Employment Philosophy - Talent Planning - 乐普心泰医疗公司 
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Employment Philosophy

Employment Philosophy

Putting people first, respecting talents, and cultivating talents. People are the primary productive force of an enterprise.
Harmony inspires wisdom, while unity makes strength. We advocate embracing diversity, pooling related parties' efforts together, and seeking win-win cooperation.
The realization of people’s value is an important symbol of our success. We will strive to be an industry leader while cultivating talents.

Talent Planning

We respect the mechanism of survival of the fittest talents, and excels at discovering talents, cultivating talents, and appointing core talents, thereby effectively activating employees' initiative and sense of responsibility, motivating people to grow, building elite teams, and improving the enterprise competitiveness. By setting up appropriate environmental supports, favorable quality of managers, optimistic corporate culture, and complete evaluation system, the Company guarantees the fairness and objectivity of talent development and assessment mechanism, thereby establishing a long-acting talent development mechanism.

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Career Development

We adhere to the employment philosophy of "putting people first, respecting talents, and cultivating talents". We are devoted to providing our people with a multi-channel development platform and a sophisticated training system, and offer "two-way career progression sequence" channels. People are allowed to choose the professional technical sequence or general management sequence depending on their own requirements for career development, so as to give full play to their personal strengths and prove their own value in different areas. We organize professional trainings for internal and external positions to address people's requirements for career development in an all-round manner.

  1. Quality Engineer

    1. Participate in the perfection of the Company's quality system, and formulate and revise the quality system process and institution;

    2. Maintain and supervise the operation of the quality system of each department: assist the production and QC teams in maintaining the quality systems for routine production/inspection; assist the purchasing staff to ensure the quality of raw materials/suppliers is compliant with regulations and standards, and to assist the R&D team in the quality system building for new products;

    3. Participate in the Company's internal and external audits (by the National Medical Products Administration, the CE certification bodies, etc.), and lead the completion of various CAPAs;

    4、Maintain the validity of the medical device manufacturing license

     

    Qualification (Social recruitment):

    1、Bachelor's degree or above in medical devices, biomedicine, mechanics, polymers, metallic materials, etc.;

    2、At least 1 year of experience in quality/technology etc. at the production sites of sterile medical devices;

    3、Be familiar with the ISO13485 quality management system, as well as relevant Chinese and EU laws and regulations on medical devices;

    4、Excellent communication skills and ability to push/solve problems; team spirit.

  2. R&D Engineer

    1. Design, manufacture and improve machinery, molds, tooling and products; design and develop emerging products;
    2. Have the launched products continuously improved, and improve the quality of products;
    3. Master's degree or above in polymer science in pharmaceutics, etc.; be familiar with CAD software.

  3. Academic Supervisor/Specialist

    1. Organize, plan and implement activities such as academic promotion conference and training session; pay clinical visits and provide professional consultation; maintain the network of academic experts within the region of duty, and keep good communication with customers;

    2. Learn and understand the developments of clinical use of products in the region of duty; provide relevant advices and learn about the market feedback from customers, the marketing channels for products, and the market information of competitive products; perform market analysis, and bring forward suggestions for improvement of marketing and sales policies;

    3. Guide sales staff to carry out marketing promotion.

     

    Qualification:


    1. Bachelor's degree and above in medicine, news media, marketing and other related subjects;
    2. 3-5 years (or longer) occupational experience in the medical device industry;
    3. Excellent communication skills and learning capability; strong sense of responsibility and teamwork competency; passionate and confident, aggressive, and willing to travel.

  4. Medical Editor

    1. Independently write articles on hospitals, health, life, etc. for media platforms;

    2. Participate in online and offline activity creation, planning and effect evaluation;

    3. Keep fluent communication with each department of the Company, identify and report the market demand, and provide support at the level of academic article;

    4. Accomplish other tasks assigned by the leaders.

     

    Qualification:


    1. Bachelor's degree or above in literature, journalism & communication, clinical medicine, etc.; excellent fresh graduates are also acceptable;
    2. At least two years of hands-on experience in relevant practices; those with cardiovascular industry are preferred; those who are familiar with new media operation procedure or experienced in new media/We-Media edit operation are preferred;
    3. Excellent writing and clear thinking; distinguished style of writing; excellent ability to integrate resource materials.

