About the Role

　　Location: Changshu

　　About the role:

　　Represents the main technical interface between Novartis and external suppliers by providing technical expertise on manufacturing and packaging process design, process- and cleaning-validation and resolution of technical issues. Applies an appropriate level of product and process oversight to ensure product quality and process robustness.

　　Key Responsibilities:

　　• Establish partnership with external suppliers with focus to ensure and improve product process capability, to keep the knowledge of process up to date and to maintain the product in constant state of validation.

　　• Product/Technical Stewardship for defined key molecules

　　• Responsible for the validation oversight and for maintaining the product in constant state of validation.

　　• Participate in external supplier / product evaluation and selection process. Responsible for gathering technical information on manufacturing process capability at external supplier.

　　• Ensure that new products and processes are well developed for the commercial scale and the entire product lifecycle at the commercialization site

　　• Support development of comprehensive control strategy early on in the development to ensure that validation requirements meet regulatory requirements and other critical metrics (e.g., quality, safety, environmental, cycle times, etc.).

　　• Define and execute design and control optimization projects where needed.

　　• Support implementation of applicable Novartis Manufacturing Manual practices.

　　Diversity & Inclusion / EEO

　　诺华致力于打造一个卓越、包容的工作环境和多元化团队, 代表我们服务的患者和社区。

　　Role Requirements

　　Key Responsibilities:

　　• BSc in pharmacy, pharmaceutical technology, chemistry or equivalent scientific degree. Desirable MSc. or PhD

　　• Fluent in English speaking and writing.

　　• Minimum 5 years of experience in pharmaceutical (chemical) manufacturing.

　　• Experience in a global/matrix environment in the pharmaceutical industry

　　• Comprehensive know how in pharmaceutical (chemical) technology

　　• Project Management experience

　　• Drug Development experience

　　• Sound experience of data handling and applied statistics

　　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! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

　　You'll Receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards

　　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 [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

　　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 here: https://talentnetwork.novartis.com/network. You can follow us via Novartis Group Recruitment WeChat Official Account and Novartis Group WeChat Video Account.

　　Division

　　Operations

　　Business Unit

　　SMALL MOLECULES

　　Location

　　China

　　Site

　　常熟

　　Company / Legal Entity

　　Novartis Pharma Beijing

　　Job Type

　　全职

　　Employment Type

　　正式员工

　　Shift Work

　　否