REQ-10029622
Nov 13, 2024
China

About the Role

Key Responsibilities

  • Has operational end-to-end responsibility within the Local Supply Center for material supply of the assigned projects. Represents the Supply Center in CHAD and PHAD project subteams. Influence process development by providing expertise in scaling up the chemical processes in order to develop mature and robust processes and prepares and execute launches at TechOps when appropriate.
  • Represent LSC in CHAD and PHAD project subteams and serve as the main contact between the CDU and LSC for the assigned projects.
  • Operational end-to-end responsibility for material supply of the assigned projects within LSC
  • Work frequently on several projects simultaneously.
  • Plan, prepare and execute assigned process steps/campaigns within the Supply Center according to Dev. Manual guidelines and internal regulations (GMP and HSE) while meeting project team targets
  • Actively contribute to process development by providing expertise in scaling up the chemical processes in order to develop mature and robust processes.
  • Prepare and execute launches and validation campaigns at TechOps and give on-site support as assigned.
  • Represents Supply Center in project specific approval audits by authorities (e.g. PAI) 

Essential Requirements:

  • Professional experience (ca. 3-5 years) in GMP environment and analytics (e.g., Quality Control)
  • English ability is a must
  • Master or Doctorate degree of related area

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

 

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

 

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: 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. You can follow us via Novartis Recruitment WeChat Official Account and Novartis Recruitment WeChat Video Account.

Role Requirements

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

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

Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Development
Innovative Medicines
China
Changshu (Jiangsu Province)
Research & Development
Full time
Regular
No
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REQ-10029622

Senior Expert Science & Technology - I

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