Biotechnologist, CGT

Roles & Responsibilities

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. 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.

Did you know that we are the 1st biologics contract manufacturer in Singapore? We offer you exposure to upcoming biotech and established pharmaceutical companies and to the manufacturing technology needed to produce mammalian treatments and cell therapies of tomorrow. Our global manufacturing network is recognized for its reliable, high-quality services, regulatory track record, global footprint, innovative technology platforms and extensive experience – we, in Singapore are proud to be part of this global network.

As our Cell & Gene Technologies (CGT) business grows, we are looking to further strengthen our manufacturing team in Tuas, Singapore. The Biotechnologist is responsible for the manufacturing of cell therapy products and media in accordance to cGMP regulations.

The role requires flexibility to be able to work in a 12-hour rotating (day, night and weekend) shift. Willing to work in cleanroom environment requiring the removal of jewelry/ makeup, donning of over suits/ coveralls, safety shoes, hair cover, gloves and safety glasses/ goggles.

Job Description

• Attains a thorough understanding of the principles of cGMP compliance and clean room practices
• Executes batch records, ensuring right-first time and accurate documentation
• Maintains training status to perform required GMP tasks
• Performs environmental monitoring during production
• Performs suite support activities, e.g. equipment cleaning, housekeeping and escalates non-routine situations (e.g. deviations, equipment alarms) per site procedure
• Use electronic systems to perform work (e.g. document management system (DMS), Lab Information Management System (LIMS), Trackwise)
• Reviews executed batch records and logbooks in an accurate and timely manner
• Suggests and participates in continuous improvement initiatives.
• Gains thorough understanding of critical process parameters and operational parameters
• Inputs into investigation of complex technical problems, compliance failures, performs process & equipment troubleshooting and Lab in charge responsibility

Key requirements:

• Diploma / Degree in Science disciplines or working experience in biopharmaceutical industry or cleanroom environment
• Knowledge of cell culture and the principles of aseptic processing within a classified environment is not essential, but an advantage
• Strong team-oriented work ethic
• Planning, Organizing, & Controlling
• Willing to perform rotating 12-hour shift pattern

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.

Tell employers what skills you have

Document Management
Aseptic Processing
Cell
Troubleshooting
cGMP Manufacturing
GMP environment
Investigation
Cell Culture
Production
Biologics
Pharmaceuticals
Life Sciences
c-GMP
Manufacturing
Lab production
Cell Therapy

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