 |
 |
 |
 |
and understand new technologies relating to medical device design, flow
cytometry, electronics, optics and fluidics. In the area of documentation,
incumbent will be responsible for following GMP documentation guidelines when
maintaining documentation of CCS. Documentation includes: part specification,
part master system, assembly drawing, assembly procedures and test procedures.
The successful candidate will have expertise in flow cytometry system
development and manufacturing. This will include extensive expertise in
development of analog, power and digital electronics, mechanical systems,
fluidics, optics, software and system level testing. Knowledge of mixed analog
and digital PB design is essential. Experience with instrument safety agencies
and EMI/EMC testing is required. The successful candidate will have five to
eight years of relevant technical experience plus a minimum of two years
experience in project management. BS in engineering required; MS preferred.
Kindly mail or fax resumes to:
SyStemix, Inc.
3155 Porter Drive
Palo Alto, CA 94304
ATTN: Human Resources
(415) 813-4121
|
|
|
|