  1. Clinical Project Manager/Clinical Research Associate

    1. Perform and monitor clinical trials, keep track of the clinical progress of each center, and supervise & urge the implementation of clinical protocols; promptly and properly handle AE and SAE; solve the problems that arise during clinical trial, and process the clinical data;

    2. Assist supervisors to design, prepare and produce clinical trial protocols, CRF designs, investigator's brochures, and trial-related information; conduct the investigation & survey and screening of organizations for clinical study, and carry out agreement negotiation; convene meetings at various stages of clinical trials;

    3. Keep a solid relationship with clinical hospitals and related clinical trial staff.

     

    Qualification:


    1. Bachelor's degree and above in clinical application, nursing or pharmacy, and other related subjects;
    2. More than 2 years of occupational experience in clinical monitoring; those with experience in three types of medical devices are preferred;
    3. Learn and comprehend laws and regulations on GCP and clinical application;
    4. Excellent communication skills and strong sense of teamwork; accept appropriate business trips.

  2. Overseas Clinical Registration

    1. Compilation, collation, formal review, normative production and filing of product registration information, as well as the organization, compilation and filing of CE certification information;

    2. Follow up with the clinical validation of the product etc. and collect the results; seek communication and coordination with the National Medical Products Administration and other authorities to track the product registration progress, and coordinate the solving of problems in the review process;

    3. Prepare data and prepare and organize relevant information for the domestic registration and overseas certification of the Company's medical devices and IVD products (including the CE certification, the local registration for customers, etc.); participate in certification and maintain relevant data to ensure the successful declaration/testing/registration/certification/evidence collection, etc. for the products;

    4. Establish the product registration budget, work plan and schedule of the Company, monitor the progress of product registration, and solve the problems in product registration in a timely manner.

     

    Qualification:


    1. Bachelor's degree and above in medicine, pharmacy, English and other relevant subjects;
    2. Satisfactory English listening, speaking, reading and writing skills;
    3. More than 3 years of hands-on experience in registration/certification declaration of medical devices or pharmaceuticals; be familiar with the standards for domestic registration and international certification of medical devices; know the CE certification processes and procedures.

  3. HR Specialist

    1. Release recruitment information, screen resumes, organize and arrange the interview for candidates;

    2. Assist in the organization and implementation of various staff activities, as well as the completion of various reports and project reporting;

    3. Fulfill other tasks assigned by leaders.

     

    Qualification:


    1. Bachelor's degree in human resources, business administration, statistics, etc.;
    2. More than two years of experience in recruitment; those with experience in recruitment for the medical device/pharmaceutical industry are preferred;
    3. Stress tolerant; hardworking & industrious; motivated and eager to learn.

  4. Production Supervisor

    1. Assist the production manager to develop yearly, quarterly and monthly production plans and manage the trainings for production staff;

    2. Control the quality during production, effectively execute the quality system, and perform the maintenance and servicing of production environment and facilities & equipment, etc.

    3. Fulfill the tasks assigned by the production manager.

     

    Qualification:


    1. Junior college degree or above; junior college degree or above in biomedicine preferred;
    2. More than 3 years of experience in production line management; those with experience in production line management of the medical device industry are preferred;
    3. Be experienced in GMP (good manufacturing practice) and site management; know the requirements of specification on quality management of sterile medical devices; be familiar with ISO9001, ISO13485 and other quality management systems;
    4. Strong initiative and sense of responsibility; willing to grow with the Company.

  1. Process Technician

    1. Participate in product R&D based on the design & development plan;

    2. Verify or re-verify the production processes in R&D, instruct and supervise the execution of processes;

    3. Analyze the causes of substandard products in various production segments, and take corrective and improving actions; improve the production efficiency and product quality, and reduce the production costs through production optimization.

     

    Qualification:


    1. Junior college degree or above; be able to read drawings and use general tools such as vernier calipers;
    2. More than 2 years of experience in production process; those with experience in production processes of the medical device industry are preferred;
    3. Aged 20-35; healthy; good eyesight.

  2. Production Operator

    1. Operate forming and film stitching processes for the products;

    2. Fulfill the desired output indicators;

    3. No gender preference; high school degree or technical secondary school degree or above; healthy; good eyesight.

  1. R&D Engineer

    1. Design, manufacture and improve machinery, molds, tooling and products; design and develop emerging products;

    2. Have the launched products continuously improved, and improve the quality of products;

    3. Master's degree or above in polymer science in pharmaceutics, etc.; be familiar with CAD software.

  2. Marketing Specialist

    1. Participate in marketing promotion planning and execute online and offline activities; assist in coordination for various academic conferences;

    2. Assist the departments in writing articles on hospitals, health and life, etc. for media platforms;

    3. Bachelor's degree or above in medicine, news media, marketing, and other related subjects; those who accept regular business trips, are good at communication & expression, and have favorable copywriting skills are preferred.

  3. Clinical Specialist

    1. Assist in the data collection, sorting and archiving management for clinical trial projects;

    2. Assist in the screening & enrollment, monitoring and follow-up visit of subjects, etc. during clinical trials in hospitals;

    3. Bachelor's degree or above in medicine, biology, nursing or pharmacy; stress tolerance, and strong sense of responsibility.

  4. Quality Engineer

    Qualification:

    1. Assist leaders in the operation, maintenance and improvement of the Company's quality management system, and stimulate the fulfillment of quality objectives of the Company and its departments;

    2. Bachelor's degree or above in medical devices, biomedicine, mechanics, polymers, metallic materials, etc.

    3. CET6 and AutoCAD preferred; with excellent communication skills, stress tolerance and team spirit.

  1. Quality Engineer

    1. Participate in the perfection of the Company's quality system, and formulate and revise the quality system process and institution;

    2. Maintain and supervise the operation of the quality system of each department: assist the production and QC teams in maintaining the quality systems for routine production/inspection; assist the purchasing staff to ensure the quality of raw materials/suppliers is compliant with regulations and standards, and to assist the R&D team in the quality system building for new products;

    3. Participate in the Company's internal and external audits (by the National Medical Products Administration, the CE certification bodies, etc.), and lead the completion of various CAPAs;

    4、Maintain the validity of the medical device manufacturing license

     

    Qualification (Social recruitment):

    1、Bachelor's degree or above in medical devices, biomedicine, mechanics, polymers, metallic materials, etc.;

    2、At least 1 year of experience in quality/technology etc. at the production sites of sterile medical devices;

    3、Be familiar with the ISO13485 quality management system, as well as relevant Chinese and EU laws and regulations on medical devices;

    4、Excellent communication skills and ability to push/solve problems; team spirit.

  2. R&D Engineer

    1. Design, manufacture and improve machinery, molds, tooling and products; design and develop emerging products;
    2. Have the launched products continuously improved, and improve the quality of products;
    3. Master's degree or above in polymer science in pharmaceutics, etc.; be familiar with CAD software.

  3. Academic Supervisor/Specialist

    1. Organize, plan and implement activities such as academic promotion conference and training session; pay clinical visits and provide professional consultation; maintain the network of academic experts within the region of duty, and keep good communication with customers;

    2. Learn and understand the developments of clinical use of products in the region of duty; provide relevant advices and learn about the market feedback from customers, the marketing channels for products, and the market information of competitive products; perform market analysis, and bring forward suggestions for improvement of marketing and sales policies;

    3. Guide sales staff to carry out marketing promotion.

     

    Qualification:


    1. Bachelor's degree and above in medicine, news media, marketing and other related subjects;
    2. 3-5 years (or longer) occupational experience in the medical device industry;
    3. Excellent communication skills and learning capability; strong sense of responsibility and teamwork competency; passionate and confident, aggressive, and willing to travel.

  4. Medical Editor

    1. Independently write articles on hospitals, health, life, etc. for media platforms;

    2. Participate in online and offline activity creation, planning and effect evaluation;

    3. Keep fluent communication with each department of the Company, identify and report the market demand, and provide support at the level of academic article;

    4. Accomplish other tasks assigned by the leaders.

     

    Qualification:


    1. Bachelor's degree or above in literature, journalism & communication, clinical medicine, etc.; excellent fresh graduates are also acceptable;
    2. At least two years of hands-on experience in relevant practices; those with cardiovascular industry are preferred; those who are familiar with new media operation procedure or experienced in new media/We-Media edit operation are preferred;
    3. Excellent writing and clear thinking; distinguished style of writing; excellent ability to integrate resource materials.

  5. Clinical Project Manager/Clinical Research Associate

    1. Perform and monitor clinical trials, keep track of the clinical progress of each center, and supervise & urge the implementation of clinical protocols; promptly and properly handle AE and SAE; solve the problems that arise during clinical trial, and process the clinical data;

    2. Assist supervisors to design, prepare and produce clinical trial protocols, CRF designs, investigator's brochures, and trial-related information; conduct the investigation & survey and screening of organizations for clinical study, and carry out agreement negotiation; convene meetings at various stages of clinical trials;

    3. Keep a solid relationship with clinical hospitals and related clinical trial staff.

     

    Qualification:


    1. Bachelor's degree and above in clinical application, nursing or pharmacy, and other related subjects;
    2. More than 2 years of occupational experience in clinical monitoring; those with experience in three types of medical devices are preferred;
    3. Learn and comprehend laws and regulations on GCP and clinical application;
    4. Excellent communication skills and strong sense of teamwork; accept appropriate business trips.

