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.

We are currently looking for a CCP Trainee who can commit with us for 15 months to join the engineering team.

**Responsibilities**:

- Complete the approved projects listed in the CAPEX plan and capital expenses within the total approved budget.
- Together with the users, define the project scope. Drive the feasibility study, concept design, basic design, detailed design phases and a +/- 10% budget of approved projects.
- Manage the contractor during the construction phase to deliver the agreed quality, costs and schedule of the projects.
- Coordinate and manage the commissioning, IQ and OQ phases of the projects. Ensure completed projects and documents/drawings are properly handed over the users and Maintenance. Ensure project close out process is completed.
- Propose and evaluate modifications to equipment, processes and operations to improve safety, increase efficiency and enhance company goals.
- Supervise outside contractors to develop and implement Capital projects and plant modification.
- Support customer queries on process related issues.
- Involve in new customer tech transfer and risk assessment
- Good knowledge of key business process such as change control, permit to work, drawing management, documentation etc.
- Support the team on inspection readiness at all time.
- Any other duties as assigned by your Supervisor/Manager

Requirement:

- Degree in a relevant Science field or equivalent
- 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.