[robotics-worldwide] 4 Job Openings at EndoMaster (medical robotics company) in Singapore

Tomonori Yamamoto tomonori.yamamoto at endomastermedical.com
Tue Feb 26 00:35:55 PST 2013





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 at 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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