工程师

工程师

副标题

Clinical position
Job: clinical support (animal experiment)
Job : clinical supervisor CRA
Number of recruits: 3

operating duty:

1. Through technical follow-up, help doctors complete high-quality surgery and improve patient safety;

2. Guide relevant personnel in preoperative discussion, case analysis, collection, management and feedback of animal experiment and clinical data.

3. Assist doctors to complete the preparation of academic literature and slides related to products

4. Be responsible for the product use training of clinicians

5. Be responsible for product knowledge training of internal employees

6. Assist the R & D department to evaluate the clinical effect of products under research


Qualifications:


1. College degree or above, major in veterinary medicine or clinical medicine is preferred, and excellent fresh students are considered;

2. Working experience in cardiology or imaging is preferred

3. Have a high sense of responsibility, good team spirit and good communication skills;

4. Have good communication and learning skills, and adapt to business trips.

Location: Shanghai

Number of recruits: 2

operating duty:
1. Conduct screening, start-up, monitoring and closing visits of the clinical center according to the test scheme, the scope of work specified in the contract, the requirements of SOP and GCP.
2. Evaluate the quality and integrity of the work of the clinical center, determine whether the clinical center carries out its work in accordance with the scheme and applicable laws and regulations, form a monitoring report, and timely report, deal with and solve relevant problems.
3. Responsible for animal experiment of products and animal experiment tracking;
4. Complete other tasks assigned by the company.

Qualifications:

1. Bachelor degree or above, major in clinical medicine is preferred, familiar with cardiac and vascular anatomy, physiology and pathology is preferred;
2. Familiar with the clinical, registration and supervision regulations and processes of medical devices and in vitro diagnostic reagents;
3. It is required to be able to actively, actively and comprehensively report the work progress, have good organization, coordination, communication and negotiation skills, and be able to solve sudden problems;
4. At least 1 year of relevant working experience in medical device enterprises and cro companies, having completed the whole process of more than one clinical trial project, and being familiar with clinical trial scheme design, CRF production, ethical approval, recruitment and enrollment, implementation conclusion and other relevant workers are preferred; Excellent fresh students are also welcome.
Engineer position
Job: Software Engineer

Job: Hardware Engineer

Number of recruits: 2

Job responsibilities:

1. Be responsible for the preparation, modification and improvement of relevant product software of the company.
2. Responsible for equipment commissioning, data integration and Software commissioning of the company.
3. Maintain the software problems of the company's existing products, track and repair them.

Qualifications:

1. Bachelor degree or above, familiar with at least one of the following development languages c#, Java or python.
2. Be familiar with a front-end development framework, angular, Vue or react, etc
3. Familiar with and used Net entityframework or spring development framework to understand the development method of separating the front and back ends.
4. Understand serial port / socket / can and other communication protocols
5. Proficient in using MySQL and other databases
6. English reading and writing ability
Number of recruits: 2

Job responsibilities:

1. Be responsible for the preparation, modification and improvement of relevant product software of the company.
2. Responsible for equipment commissioning, data integration and Software commissioning of the company.
3. Maintain the software problems of the company's existing products, track and repair them.

Qualifications:

1. Bachelor degree or above, familiar with at least one of the following development languages c#, Java or python.
2. Be familiar with a front-end development framework, angular, Vue or react, etc
3. Familiar with and used Net entityframework or spring development framework to understand the development method of separating the front and back ends.
4. Understand serial port / socket / can and other communication protocols
5. Proficient in using MySQL and other databases
6. English reading and writing ability
Quality department
Job: Quality Engineer
Job: document controller of quality department

Number of recruits: 2


operating duty:


1. Analyze, report and solve product quality problems;

2. Handle nonconforming products;

3. Establish / improve product related testing capabilities, including establishing test standards and verifying test methods and equipment;

4. Be familiar with quality analysis tools and be responsible for data analysis related to product quality;

5. Responsible for product design verification;

6. Be responsible for the quality control of product development process, control the input and output of each stage of R & D, and analyze improvement activities;

7. Participate in and plan various quality management activities.


Job requirements


1. Bachelor degree or above in medical devices, chemistry, pharmacy, biology, medicine and other related majors


1. Familiar

GMP or ISO13485 related requirements, more than 2 years related working experience

3. Experience in class III sterile / implanted medical devices industry or CE certification or QA management experience of animal derived medical devices is preferred

4. Good communication, organization and coordination skills

Number of recruiters: 1

operating duty

1. Be responsible for the management, distribution, recovery, sorting and archiving of company level controlled documents;
2. Be responsible for the implementation, inspection and supervision of the company's documents;
3. Work report, document sorting, preliminary review, signing and approval follow-up;
4. Assist in the operation of quality system;
5. Assist in system assessment;
6. Assist in the internal audit or self inspection of the company's internal quality management system;
7. Complete other tasks assigned by company leaders.

Job requirements

Men and women are not limited. Under 40. Education is unlimited. No professional restrictions.
1. At least two years working experience in document control is preferred;
2. Working experience in medical device industry is preferred;
3. Have strong word processing ability, be able to draft and write document management directory under guidance;
4. Have certain ability of organization, coordination, independent analysis and problem solving;
5. Be able to skillfully operate office software.
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