Warehouse Management System (WMS), Waterfall Model Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. Novartis is aware of employment scams which make false use of our company name or leader’s names or recruiter’s names to defraud job seekers. Novartis does not make job offers without interview and never asks candidates for money. If you have encountered a job posting or been approached with a job offer that you suspect may be fraudulent, we strongly recommend you do not respond, send money or personal information. Novartis is not responsible for any claims, losses, damages, or expenses resulting from scams. In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov .

Associate or Manager, PHAD Japan.

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