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    Formulation PET Lead - Taizhou, 中国 - AstraZeneca

    AstraZeneca
    AstraZeneca Taizhou, 中国

    4天前

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    全职
    描述
    Join us as a PET Lead- Formulation, a strategic leader responsible for the overall performance of a Process Execution Team (PET). This role is a unique opportunity to set strategic and tactical direction for the PET, ensuring alignment with high-level Site and Product Supply business objectives. As a PET Lead, you will be driving alignment for the team to flow materials & information through the value stream in a continuous improvement environment.

    Responsibilities

  • Manage all production activity and people development in department to secure on time delivery of quality products.
  • Acting as supply chain function leader to implement the related strategies, policies and programs to drive for overall on-time delivery, good quality and cost performance.
  • Evaluating the feasibility & viability of introducing new products and leading the technical transfer of any such products into Taizhou site.
  • Leading the routine establishment & validation activities of current Product and Process at Taizhou site relating to excipient, API or component related changes.
  • Lead the Formulation technical team responsible for delivery of Product security and anti counterfeit.
  • Leading the development of new products in partnership with relevant Contract Research Organizations.
  • Proactively generating product / process Improvement initiatives (Inc Statistical Analysis) to drive the delivery of the PET KPI's. This relates to the Formulation and Packaging PET's.

    • Tasks:

  • Production Management
  • Supply Chain Management
  • Project Management
  • Compliant site validation status
  • Responsibility for
  • GMP/Compliance/SHE

    • Requirements:

  • Bachelor degree in pharmaceutical or relevant specialties or intermediate professional technique certificate or registered pharmacist license
  • At least 3 years practical experience in pharmaceutical production and quality management during which at least 1 year in management position in production
  • ≥ 7 years relevant work experience in a multi-national pharmaceutical industry
  • Familiar with pharmaceutical production management related laws, regulations and rules and regulations
  • Excellent written and oral English proficiency

    • Master the following skills:

  • Reporting skill
  • Pharmaceutical knowledge; including production and regulatory processes
  • GMP知识GMP knowledge
  • Knowledge of process validation requirements
  • Project management
  • Knowledge of technology transfer / NPI procedures
  • Knowledge of AZ Project management (PMF) tool
  • Knowledge and experience of AZ risk management (IRM) process
  • Demonstrated ability to effectively lead change at multiple levels in an organization

    • Date Posted

    11-3月-2024

    Closing Date

    29-4月-2024
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