Perform well-defined procedures in cGMP manufacturing and R&D settings.
Demonstrate aseptic technique in the handling of product / materials and participate in aseptic process simulations.
Able to multi-task e.g. con-currently involved in cGMP manufacturing and/or validation tasks and/or R&D trial.
Able to use Standard Operating procedure (SOPs), logbooks and Batch Manufacturing Records (BMR) effectively and competently.
Assist in process development e.g. creating scalable processes with improved product yield and reduced production costs.
Any other tasks / projects assigned by superior and management.
Job Requirements:
Degree/Diploma in biomedical science/biotechnology or related discipline.
Minimum 1 \xe2\x80\x93 3 years working experience in similar manufacturing industry or cleanroom environment. Fresh graduates with hands-on experience in cell culture during their final year project and internship will also be considered.
Expertise in cell culture.
Experience in cell/gene therapy preferred.
Good knowledge in GMP and other relevant guidelines.
Self-Initiated, able to work independently and in a team.
Good communication and interpersonal skills.
Flexible to adjust personal schedule to support GMP manufacturing and R&D trial runs.
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