· Responsible for new product development, experiment and optimize buffer composition, reagents and recipes;· Responsible for the testing and experiments of key raw materials, able to independently plan, analyze and summarize experimental data;· Responsible for solving technical problems encountered during the research, development & production process;· Strictly comply with laboratory-related operation and quality management requirements· Collaborate with cross-functional teams to meet projects goals with overall organizational objectives.· Any other ad-hoc duties or projects as required by the management team.Requirements· Experience in IVD, clean environment production, quality system, R&D and etc;· Expertise in the operation and maintenance of lab instruments and data systems;· Understand the relevant requirements of the production quality system for in vitro diagnostic products;· A bachelor's degree with 7 years of relevant experience, a master's degree with 3 years of relevant experience, or a doctorate degree with at least 1 year of relevant experience. Others are welcome to apply.· Familiar with in vitro diagnostic products such as ELISA, lateral flow immunoassay, biochemistry, PCR, Immunoassay etc;· Familiar with IVD product development and commercialization life cycle;· Systematical project management, good planning, execution and timely communication. Good presentation skills.· Majoring in biology, medicine, laboratory science, immunology, pharmacy or quality engineering are preferred;· Enthusiastic, proactive, and down-to-earth work attitude, strong communication & execution ability, results driven, and a team player;· Meticulous and strong sense of responsibility; able to handle stress and tight schedule;· Please send a comprehensive resume, a cover letter, along with your current and expected salary and a recent photograph, to .· We regret that only shortlisted candidates will be contacted; To receive updates for future opportunities, please follow my LinkedIn page:
