Shanghai pinnaclesdx Medical Technology Co., Ltd.

1. Based on project requirements, build the software system framework and conduct module requirement analysis, and develop a software requirement specification document;
2. Independently complete the code writing of functional modules, including hardware interface implementation, software interface, functional module settings, work mode management, etc., and conduct module functional unit testing according to specifications;
3. Responsible for the design and development of application layer software for embedded Linux platforms;
4. Collaborate with other departments of the project team to conduct system performance indicator testing;
5. Responsible for writing software technical documentation, conducting functional testing, and improving maintenance;
6. Work closely with other departments in the project team to provide continuous and reliable support.

1. Bachelor's degree or above in computer or software related majors; More than 2 years of experience in embedded Linux development;
2. Proficient in C/C++, with a deep understanding of object-oriented programming, comprehensive software knowledge architecture, solid foundation, and proficiency in commonly used data structures, algorithms, and design patterns;
3. Familiar with embedded Linux related development, debugging, and optimization tools;  
4. Proficient in UML language is preferred;
5. Qt development experience in the medical device industry is preferred, and developers with chemiluminescence instruments are preferred;
6. Priority given to those who have participated in large-scale software development;
7. Possess good learning ability, communication skills, and teamwork spirit;
8. Possess professional dedication, proactive work attitude, and strong sense of responsibility.

1. Quality system construction and maintenance
-Establish and improve the company's quality management system in accordance with relevant regulations and standards such as ISO 13485.
-Regularly evaluate the effectiveness of the quality system, develop and implement improvement plans.
2. Quality standard formulation and implementation
-Develop and update product quality standards, inspection procedures, and operating procedures.
-Ensure that quality standards are strictly enforced throughout the entire production process.
3. Product quality control
-Responsible for quality inspection and monitoring of raw materials, semi-finished products, and finished products.
-Handle non-conforming products, analyze the causes, and implement corrective and preventive measures.
4. Internal Audit and Training
-Organize and implement internal quality audits, track corrective actions identified during audits.
-Carry out quality training activities to enhance employees' quality awareness and skill level.
5. Risk management
-Use risk management tools to assess product quality risks and develop corresponding control measures.
-Timely handle quality complaints and adverse events, and take measures to reduce risks.
6. Regulatory compliance
-Track changes in domestic and international IVD regulations and standards to ensure that the company's products and operations comply with regulatory requirements.
-Assist in product registration and certification work, and prepare relevant quality documents.
7. Data Analysis and Reporting
-Collect and analyze quality data, prepare quality reports, and provide decision support to management.
-Establish a quality indicator system and evaluate quality performance.
8. Cross departmental collaboration
-Work closely with departments such as research and development, production, and procurement to solve quality related issues.
-Participate in new product development projects and provide quality advice and support.

1. Bachelor's degree or above, majoring in biology, medicine, chemistry, pharmacy or related fields;
2. Have at least 8 years of experience in quality management in the IVD industry, familiar with the production process and quality control points of in vitro diagnostic reagents;
3. Familiar with quality management systems such as ISO 13485 and relevant regulatory standards, with the ability to establish, maintain, and audit quality management systems;
4. Strong problem-solving and decision-making abilities, able to quickly respond to quality issues and take effective measures;
5. Strong sense of responsibility, strong communication and coordination skills, and team spirit, effectively leading and motivating team members;
6. Proficient in using quality management tools and statistical analysis methods, such as SPC, FMEA, etc;
7. Good English reading and writing skills, able to read and understand relevant English regulations and standards.

1. Responsible for the sales of the company's inspection product line (including intelligent robots and automated assembly lines for inspection departments), with target end customers including tertiary hospitals, second tier hospitals, third-party medical laboratories, etc;
2. Execute the company's sales plan, complete payment and installation targets on time;
3. Establish and expand sales channels, develop distributors, and be responsible for negotiating and signing marketing contracts within the region;
4. Coordinate and organize product education and related market activities for high-value end customers using direct or semi direct sales models;
5. Maintain relationships with major customers, collaborate with the after-sales service team to provide the best service, and ensure the customer's user experience.

1. Bachelor's degree or above, with over 2 years of sales experience in the medical industry;
2. Sales experience in large-scale inspection equipment such as flow cytometry, mass spectrometry, and assembly lines is preferred;
3. Strong direct sales ability, experienced agents of large IVD enterprises are preferred;
4. Rich hospital and channel resources, especially in the laboratory and equipment departments of tertiary and tertiary hospitals;
5. Excellent sales record, with experience in new product sales, especially 0-1 sales experience is preferred;
6. Good professional ethics, clear logic, strong execution ability, good business negotiation skills and stress resistance.
7. Candidates with experience in laboratory biochemical immune assembly line projects are given priority consideration.