Careers
Join Our Team
Join Us, Create the Future Together
Trulive is committed to becoming a globally leading innovative enterprise in structural heart disease and vascular access interventional devices. We are looking for passionate and innovative talents to jointly advance medical technology and bring hope and health to more patients.
Benefits We Offer
Health Protection
Social insurance, supplementary medical insurance, annual physical examination, paid annual leave
Career Development
Comprehensive training system, clear promotion channels, overseas learning opportunities
Incentive Mechanism
Competitive salary, performance bonus, equity incentive, project bonus
Team Culture
Flat management, open and inclusive, technology innovation-oriented, work-life balance
Open Positions
Medical Technical Support
Responsibilities
- Provide clinical trial technical support for the company's products, including product loading, intraoperative support and physician training
- Communicate product R&D directions with the R&D team and support product development from a clinical perspective
- Participate in animal studies of R&D products
- Develop internal and external technical training programs
Requirements
- Bachelor's degree or above in a medical-related major; clinical medicine or medical imaging preferred
- Willing to travel and work under intraoperative radiation
- Good learning and communication skills
- Background in ultrasound imaging or cardiology technical support preferred
- Good English listening, speaking, reading and writing skills preferred
R&D Engineer
Responsibilities
- Responsible for R&D design, optimization and improvement of project products, preparation of technical documents and drawings, and development of raw materials, molds/fixtures and processing techniques; ensure products comply with relevant laws, regulations and quality standards
- Participate in performance verification testing and process confirmation during product development
- Responsible for in vitro evaluation of project products; participate in animal and clinical evaluations to provide technical support for clinical trials, registration applications and system audits
- Responsible for preliminary research, competitive analysis and product requirement analysis, and develop new device technologies and materials
- Prepare DMR/DHF documents throughout the product lifecycle and draft related patents
- Other tasks assigned by superiors
Requirements
- Bachelor's degree or above in mechanical engineering, polymer materials or related majors; 1-3 years of experience; outstanding master's graduates also considered; experience in minimally invasive interventional product development or other Class III sterile device development preferred
- Good teamwork spirit, strong sense of responsibility, good logical thinking, coordination, learning and problem-solving skills
R&D Engineer - Valve
Responsibilities
- Responsible for the structural design of parts for newly initiated products, including 3D and 2D mechanical drawings, defining part quality standards, placing part fabrication orders and technical communication with part processing suppliers
- Responsible for assembling prototypes of newly initiated products, formulating verification plans, conducting verification and recording results
- Carry out design iterations based on verification results
- Communicate face-to-face with clinicians, participate in animal studies and clinical trials
- Complete project documents in accordance with company management systems
- Communicate and coordinate project tasks with other functional departments per company policies
- Besides new projects, complete design and optimization of the company's other in-development or commercialized products as assigned by superiors
Requirements
- Bachelor's degree or above in mechanical or mechanical-related majors; experience in weak current (electronics) is a plus
- 4+ years of work experience for bachelor's degree holders, or 2+ years for master's degree holders; medical device industry experience preferred
- Good teamwork spirit, strong sense of responsibility, good logical thinking, coordination, learning and problem-solving skills
Medical Specialist
Responsibilities
- Lead in vitro evaluation and animal study evaluation during the R&D stage of medical devices
- Responsible for training physician teams for clinical-stage products
- Surgical support during clinical trials
- Responsible for medical support and data processing during clinical trials
- Draft registration-related documents for pre-clinical and post-clinical products
Requirements
- Major in clinical medicine; experience in surgery/interventional procedures preferred; outstanding fresh graduates also considered
- Good scientific research thinking; experience in hospital clinical departments preferred
- Participated in the design and execution of clinical trials for devices/drugs
- Good learning ability
Didn't Find a Suitable Position?
We always welcome outstanding talents to join us. Please send your resume to our recruitment email, and we will recommend suitable positions based on your background and experience.
