Job Description
- Develop, validate and perform bioassays and bioanalytical assays in compliance with FDA/EMA and GLP guidelines
- Refine current method in response to changing requirements of drug development
- Prepare study plan and study data of assays performed
- Analyse and present data/results
- Document work, results, analyses and findings in laboratory notebooks or study folders as appropriate according to workflow
- Draft SOPs and study reports
- Perform literature review for various drug pipelines and assays as required
- Meet project milestones with set quality
- Ensure scientific integrity of studies conducted and reports submitted
Requirements
- BSc or MSc in biomedical science, life science or equivalent
- Prior research and development experience are required
- Proficient in mammalian cell culture and aseptic techniques is a must
- Experience in ligand binding assays mainly ELISA, cell-based assays, SDS-PAGE, western blot and reporter assays is highly desirable
- Good knowledge of cell based (potency) or ligand binding assays required in drug development process
- Proficient with office software (MS office, Teams), and familiar with statistical tools (Graphpad Prism, XLSTAT or PLA)
- Knowledge of bioassays, bioanalytics and its method validation, GLP and ISO17025 is a plus
- Good written and verbal communication skills
- Superior problem solving and troubleshooting skills, attention to details
- Good interpersonal skills