  6. Overseas Clinical Registration

    1. Compilation, collation, formal review, normative production and filing of product registration information, as well as the organization, compilation and filing of CE certification information;

    2. Follow up with the clinical validation of the product etc. and collect the results; seek communication and coordination with the National Medical Products Administration and other authorities to track the product registration progress, and coordinate the solving of problems in the review process;

    3. Prepare data and prepare and organize relevant information for the domestic registration and overseas certification of the Company's medical devices and IVD products (including the CE certification, the local registration for customers, etc.); participate in certification and maintain relevant data to ensure the successful declaration/testing/registration/certification/evidence collection, etc. for the products;

    4. Establish the product registration budget, work plan and schedule of the Company, monitor the progress of product registration, and solve the problems in product registration in a timely manner.

     

    Qualification:


    1. Bachelor's degree and above in medicine, pharmacy, English and other relevant subjects;
    2. Satisfactory English listening, speaking, reading and writing skills;
    3. More than 3 years of hands-on experience in registration/certification declaration of medical devices or pharmaceuticals; be familiar with the standards for domestic registration and international certification of medical devices; know the CE certification processes and procedures.

  7. HR Specialist

    1. Release recruitment information, screen resumes, organize and arrange the interview for candidates;

    2. Assist in the organization and implementation of various staff activities, as well as the completion of various reports and project reporting;

    3. Fulfill other tasks assigned by leaders.

     

    Qualification:


    1. Bachelor's degree in human resources, business administration, statistics, etc.;
    2. More than two years of experience in recruitment; those with experience in recruitment for the medical device/pharmaceutical industry are preferred;
    3. Stress tolerant; hardworking & industrious; motivated and eager to learn.

  8. Production Supervisor

    1. Assist the production manager to develop yearly, quarterly and monthly production plans and manage the trainings for production staff;

    2. Control the quality during production, effectively execute the quality system, and perform the maintenance and servicing of production environment and facilities & equipment, etc.

    3. Fulfill the tasks assigned by the production manager.

     

    Qualification:


    1. Junior college degree or above; junior college degree or above in biomedicine preferred;
    2. More than 3 years of experience in production line management; those with experience in production line management of the medical device industry are preferred;
    3. Be experienced in GMP (good manufacturing practice) and site management; know the requirements of specification on quality management of sterile medical devices; be familiar with ISO9001, ISO13485 and other quality management systems;
    4. Strong initiative and sense of responsibility; willing to grow with the Company.

  9. Process Technician

    1. Participate in product R&D based on the design & development plan;

    2. Verify or re-verify the production processes in R&D, instruct and supervise the execution of processes;

    3. Analyze the causes of substandard products in various production segments, and take corrective and improving actions; improve the production efficiency and product quality, and reduce the production costs through production optimization.

     

    Qualification:


    1. Junior college degree or above; be able to read drawings and use general tools such as vernier calipers;
    2. More than 2 years of experience in production process; those with experience in production processes of the medical device industry are preferred;
    3. Aged 20-35; healthy; good eyesight.

  10. Production Operator

    1. Operate forming and film stitching processes for the products;

    2. Fulfill the desired output indicators;

    3. No gender preference; high school degree or technical secondary school degree or above; healthy; good eyesight.

  1. R&D Engineer

    1. Design, manufacture and improve machinery, molds, tooling and products; design and develop emerging products;

    2. Have the launched products continuously improved, and improve the quality of products;

    3. Master's degree or above in polymer science in pharmaceutics, etc.; be familiar with CAD software.

  2. Marketing Specialist

    1. Participate in marketing promotion planning and execute online and offline activities; assist in coordination for various academic conferences;

    2. Assist the departments in writing articles on hospitals, health and life, etc. for media platforms;

    3. Bachelor's degree or above in medicine, news media, marketing, and other related subjects; those who accept regular business trips, are good at communication & expression, and have favorable copywriting skills are preferred.

  3. Clinical Specialist

    1. Assist in the data collection, sorting and archiving management for clinical trial projects;

    2. Assist in the screening & enrollment, monitoring and follow-up visit of subjects, etc. during clinical trials in hospitals;

    3. Bachelor's degree or above in medicine, biology, nursing or pharmacy; stress tolerance, and strong sense of responsibility.

  4. Quality Engineer

    Qualification:

    1. Assist leaders in the operation, maintenance and improvement of the Company's quality management system, and stimulate the fulfillment of quality objectives of the Company and its departments;

    2. Bachelor's degree or above in medical devices, biomedicine, mechanics, polymers, metallic materials, etc.

    3. CET6 and AutoCAD preferred; with excellent communication skills, stress tolerance and team spirit.



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