Four Job Openings at EndoMaster (medical robotics company) in Singapore
EndoMaster Pte Ltd. is a medical robotics startup based in Singapore.
It is developing a novel robot-assisted surgical system that will
significantly advance current flexible endoscopic surgeries and enable
surgeons to perform incision-less surgery that could only be
performed by open or laparoscopic surgery before. EndoMaster has
tested its prototypes on several patients with very positive results.
The world?s first flexible endoscopy robotic surgery in the stomach
was successfully performed. Safety, precision, and ease of use were
significantly improved with the robotic system.
The EndoMaster team is made up of experienced medical device
professionals, engineers, and clinicians specializing in
Gastrointestinal Endoscopy. The company currently has multiple job
openings (1 Senior R&D Engineer, 2 R&D Engineers, and 1 Firmware
Engineer) and is seeking candidates with strong motivation and
initiative, and experience in working in robotics / medical device
companies. All positions are available immediately. The reviewing
process will continue until the positions are filled. Salary and
benefits are dependent on the experience and education level of the
applicant. The job will be based in Singapore.
If interested, please send a cover letter and resume to Colin Tan
(
colin.tan@endomastermedical.com) and reference "Senior R&D
Engineer", "R&D Engineer", or "Firmware Engineer" in the subject.
EndoMaster Pte Ltd.
http://endomaste<wbr>
rmedical.com
-----
TITLE:
Senior R&D Engineer
SUMMARY:
This position involves leading and participating in the design and
development of EndoMaster's robot-assisted surgical system in support
of company?s strategic plan.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
1. Lead engineering team in design and development of medical systems
on time and on budget
2. Effectively communicate work with management and the team
3. Work closely with a multidisciplinary team (R&D, Clinical
Affairs, Quality Assurance, Regulatory and Marketing departments) to
coordinate pilot production of new products and accomplish tasks
4. Apply mechanical engineering knowledge to the design and
development of new products as well as product changes and
enhancements which are consistent with a zero defect level
5. Solve mechanical engineering problems at the component level
through thorough evaluation and troubleshooting
6. Conduct testing utilizing new and existing test protocols
7. Generate written reports that can clearly contribute to the Design
History File
8. Complete product enhancement projects in a manner consistent with
corporate objectives
9. Contribute to the company?s intellectual property position via
invention and patent applications
10. Create procedures for assembly, inspection and testing of devices
11. Oversee and participate in the pilot and later stage production of
the device
12. Maintain accurate documentation of concepts, designs, drawings,
and processes
13. Maintain current knowledge of competitive technologies in
addition to medical, technical, and biomedical developments related
to company products
14. Provide mechanical engineering and technical support of products
introduced into both the domestic and international markets as well
as physician in-service programs
15. Provide engineering support in the resolution of product
complaints and/or safety issues
16. Oversee outside vendors and consultants as required
17. Maintain GMP systems, including production quality assurance
procedures, pre-clinical testing programs and post-production GMP
compliance in coordination with the Document Control, Clinical, and
Quality Assurance functions
18. Support company goals and objectives, policies and procedures,
Good Manufacturing Practices, and European and FDA regulations
QUALIFICATIONS (EDUCATION, EXPERIENCE, SKILLS):
* Bachelor's or Master's degree in Mechanical Engineering or related
field with working knowledge of SolidWorks
* Finite Element Analysis knowledge is a plus
* 5 years or more of industry experience in engineering field
* Robotics and/or medical device experience preferred
-----
TITLE:
R&D Engineer
SUMMARY:
Use mechanical engineering knowledge to design, develop, and
manufacture EndoMaster's robot-assisted surgical system in support of
company?s strategic plan.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
1. Apply mechanical engineering knowledge to the design and
development of new products as well as product changes and
enhancements which are consistent with a zero defect level
2. Solve mechanical engineering problems at the component level
through thorough evaluation and troubleshooting
3. Conduct testing utilizing new and existing test protocols
4. Generate written reports that can clearly contribute to the Design
History File
5. Effectively communicate work with management and the team
6. Work closely with a multidisciplinary team (R&D, Clinical
Affairs, Quality Assurance, Regulatory and Marketing departments) to
coordinate pilot production of new products and accomplish tasks
7. Complete product enhancement projects in a manner consistent with
corporate objectives
8. Contribute to the company?s intellectual property position via
invention and patent applications
9. Create procedures for assembly, inspection and testing of devices
10. Oversee and participate in the pilot and later stage production of
the device
11. Maintain accurate documentation of concepts, designs, drawings,
and processes
12. Design and/or implement fixtures and equipment to aid in device
assembly
13. Maintain current knowledge of competitive technologies in
addition to medical, technical, and biomedical developments related
to company products
14. Provide mechanical engineering and technical support of products
introduced into both the domestic and international markets as well
as physician in-service programs
15. Provide engineering support in the resolution of product
complaints and/or safety issues
16. Assign work to technicians and temporary workers as needed
17. Oversee outside vendors and consultants as required
18. Maintain GMP systems, including production quality assurance
procedures, pre-clinical testing programs and post-production GMP
compliance in coordination with the Document Control, Clinical, and
Quality Assurance functions
19. Support company goals and objectives, policies and procedures,
Good Manufacturing Practices, and FDA regulations
QUALIFICATIONS (EDUCATION, EXPERIENCE, SKILLS):
* Bachelor's or Master's degree in Mechanical Engineering or related
field with working knowledge of SolidWorks
* Finite Element Analysis knowledge is a plus
* 2-5 years of industry experience in engineering field
* Robotics and/or medical device experience preferred
-----
TITLE:
Firmware Engineer
SUMMARY:
Use software engineering knowledge to design, develop software systems
for EndoMaster's robot-assisted surgical system in support of
company?s strategic plan.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
1. Apply software engineering knowledge to the design and
development of new products as well as product changes and
enhancements which are consistent with a zero defect level
2. Solve software/firmware problems through thorough evaluation and
troubleshooting
3. Assemble and test a real-time capable system platform for product
control and testing
4. Generate written reports that can clearly contribute to the Design
History File
5. Effectively communicate work with management and the team
6. Work closely with a multidisciplinary team (R&D, Clinical
Affairs, Quality Assurance, Regulatory and Marketing departments) to
coordinate pilot production of new products and accomplish tasks
7. Complete product enhancement projects in a manner consistent with
corporate objectives
8. Contribute to the company?s intellectual property position via
invention and patent applications
9. Create procedures for implementation and testing of devices
10. Participate in software implementation for the pilot and later
stage production of the device
11. Maintain accurate documentation of concepts, hardware, programs,
and processes
12. Design and oversee firmware for each stage of the system
13. Maintain current knowledge of competitive technologies in
addition to medical, technical, and biomedical developments related
to company products
14. Provide software engineering and technical support of products
introduced into both the domestic and international markets as well
as physician in-service programs
15. Provide engineering support in the resolution of product
complaints and/or safety issues
16. Oversee outside vendors and consultants as required
17. Support company goals and objectives, policies and procedures,
Good Manufacturing Practices, and FDA regulations
QUALIFICATIONS (EDUCATION, EXPERIENCE, SKILLS):
* Bachelor's or Master's degree in Computer Science, Electrical
Engineering, or related field with a deep understanding of real-time
operating systems with extensive experience of real-time programming
* 2-5 years of industry experience in engineering field
* Proficient in C Programming Language
* UDP/IP, CANOpen, microcontroller programming experience is a plus
* Must have gone through at least one whole product design process
* Experience with UL 2601/IEC60601 is advantageous
* Robotics experience and basic knowledge in control preferred
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