Latest Biotechnology Intern Opportunities at Lonza – BS Graduates Apply for the Intern Position
Join Lonza, a global leader in life sciences, as a Manufacturing Intern and gain hands-on experience in therapeutic protein production under cGMP conditions. This role offers exposure to cutting-edge biologics manufacturing, industry-leading technology platforms, and collaboration with biotech innovators, all while being part of a team making a meaningful difference in global healthcare.
- Job Posting: Biotechnologist Intern
- Job ID: R67985
About Lonza
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.
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.
Job Description
The Manufacturing Intern role at Lonza is responsible for supporting therapeutic protein manufacturing under cGMP conditions. This individual works in a clean room environment within a team led by a Section Lead. The Intern will be assigned to a specific operational area (Small Scale, Large Scale, Centralized Operations) with a focus on Upstream, Downstream, Solution Preparation, or Production Support functions.
Primary Responsibilities
- Learns and performs well-defined procedures
- Attains a basic understanding of cGMPs and compliance in a GMP manufacturing setting
- Performs basic laboratory tasks (pH and conductivity measurement, water sampling, etc.)
- Ensures manufacturing supplies and batch records are readily available for the next 24 hours of production activities
- Applies and upkeeps 6S concept and housekeeping in MFG suites
Requirements
Currently enrolled in ITE/Diploma/Degree in a relevant science discipline (Biotechnology, Pharmaceutical Science, Chemical Engineering, Chemistry, Biochemistry or Biology)
Working Hours
12 hr day shift work (0800hrs – 2000hrs) with 2 weeks repeating pattern
Supervision Received
- Daily supervision of routine work and detailed instructions on new assignments
- Documentation of tasks performed when required
- Basic decision-making involves knowing when to seek help and who to contact
- Coaching on the manufacturing process flow
Other Departmental Duties
Instruction may be provided by co-workers, supervisors, or cross-departmental representatives to facilitate continued production within GMP, with the consent of the immediate Supervisor.
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