
CURRENT JOB LISTINGS
(Last updated 1/5/2009)
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Kuhn Med-Tech is currently recruiting for these and other positions
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Research & Development - Mechanical
1477
R&D Engineer
Southern California - Ophthalmic products.
IOL or contact lenses exp. Must have CNC Program exp. Hands-on; concept
to pilot run. Solidworks exp. Small component machine injection molded
products. B.S. or M.S. in Mechanical Engineering. Four to six yrs exp.
1481
R&D Project Mgr.
Southern California - Catheters
Will manage individuals from entry level to med-level exp., develops products,
researches new ideas, and establishes process development. Focus is on both
theoretical and practical solution development through the application of the
scientific process and directing subordinates toward clear objectives.
B.S. Bioengineering or equivalent. 4-8 yrs exp in medical device industry.
Exp. in Neurointerventional procedures.
1482
R&D Engineer
Southern California - Catheters
Will support development of products for medical device with work including
writing or verifying specifications, designing new products, designing fixtures,
test processes, equipment and raw materials to ensure the concepts and/or
prototypes meet their requirements. Degree in related field or equivalent.
3-5 yrs related exp. Computer skills including Word, Excel and CAD (Solidworks
or PRO/E proficiency required).
1483
R&D Technician
Southern California - Catheters
Fabricate prototypes, pilot units, qualification units and validation units.
Records test results on standard forms and writes test reports describing
procedures used. Provide support for the development of new products.
Interface with assemblers to teach new procedures. 3-5 yrs assembly or
hands-on technician work. Prior exp. in a medical device industry.
General computer skills including Word, Excel and Access.
1486
R&D Project Engineer / Sr. Product Development Engineer
Southern California - Neurovascular catheters
This position is responsible for the product design and development of catheter
devices for embolic protection. Carotid Artery Embolic Protection Catheter,
Acute Stroke, Thrombectomy Catheter. BS ME or similar field with 5+ yrs
exp or MSME with at least 3+ yrs exp. Minimum of three yrs exp. in
catheter design. Working knowledge of FDA / GMP and ISO regulations
(Design Controls). Computer skills to include spreadsheets, word
processing, project scheduling, AutoCad and Solidworks.
1492
Sr. Product Development Engineer
Southern California - Catheters.
Responsibilities include designing and developing least invasive surgery. This
will include part design, material selection, detailed drawing, fabrication
methods and vendor selection and coordination with an eye toward large scale
manufacturing (i.e. molding stamping). The design documentation will need
to comply with governing standards including FDA guidance, Quality Systems
Regulations, GMP and ISO. BSME. 8 to 10 yrs. medical device exp.
Demonstrated proficiency in mechanical design, DFM, and specification
development, preferred exp. in endoscopic or related device.
Research
& Development - Electronics / Software
1474
Principal Level Analog Design Engineer
Southern California - Therapeutic products.
Plant / integrate DFx requirements into production design requirements
specifications. Plan and coordinate system integration / test / debug.
Plan and coordinate verifications and validations. Design robust,
reliable analog circuit boards. Minimum BS Electrical Eng. MS preferred.
Minimum 10 yrs exp. in an engineering design environment. Worst case
analysis exp. Stepper motor driver design exp. Switch mod and
linear power supply design exp. Circuit board test and verification.
Exp. in DFT, DFM and DFR.
Manufacturing / Operations
1489
Sr. Mfg Engineer
Southern California - Catheters
Will develop and improve manufacturing methods, systems, and processes to
produce a high quality product at optimal cost. Act under limited
supervision of VP of Operations on multiple assignments of complex and broad
scope. B.S. from a four-year college or university, and 3 yrs related
exp. Exp. in transfer of pilot stage products into production.
Exp. in fabrication of medical devices in clean room and other manufacturing
environments.
Quality / Regulatory / Clinical Affairs
1470
Regulatory Affairs Mgr.
Bay Area - Cardiovascular.
Will manage the company's regulatory affairs department as directed by the Vice
President of Regulatory Affairs and Quality Assurance. Oversee the
preparation of new and audit / improve existing Technical Files and/or Design
Dossiers. Prepare new domestic regulatory submissions including, but not
limited to, 510(k) submissions, IDE's facility registrations, and other annual
reports as necessary. Perform internal quality audits in support of QSR
and ISO 13485:2003 compliance and the Quality Assurance function.
Sales & Marketing
Currently there are no Sales or Marketing positions at this time.
1465
Director R&D
International - Insulin Pumps.
Will lead a team to develop a new generation of insulin pump. BS or MS in an
Engineering field. Minimum 5 yrs. work exp. in insulin pump and related medical
device industry. Must be fluent in Chinese. Will work in Shanghai, China.
1480
Director of Regulatory Affairs
Southern California - Pharmaceutical, Cardiovascular
Will be responsible for the company's regulatory interactions in the U.S. and in
Europe. Act as primary contact with the FDA. Selection and management of
external consultants to assist in the development of global regulatory strategy
for the company's development programs.
MS / PhD / Pharm D.
Minimum of 8-10 yrs exp. in drug development. Minimum 5 yrs. exp. in
regulatory affairs with pharmaceutical company and/ or regulatory agency.
Significant role in the compilation of at least 1 IND and NDA.
Strong strategist in RA. Some start-up or small company exp.
HERE ARE SOME PREVIOUS POSITIONS FROM KMT THAT ARE NOW CLOSED
Please E-Mail your Résumé or Job Description to "new@kuhnmed-tech.com"
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