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General Electric Lead Operater in Shanghai, China

Job Description Summary

Perform the daily operations of plants to ensure reliability and consistency on the production line. Includes Service Shops. Accountable for the quality of own work. Subject to direct operations supervision/prescribed work instructions/systems checking. Executes within a well-defined operations framework. There is generally a step by step sequence of standard operational tasks which need to be followed to achieve an end result.

GE Healthcare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.

Job Description



  • Maintain a safe place of work for his/her responsible area.

  • Monitor Production Operators performance and identify training needs.

  • Ensure staff has been trained appropriately before enrolling the job and the qualification matrix is up to date accordingly.

  • Train the new staff in the area and fill the training record.

  • In conjunction with supervisor, organize operator’s area allocation, overtime and shift when so required.

2. Production

  • Monitor line performance; achieve daily/weekly production targets.

  • Assist shift supervisor to complete departmental goal setting and monitoring the progress by OEEs figures.

  • Participate in the process if necessary.

  • Carry out trend registration in the area and solve the technical problem during production.

  • Input the process data into SAP system within agreed time.

  • Identify and replenish the consumable requirements within his/her own area.

  • Maintain a high level of housekeeping and paperwork standards in adherence with cGMP and GEHC SOPs.

  • Check and review the documentation (batch records, logbooks) is filled in accordance with regulatory requirements.

3. Quality management

  • Be fully trained and competent in cGMP requirements that applicable to his/her responsible area.

  • Assist supervisor to ensure that all documents in their area are current, accurate and comply with cGMP.

  • Area responsible person for control of batch documentation: organizes production arrangements, archiving and retrieval when necessary.

  • Be responsible for deviation and corrective actions following up and implementation.

  • Aim and work in order to eliminate deviations within his/her area.

  • Participate IPC testing.


  • Minimum college or university education and minum2 years experience in the Pharmaceutical/Chemical/food Industry is preferred.

  • Supervisory/team leader experience would be an asset but training will be provided.

  • Good knowledge in English and computer is required.

Inclusion and Diversity

GE Healthcare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.


Additional Information

Relocation Assistance Provided: No