Maintenance Engineer

2 weeks ago


Qingdao, Shandong, China AstraZeneca Full time

Summary

This position is located in Qingdao. During the project phase, you will be involved in the design, construction, commissioning, and qualification of the Qingdao pMDI factory as the end-user to better support the project team. The aim is to ensure knowledge and experience are standardized and improved to support future commercial production through lean standardization and continuous improvement such as SOP/work instructions. It is essential to focus on continuous improvement of processes, equipment, and operations early in the project. You should be proficient in tools like lean, especially TPM, and emphasize communication with internal and external stakeholders.

As the project transitions to commercial production, your role will involve executing maintenance plans properly and efficiently under safety and GMP compliance, responding quickly to on-site repair needs, and ensuring all production equipment operates safely and efficiently to support the core business processes of the pMDI factory. Additionally, you need to enhance technical competencies and maintain effective communication with internal and external stakeholders regarding equipment issues.

Responsibilities

  • Fully engage in various project phases and provide valuable insights as an end-user.
  • Apply best practices from other sites and industries to the Qingdao project.
  • Ensure standardization and continuous improvement from project to commercial production readiness.
  • Demonstrate strong problem-solving and continuous improvement skills to ensure project success.

Production Equipment Maintenance

  • Responsible for maintaining dispensing, formulation, and filling equipment and software management.
  • Promptly address equipment failures during production.
  • Submit maintenance system update recommendations based on field experience.
  • Order equipment spare parts timely to meet production needs.

Equipment Modification and Improvement

  • Modify defective dispensing, formulation, and filling equipment and software to enhance performance.
  • Draft verification documents for equipment upgrades and modifications.
  • Provide suggestions for optimizing operation procedures.

Equipment Operation and Validation Support

  • Operate relevant equipment during production batches when required.
  • Act as a super user for equipment service functions during maintenance or repairs.
  • Support validation and revalidation activities.

GMP/Compliance/SHE Responsibilities

  • Adhere strictly to company GMP/SHE/compliance policies and standards related to the position.
  • Collaborate effectively with team members in daily operations.

Requirements

  • Bachelor's degree or higher in an engineering field.
  • Knowledge of mechanical, electrical, electronic, and industrial automation.
  • Proficient in reading and speaking English.
  • Minimum of 5 years of production equipment maintenance experience in a multinational pharmaceutical company.
  • Experience in project or new site startup.
  • Ability in process control system software programming, debugging, troubleshooting, and strong communication skills.
  • Familiarity with dispensing, formulation, filling process equipment, and technical solutions.
  • Knowledge of mainstream DCS/PLC programming software and batch production execution.
  • Proficiency in Profibus-net/DP, Modbus, and FF communication protocols.
  • Understanding of the basic working principles of various sensors in automatic control systems.

Date Posted

23-May-2024

Closing Date

29-September-2024



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