- Preferably PhD in immunotoxicology, immunology or equivalent degree, with 1 to 2 years of industry related experience.
- Experience and knowledge of various cytokine analysis platforms (e.g. Luminex, ELISpot and ELISA, etc.).
- An in depth understanding of GLP/GCP and regulatory guidelines.
- Skilled in conducting research, compiling data, data interpretation, and writing reports according to FDA, EMA and NMPA regulatory requirements.
- Proven track record of method development and troubleshooting using de-novo approaches or transfer of qualified/validated method.
- Effective oral and written communication skills.
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