Key Role:

• Involve in the setup and maintenance of a genomic laboratory according to GLP standard guideline
• Conducts and directs assays and procedures according to and in compliance with standard ISO.
• Assist with designs experimental plans, leads study execution, analyse experimental data, write technical reports, quantitative analyses, and quality report summaries for vaccine projects.
• Participate in development and execution of Quality Assurance and Quality Control procedures for vaccine.
• Conduct key scientific research for development of novel infectious disease vaccine and interpret experimental data to determine follow-up activities.
• Conduct lab procedures in virus handling/infectivity techniques including virus Inactivation, Ribonucleic Acid Isolation, Polymerise Chain Reaction (qPCR) and perform and report  technical work in containment laboratory (BSL-2).
• Maintain a current understanding of relevant literature and scientific advances relevant to specific projects.
• Perform documentation related to purchasing activities including PR, DO, Invoice.
• In-charge of inventory for chemical, consumable and equipment for AmVap project

Requirements:

• Master in Biological Sciences, Cancer Research, Molecular/Cell Biology, Biotechnology, Medical Science with 3 years of experience in post-graduate research and / industry.
• Having experience and scientific knowledge in microbiology, virology, Gene expression profiling, microRNA and signalling pathways is required
• Experience with molecular biology technique
• Fluent spoken and written English and Strong communication and teamwork skills are essential as the candidate is expected to interact with international collaborations.
• Ability to work in a high paced inter-disciplinary and capable of performing work on off shifts.
• Advanced computer skills and statistical analyse