Manufacturing Engineer - Cleaning

Johnson & Johnson Innovative Medicine

Suzhou, Jiangsu, China
Not specified (assumed hybrid or onsite based on job nature)
Manufacturing cleaning process development
Process validation and compliance
Sap system process routing maintenance
Johnson & Johnson Innovative Medicine is seeking a Manufacturing Engineer specializing in cleaning processes to join their team in Suzhou, China. The role involves collaboration with cross-functional teams to develop and maintain cleaning procedures, support manufacturing start-ups, and drive continuous improvement initiatives

Job Summary

  • At Johnson & Johnson, we believe health is everything and strive to innovate across healthcare solutions to deliver breakthroughs that profoundly impact health for humanity.
  • The role involves full responsibility for cleaning process related audits and requires collaboration with multiple departments to ensure compliant and efficient manufacturing start-up and operations.
  • The Manufacturing Engineer will lead or participate in continuous improvement projects aimed at improving quality, cost, delivery, and efficiency while supporting capacity planning and quality system development.

Matching Summary

Match Score: 85

Johnson & Johnson Innovative Medicine is seeking a Manufacturing Engineer specializing in cleaning processes to join their team in Suzhou, China. The role involves collaboration with cross-functional teams to develop and maintain cleaning procedures, support manufacturing start-ups, and drive continuous improvement initiatives.

Skills & Requirements

Must-have

  • Manufacturing cleaning process development
  • Process validation and compliance
  • SAP system process routing maintenance
  • Cross-functional collaboration
  • Continuous improvement initiatives
  • Equipment maintenance and calibration
  • Quality system implementation

Nice-to-have

  • Financial knowledge for budget identification
  • Capacity planning and layout design
  • Training delivery for shopfloor employees
  • Understanding of FDA QSRs and ISO 9000
  • Computer software validation requirements
  • Health, Safety and Environment program participation

Key Requirements

  • Understanding of FDA QSRs, ISO 9000, CFDA requirements
  • Experience with process validation and equipment qualification
  • Financial knowledge for capital spend and budgeting
  • Ability to deliver training to employees
  • Experience in manufacturing process documentation
  • Knowledge of computer software validation

Work Rights

Not specified

Tailored Resume

Cover Letter