CCP Trainee at Lonza
Tuas, , Singapore -
Full Time


Start Date

Immediate

Expiry Date

08 Nov, 25

Salary

0.0

Posted On

09 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Electrical/Electronic Manufacturing

Description

Lonza is the pioneer and world leader in the CDMO industry operating across 5 continents, setting the pace with cutting-edge science, smart technology and lean manufacturing. We turn our customers’ break-through innovations into viable therapies and manufacture the medicines of tomorrow. At the heart of every scientific breakthrough are talented individuals collaborating to develop solutions that empower businesses to improve lives. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. As a Biotechnologist at Lonza Mammalian business, you’ll be part of our globally recognized network, driving the production of mammalian cell culture and treatments.
Join our best-in-class high performance Integrated Biologics team at our Tuas site in Singapore to gain unparalleled exposure to cutting-edge biotechnology and innovation, and make a difference from day one. Learn new skills and capabilities, and grow your career with us in manufacturing therapeutic proteins under cGMP conditions. Find out more about what a life at Lonza in Singapore could look like for you by watching this short video.

Responsibilities
  • Execute daily routine and repair work orders as assigned.
  • Ensure all routine maintenance works are duly carried out as scheduled and in compliance with Engineering standards and procedures.
  • Respond on-call for maintenance/service breakdown and support ongoing operations.
  • Troubleshoot equipment breakdowns and carry out basic repairs or report back to Supervisor.
  • Supervise vendors/service providers activities for daily routine HVAC and maintenance work to ensure equipment is maintained in full operational status.
  • Work with supervisor to manage site HVAC system.
  • Perform regular equipment inspections to feedback on HVAC status. Execute/supervise repairs/upgrading works to enable smooth handover and minimize disruption to production schedule.
  • Apply and close work permits with Area/System Owners for vendor/service providers.
  • Work with Supervisor to maintain all site HVAC in optimum condition in compliance with Good Manufacturing Practice (GMP) & EHS requirements. Ensure all GMP documentation related to maintenance activities is completed accurately and processed to full completion.
  • Communicate to Supervisor/Manager when encounter non-compliance issues including work delay, breakdown, missing parts etc.
  • Carry out any other duties and responsibilities as assigned by Supervisor/Manager, including but not limited to the above.
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