Today, Lonza is a global leader in life sciences operating across five 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.
As a Biotechnologist at Lonza Cell & Gene Therapy business, you’ll be part of our globally recognized network, driving the production of cell & gene 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. Learn new skills and capabilities. Grow your career with us in manufacturing therapeutic proteins under cGMP conditions.
The Cell and Gene Therapy (CGT) Manufacturing Intern role is responsible for the support of CGT manufacturing under cGMP conditions. This individual works within the clean room environment in a team led by a Section Lead. The Intern will be assigned to a various operational area, such as Manufacturing or Planning/Production Support function.

Working hours:

• Either office hours or 12 hr shift work (0800hrs – 2000hrs) with 2 weeks repeating pattern.

Primary Responsibilities

• Learns and performs well-defined procedures.
• Attain a basic understanding of cGMP’s and compliance in a GMP manufacturing setting performing both supervised and unsupervised tasks.
• Perform basic laboratory tasks (pH and conductivity measurement, water sampling, etc)
• Perform routine sanitation tasks to maintain facility standards.
• Ensuring manufacturing supplies and batch records are readily available for next 24 hours production activities.
• Apply and upkeep 6S concept and housekeeping in MFG suites

Other Departmental Duties

• Instruction may be provided by co-workers, supervisors, or cross-departmental representative to facilitate continued production within GMP, with the consent of the immediate Supervisor.

Supervision Received

• Daily supervision on routine work and detailed instructions on new assignments, including organizing and planning of tasks to ensure timely completion.
• Documentation of task performed when required.
• Basic decision making, knows when to seek help and who to contact.
• Coaching on manufacturing process flow.

Requirement

• Degree in relevant science discipline (Biotechnology, Pharmaceutical Science, Chemical Engineering, Chemistry, Biochemistry or Biology)

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 happiness that comes with improving lives all around the world. The happiness that comes with making a meaningful difference

Primary Responsibilities

• Learns and performs well-defined procedures.
• Attain a basic understanding of cGMP’s and compliance in a GMP manufacturing setting performing both supervised and unsupervised tasks.
• Perform basic laboratory tasks (pH and conductivity measurement, water sampling, etc)
• Perform routine sanitation tasks to maintain facility standards.
• Ensuring manufacturing supplies and batch records are readily available for next 24 hours production activities.
• Apply and upkeep 6S concept and housekeeping in MFG suite

Other Departmental Duties

• Instruction may be provided by co-workers, supervisors, or cross-departmental representative to facilitate continued production within GMP, with the consent of the immediate Supervisor