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Job requirements

1. Participate in the introduction of new products, establish, maintain and improve SOP and BOM, and verify and confirm key processes, special processes and production equipment。
2. Provide production technical support, be responsible for production exception analysis, process improvement, process optimization, etc., reduce production costs, improve product quality, and fully ensure the achievement of production tasks.
3. Responsible for the analysis of defective products and reworked products, collecting and sorting out defective data, and providing improvement suggestions or programs.
4. Train production personnel on technology and quality.
5. Complete other tasks assigned by the superior leaders on time.

Main responsibilities

1. More than one year of experience in instrument production process, with medical device industry background is preferred, and with optical debugging related work experience is preferred.
2. Have good problem-solving ability, good interdepartmental communication and coordination ability.
3. Have a good work attitude and sense of responsibility, and work actively.

*Send resume to email： zhenzhen.wang@orientgene.com

Job requirements

（一）1. Cooperate with the R&D department to complete the trial production of new products and timely feed back the trial production problems.
（二）2. Be responsible for the commissioning of optical-related processes and the commissioning and testing of the whole instrument.
（三）3. Be responsible for the assembly process with high complexity or difficulty, and guide and monitor the production process to ensure the smooth production.
（四）Assist in the accounting work of receiving, returning and warehousing of production materials.
（五）5. Assist in production safety management and on-site 5S management.
（六）Complete the temporary tasks assigned by the superior leaders.

Main responsibilities

（一）1. Production experience in instruments, household appliances and other industries is preferred, and experience in optical debugging is preferred.
（二）2. Proficient in using common electronic equipment such as multimeter and oscilloscope.
（三）3. Have good problem-solving ability, good communication and coordination ability.

*Send resume to email： zhenzhen.wang@orientgene.com

Job requirements

1. Development of target customers, establishment and maintenance of customer relations;
2. Quote, sign sales contracts, execute sales contracts, timely communicate with customers about project progress, and actively deal with relevant pre-sales and after-sales services;
3. Carry out professional promotion in the market;
4. Collect market information and changes, and report to the leader in charge in time;
5. Learn product knowledge, participate in product knowledge training, and correctly transfer the company's product information;
6. The establishment and improvement of relevant customer files shall be ensured to be complete, clear and timely submitted to the relevant person in charge.

Main responsibilities

1. College degree or above in medicine, biology or other related majors;
2. Experience in medical devices and other related work is preferred; Customers with certain resources are preferred;
3. Master certain sales skills, have strong customer service concept, and can provide good consultation, communication and coordination services for customers;
4. Hard working, serious, strong sense of responsibility, good team spirit, able to withstand certain work pressure, willing to accept challenges;
5. Have the spirit of pioneering, dedication and cooperation.

*Send resume to email： zhenzhen.wang@orientgene.com

Job requirements

1. According to the company's registration plan and process, carry out the registration work in an orderly manner and complete the company's product registration;
2. Collect, interpret and update relevant domestic registration laws and regulations;
3. Compilation and summary of registration materials;
4. Communicate and coordinate with the Drug Administration and other departments to track the progress of product registration;
5. Be responsible for the tracking of product registration testing, clinical validation, and the collection of results;
6. Be responsible for the filing, management and maintenance of registration materials and registration certificates;
7. Cooperate with the quality department and other relevant departments to audit the company's quality system by various audit institutions.

Main responsibilities

1. College degree or above in medicine, biology, engineering or other related majors;
2. Familiar with NMPA regulations and medical device product registration process, with more than one year of product registration experience, with instrument registration experience is preferred;
3. Familiar with the medical device quality management standard ISO9001 and ISO13485 is preferred;
3. Have strong independent learning ability and resistance to pressure;
4. Have good writing skills and solid writing skills, and be able to write relevant documents skillfully;
5. With a high sense of responsibility and service, careful and rigorous, strong logical thinking ability, good at expression and communication, strong organizational and coordination ability

*Send resume to email： zhenzhen.wang@orientgene.com