Process Engineer

Basic qualifications:

Education (minimum/desirable)教育: Bachelor Degree (Biological/or technical profile)

Minimum Education:最低教育: Bachelor Degree

Desired Education: 有以下教育经验更佳: Master Degree (Biological/or technical profile)


Spoken 口语 / Written书写 / Read阅读

English英语 良好 fluent 良好 fluent 良好 fluent

Chinese中文 优秀 excellent 优秀 excellent 优秀 excellent


Minimum 最低要求 : +5 year's experience in high quality healthcare international regulated industrial environment and in best manufacturing practices GMP.

Preferred qualifications:

Desired 有以下经验更佳:

  • Experience in sterile manufacturing including formulation, filling, freezer etc.,
  • Experience in technical support technology, such as washing & sterilization, CIP/SIP system
  • Knowledge of GSK GQP and GQMP, Well understanding of cGMP
  • Aware any project risk and necessary mitigation plan
  • Good communication skill

Skills (e.g. IT)) 工作技能 (如IT技能等) :

  • Good knowledge of operating experience of pharmaceuticals plants.
  • Good knowledge of cross functional business processes
  • Management knowledge establishing strong working relationships with customers and in-depth understanding of their operations and process requirements
  • Computer literate, MS office, CAD, MS Project
  • Flexibility in terms of working hours and travel
  • Self-motivated approach to responsibility and ownership
  • Ability to maintain deliverables by communication
  • Capability to maximize team performance
  • Strong analytical skills to identify the real issues quickly and to prioritise appropriately


Job Purpose:

The employee is allocated to one or more projects as Process Engineer located in GSK Tian Yuan site. He/she shall be responsible for development engineering solution and URS of the process equipment /facilities for site GMP remediation project to ensure the project continuity according to GSK standards and other requirements form company.

Major Accountabilities:

Engineering Design

  • Manage all process technology aspects of GSK TY vaccine engineering, being responsible for process engineering technology. Acts as an engineering technical lead on process engineering, implements local and global expert-inputs in a timely fashion with high quality.
  • Possesses excellent process design knowledge, is responsible for process equipment readiness including related automation of the entire facility within given budget, time and quality aspects.
  • Develops reliable and flexible process equipment concepts, summary as key inputs for URS preparation.
  • Leads and coordinates process sub teams and the engineering partners on process topics
  • Coordinate with global discipline SME on technical issue clarification and follow up with accurate remediation solutions
  • Advise and review all relevant technical documents for the project and work for the successful completion of the project and co-ordinate with other specialists.
  • Maintain good record on change management for project planning phase
  • Maintain a comprehensive filing system to provide a current basis for all documents, decisions, disposition of directives and inquiries and information exchanged among the parties, including agreements and modifications.


  • Participate into procurement activities from technical point of view to evaluate the best offers for project, including RfQ documents preparation, bidding evaluation and clarification, contract & PR/PO preparation.
  • Provide the PM with updated information regarding the status of procurement works, especially for the long lead items.


  • Coordinate the CD/BD Program within process discipline, checking and reporting the actual onsite execution progress
  • Dealing with all contractors in planning, project time control and quality control.
  • Review, track and supervise any changes during execution phase.
  • In addition, responsible for developing commissioning plan and managing commissioning.
  • At the end, monitor all the changes reflected in the Contractor's "As-Built" drawings, support PM on project handover process.


  • Coordinate and supervise all FAT/SAT/DQ/IQ/OQ works with contractors, engineering team and validation team
  • Prepare all necessary documentations to complete the validation works


  • Attend technical meetings and advise the Project Manager on procedures and requirements.
  • Daily organisation of project running and technical filing.
  • Coordinate with internal consultancy to ensure compliance with Corporate requirements
  • Coordination of technical requirements between the PM Team, global engineering and Consultants
  • Coordination with GSK internal Departments especially Sourcing/legal/Engineering/QA& QC
  • Other tasks assigned by supervision managers related to Process discipline

Key Performance Indicators:

  • Ensure GSK engineering standard fully implemented during each project execution phases
  • Support project manager to control project budget spending within +/- 10 %
  • Support project manager to control project milestones delivery time according to schedule
  • CAPA closure 80% on rate or greater
  • HSE review for all projects and zero lost time for accident and recordable at <=X%

Job Dimensions:

Number of associates下属人数:NA

Financial responsibility财务职责:N/A

(Budget预算, Cost成本, Sales销售, etc.)N/A

Key business partner主要工作联络部门: 制造事业部(Production)、QA、QC、Val、环境安全健康(EHS)

Contact information:

You may apply for this position online by selecting the Apply now button.

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