Responsibility:
1, according to the company's development plan and objectives to develop biochemical reagent product research and development plan;
2, new product research and development/transformation project, including feasibility analysis, innovation points and technical routes, key technical problems and process solutions to be solved, expected results and organization of implementation;
3. Develop detailed work plans, experimental schemes and methods, and sort out relevant data in time;
4, timely report the work progress, complete the product development task on time, and pass the acceptance of the results (such as: completion of product registration, innovation project transformation into production, obtain invention patents, etc.);
5, according to the provisions of the company's quality management system for product development and management, preparation of product technical documents, quality standards and registration information;
6. Organize R & D team, guide and arrange experimental personnel to complete experimental work and technical data, review experimental data and technical data, and evaluate work performance;
7, strictly abide by the company's rules and regulations and confidentiality system, and maintain good communication with other departments and relevant personnel;
8. Complete other tasks assigned by leaders.
Requirement:
1. Bachelor degree or above in medical laboratory, clinical medicine, immunology, biotechnology and other related majors;
2, engaged in the research and development of immunodiagnostic reagents for more than 5 years of work experience or have advanced professional and technical qualifications, complete chemiluminescence kit research and development, production and registration experience is preferred;
3, with strong experience in project design, planning and target management, good communication and coordination skills; Able to lead and coordinate the team to complete the development target task;
4, familiar with in vitro diagnostic reagents quality management system, skilled in the preparation of quality management system and product registration requirements of the relevant documents;
5. Good English reading and writing ability and literature retrieval ability;
6, rigorous work, dedication, efficient, can withstand strong work pressure.