Ccp Trainee

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.

**What you’ll do**:

- 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.
- 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.

**What We’re Looking for**
- Degree in a relevant Science field or equivalent
- Fresh graduates are welcome
- Individual without prior working experience in the biopharmaceutical manufacturing industry may also apply
- Understanding of cGMP regulations
- Good problem solving and anlytical skills
- Good communication and teamwork skills

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.