GMP Maintenance Engineer (12h Shifts) – Onsite Tuas

Lonza

Singapore

Presencial

Confidential

Jornada completa

14 días+

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

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Ventajas ofrecidas por este puesto de trabajo

Agile culture
Inclusive workplace
Competitive compensation
Medical insurance
Bus to Tuas site

Descripción de la vacante

Lonza Singapore operates a fully site-based Tuas facility. The Associate Engineer will perform 12-hour rotating day and night shifts, collaborating in person to ensure high precision in medicines manufacturing. You’ll gain exposure to SOPs, GMP documentation, and maintenance of production equipment.

The role emphasizes safety, teamwork, and adherence to Lonza rules, with opportunities for development within a global healthcare environment at a leading life sciences company.

Formación

  • Diploma or degree in engineering (mechanical) is required.
  • GMP experience is preferred.
  • Ability to work rotating day and night shifts.
  • Strong communication and stakeholder management skills.

Responsabilidades

  • Operate SAP to perform transactions.
  • Execute routine and repair work orders as directed by Engineer/Supervisor.
  • Ensure maintenance work is performed per schedule.
  • Maintain GMP documentation accurately and fully.
  • Read PID and equipment drawings to identify components.
  • Perform Job Safety Analysis and Risk Assessments, Fall Protection, Working at Height.
  • Be on shift or available on-call to support operations and maintenance calls.
  • Complete other duties as assigned by Engineer, Supervisor or Manager.

Conocimientos

GMP experience
Communication skills
Shift work

Educación

Mechanical engineering (Diploma/Bachelor)

Herramientas

SAP

Descripción del empleo

Lonza Singapore operates a fully site-based Tuas facility. The Associate Engineer will perform 12-hour rotating day and night shifts, collaborating in person to ensure high precision in medicines manufacturing. You’ll gain exposure to SOPs, GMP documentation, and maintenance of production equipment.

The role emphasizes safety, teamwork, and adherence to Lonza rules, with opportunities for development within a global healthcare environment at a leading life sciences company.

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