跳到主要内容
搜索

Formulation PET Lead

地点 泰州市, 江苏, 中国 职位 ID R-194335 发布日期 04/30/2024
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


AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

Glassdoor logo Rated four stars on Glassdoor

优秀的文化,出色的工作任务,充满支持的管理模式。 公司内部的轮换机会。 他们重视包容性和多样性。