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Technical Manager (REQ-10087234)

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Onsite

Technical Manager (REQ-10087234)

Chengdu Kanghong Pharmaceutical Group Co.,Ltd.

Technical Manager (REQ-10087234)

Skills

Testing & QASupply ChainComplianceRegulatory Compliance

8 days ago

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Important information


Contract type:

Internship

Salary:

CN¥324,000 – CN¥492,000 / year

Location:

Suzhou, Jiangsu, China

Work mode:

Onsite

Published on:

15 October 2026

What they need


该职位来源于猎聘

  • Subject Matter Expert of specific pharmaceutical processes, having a complete understanding of them and assuring a seamlessly operation of the Manufacturing Science and Technology (MS&T) strategies and objectives.
  • 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.
  • Performs the technical due diligence in pre-evaluation phase to select the appropriate external suppliers together with BD&L.
  • Acts as responsible Technical Transfer Lead to facilitate Product Transfers for legacy products as well as new development products from Novartis to external suppliers or between external suppliers. Aligns with the Development organization for manufacturing process design during early-stage development
  • Acts as the MS&T representative in assigned Supplier Relationship Team (SRT). Provides technical / scientific process support to respective Supply relationship teams (SRT) and works in close relation with other SRT members (QA Managers, AS&T Managers, Life Cycle Managers , Supply Chain Managers, Site Change Coordinators, Supply relationship Manager etc.) for evaluation of technical compliance activities (Deviations, Change controls, Customer Complaints, CAPAs). Ensures seamless flow of knowledge and information transfer within the organization and across functions with focus on process and product know-how. Major accountabilities:
  • Responsible for technology transfer activities at site level (within, inbound and outbound), including any scale-up or other process adaptations.
  • Leads technical transfer project team at site and liaises efficiently with involved functions (e.g. Technical Development, Supply Chain, Production Unit, Quality Control, HSE, other sites.).
  • Owns the process knowledge of the product(s) assigned throughout the commercial lifecycle, maintains the oversight on process capability, through data trending and statistical analysis of critical variables, ensuring process(es) are robust, in continued state of validation and continuously improving.
  • Ensures seamless flow of knowledge and information across functions, and with other Sites when applicable, with focus on the assigned product(s).
  • Oversees processes and standards to maintain and improve existing and to implement new innovative manufacturing technologies when applicable.
  • Responsible for developing, implementing and managing the site process validation, primary packaging validation, cleaning validation and revalidation strategies to meet cGMP and quality requirements on time and on budget to ensure that programs are aligned with Regulatory Authorities’ expectations and related SOPs.
  • Design, plan, perform, interpret and report scientific experiments under the lead of the department head to contribute to overall MS&T strategies and objectives. Scientist MS&T
  • Complex projects with deep understanding of development process requirements
  • Difficult to solve topics (eg. new by-product investigation, complex deviations)
  • Cross product alignment in support approach (larger sites)
  • Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt
  • Distribution of marketing samples (where applicable) Education:
  • Higher scientific degree in Pharmacy, Pharmaceutical Technology, Chemistry or equivalent scientific field. Languages:
  • Fluency in English languages.
  • undefined Experience:
  • Minimum 5 years of experience in pharmaceutical (chemical) manufacturing and in sterile drug product manufacturing , with a comprehensive know-how in pharmaceutical technology Compentency
  • Applied Business Insights
  • Operational Excellence
  • Project Excellence
  • Manufacturing Process/Product Expertise Key performance indicators:
  • Cost, C-Sat and productivity targets
  • Achievement of project plans & milestones
  • Internal customer satisfaction with quality of services provided 为什么选择诺华:帮助患者及家属不仅需要创新科学,还需要一支包括你我他在内的充满智慧与激情的团队,大家相互协作、支持与激励。共同实现突破,改变患者的生活。一起共创更好的未来,你准备好了吗? 薪酬与福利:您可以前往诺华官网了解我们帮助您实现个人与职业发展的举措。 无障碍及便利设施: 诺华承诺与残障人士共事并为他们提供合理的便利设施。如果您由于健康状况或残障,在招聘过程的任何环节需要合理便利设施,或者为了履行职位的基本职能,请将您的相关需求告知我们的招聘经理。 加入我们的诺华网络:这不是您心仪的职位?欢迎加入诺华人才社区,与我们保持联系,及时了解合适的职业机会。您也可以关注诺华招聘社交媒体账号。 职位要求: Operational Excellence Technical Leadership Regulatory Compliance Applied Statistics Manufacturing Technologies Technology Transfer Process Control Quality Compliance Manufacturing Production

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