Malaysians are welcome to apply
Job Responsibilities:
- 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:
- Diploma in biomedical science/biotechnology or related discipline. Degree holders will also be considered.
- 1 – 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/or internship will also be considered.
- Expertise in cell culture.
- Experience in cell/gene therapy preferred.
- Good knowledge in GMP and other relevant guidelines preferred.
- Self-Initiated, able to work independently and in a team.
- Good communication and interpersonal skills.
Career Level
- Junior – Mid level Executive
