Biotechnologist 2/3
1 month ago
At Lonza, we are seeking a highly skilled Biotechnologist 2/3 to join our Manufacturing Team at our Tuas site in Singapore. As a Biotechnologist 2/3, you will be responsible for the manufacturing of therapeutic proteins under cGMP conditions.
Key Responsibilities:- Learn and perform well-defined procedures within a GMP manufacturing setting
- Perform equipment monitoring & basic 6S housekeeping
- Perform basic laboratory tasks (e.g. sampling, pH/ conductivity/ osmolality measurements etc.)
- Perform routine sanitization tasks to maintain facility standards
- Trained & signed off on Performance Measures (PMs) relating to CIP/ SIP/ basic tank & instrument operations
- Demonstrate aseptic technique in the handling of product/ materials
- Perform basic process & equipment troubleshooting
- Multi-task on equipment preparations & operations to ensure adherence to schedule
- Attain full competency in the performance of all operations relevant to manufacturing areas assigned.
- Display basic process & equipment troubleshooting ability under routine scenarios.
- Become a technical process expert by exhibiting basic understanding of critical process/operational parameters and target/acceptable ranges, as well as interactions between different process parameters.
- Use Standard Operating Procedures (SOPs), logbooks & Batch Records (BRs) effectively & competently
- Submit samples via Laboratory Information Management System (LIMS)
- Skill and knowledge of aseptic technique for subculture stages example using culture flask, spinners, wave bioreactors, etc.
- Technical knowledge on the bioreactor culture control example pH/DO control, CO2/O2 control, cell performance, and metabolites analysis.
- Skill and knowledge of column chromatography techniques, tangential flow filtration techniques, micro/Nano filtration techniques, pH/Conductivity adjustment techniques, aseptic techniques.
- Technical knowledge on the chromatography operating interface example using UNICORN software and various DeltaV control parameters for chromatography and UF operation.
- Knowledge in single use applications for the respective processes.
- Degree/Diploma in a related Science/Engineering discipline
- Some relevant work experience in a similar manufacturing industry or cleanroom environment
- Knowledge of Biopharmaceutical processing is an added asset
- Knowledge of cGMP applications
- Positive team oriented attitude
- Strong communication and interpersonal skills
- Willing to perform rotating 12-hour shift pattern
At Lonza, we are committed to improving lives all around the world. We offer a dynamic and challenging work environment where you can grow and develop your skills. If you are a motivated and detail-oriented individual who is passionate about biotechnology, we encourage you to apply for this exciting opportunity.
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