US-NJ: Fairlawn-Senior Electrical Engineer
JobCircle.Com
JobCircle.com - Careers, Content and Community for Technology
professionals in the Northeastern United States!
Jobcircle.com provides resume submission, classified searches,
eLearning, hundreds of career development articles, tech news,
and more to tens of thousands of Technology professionals in
your area - visit us today at http://www.jobcircle.com!
!!! Voted a TOP 50 Career Web Site in 2002 by CareerXRoads !!!
**************************************************************
Job Title: Senior Electrical Engineer
Job Location: NJ: Fairlawn
Pay Rate: open
Job Length: full time
Start Date: 2004-05-17
Company Name: The Judge Group
Contact: Sabreena Tressler
Phone: 732-346-9100
Fax: 732-346-9101
Description: If you have Call Intercept on your phone, please provide your password with your response/resume OR deactivate the service during your career search with Judge. Thank you in advance for helping us provide a more timely response to your interest in our job posting.
Judge Technical Services, Scientific Division provides high-end consulting and staffing services to fortune 500 companies. We have been retained by our client to seek and identify qualified candiates for a Sr. Electrical Engineer. Under the direction of Manager, Electronics Development will design and develop electronic medical devices for drug delivery applications. The incumbent will develop new products and associated intellectual property, and lead the development effort from concept through design, validation and manufacturing of the electronics / electromechanical components associated with those products.
Required Experience:
·BSEE with 6-8 years of experience in electronics design, development and manufacturing with increasing responsibility or equivalent. MSEE is desirable.
·Thorough understanding of software development (assembly language programming) associated with developing small electronics products. At least 5 years of hand-on experience in the design of medical device field is highly desirable including familiarity with the validation (including software validation) process. Having a good understanding of developing electro-mechanical systems is preferred. A strong knowledge of quality systems regulations, manufacturing, embedded software, hardware, and interconnect technologies. Excellent verbal and written communication skills. Knowledge of FDA QSR and GMP processes. Knowledge of EN 60601 (including EMC and other design standards) is desirable. Knowledge of and experience with FMEA and hazard analysis methods for electronics, software, and medical products. Previous involvement in a clinical trial to prove safety and efficacy of a medical device is highly desirable.
Project description:
-Drives the successful execution of a protocol using strong management and organizational skills;
-Monitors protocol progress and addresses/manages obstacles;
-Serves as primary contact for the protocol;
-Coordinates the development of protocol-level documents and plans;
-Effectively leads a global team of individuals assigned to the protocol
Skills:
Clinical Protocol Manager
Must Have 5-7 Years of Pharmaceutical Industry Experience
Protocol and Project Management in Pharm Industry/Clinical Development
Candidate with a BA, BS, or an MS Degree is Preferred
Required skills:
BS with 6-8 years of experience or a MS is desirable. Thorough understanding of software development (assembly language programming) associated with developing small electronics products. At least 5 years of hand-on experience in the design of medical device field is highly desirable including familiarity with the validation (including software validation) process. Having a good understanding of developing electro-mechanical systems is preferred. A strong knowledge of quality systems regulations, manufacturing, embedded software, hardware, and interconnect technologies. Excellent verbal and written communication skills. Knowledge of FDA QSR and GMP processes. Knowledge of EN 60601 (including EMC and other design standards) is desirable. Knowledge of and experience with FMEA and hazard analysis methods for electronics, software, and medical products. Previous involvement in a clinical trial to prove safety and efficacy of a medical device is highly desirable.
Please email me a resume with two references.
Applicant must be a U.S. resident or currently able to legally work in the U.S.
Please refer to Job code JO038472SXT when responding to this ad.
For FASTEST PROCESSING of your resume, please visit http://www.jobcircle.com/classifieds/472654.html to apply online.
**************************************************************
For fastest processing of your resume, this employer asks that
you apply to this job using the URL above.
**************************************************************