CCP6 Trainee, QC

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Singapore
In-Office
Pharmaceutical
At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization.
The Role

 

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.

The trainee we are looking for will join the CCP training program in the Quality Control team at Singapore Tuas site.

What you'll do:

  • To prioritize and perform the various testing/analysis in timely manner, in order to support the business requirements.
  • Analysis of final product, in-process, stability samples according to Standard Operating Procedures and Test Methods.
  • Documentation and review of results in accordance with current Good Manufacturing Practices (cGMP).
  • General lab support including housekeeping, equipment maintenance, inventory of supplies, lab supplies ordering, management of glass wares, autoclaving etc.
  • Prepare, maintain standards and reagents as required by GMP documents.
  • Responsible to follow data integrity requirements.
  • Actively contributes to operational efficiency/continuous improvement initiatives.
  • Any other duties as assigned by your Manager.
  • Uphold data integrity principle in accordance to Lonza policies.
  • Proactively evaluate, identify and improve data integrity process

What we're looking for:

  • Degree in a relevant Science field or equivalent
  • Individual without prior working experience in the biopharmaceutical manufacturing industry may also apply
  • Understanding of the application of mammalian cell culture for the production of biopharmaceuticals
  • 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.

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The Company
HQ: Basel
0 Employees
Year Founded: 1897

What We Do

At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization. Our community of 16,000 talented employees work across a global network of more than 30 sites to deliver for our customers across the pharma, biotech and nutrition markets.

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