该职位来源于猎聘 Role Description: Work with key business users to convert project requirements into an automation strategy/requirements and technical solution.

Define core Automation and IT integration requirements on projects into User Requirement Documents: communicating these requirements to vendors and ensuring that systems are specified and delivered in alignment with the automation strategy (contract management not part of this role). Provide design assurance reporting and technical feedback during capital project design - from concept through detailed design and equipment selection (Including where necessary, detailed design document reviews and sign off). Support Project Technical Manager and Work Package Owners during all phases of project in technical issue management and governance to ensure a compliant technical solution to quality and safety.

Support C&Q On Testing And Qualification Activities (Including Where Necessary, Document Generation And Test Participation). Support The Work Package Owner To Proactively Plan The Work Ahead. Experience

Minimum of 5 years of experience in automation system engineering within the pharmaceutical industry.

Proven experience in managing and executing automation projects in a global setting, particularly in China and/or Europe.

Experience in the full lifecycle of delivering automation systems in a licenced GMP commercial facility (Including the design, specification, procurement, installation, start up and commissioning of automation systems).

Strong knowledge of automation systems, including PLCs (Programmable Logic Controllers), SCADA (Supervisory Control and Data Acquisition), and DCS (Distributed Control Systems).

Experience with automation software and tools such as Siemens, Rockwell, or Emerson.

Familiarity with industry guidelines, standards and regulations, including GAMP, GMP, FDA, and EU regulations.