Hi,

 

We have an opening for.......

 

Position: Software Quality Engineer with Certification

Location: Northridge, CA

Duration:  6 Months

Job Duties :  Conducts Continuous Improvement Reviews, Conducts root cause
analysis on specific project areas,Determines the need for - and provides -
QSR compliance and SQA support ,Ensures appropriate review of software
products ,Identifies and documents noncompliance ,Implements improvements in
processes, standards, and procedures, Monitors quality of software products,
processes, and standards,Performs in-process and phase end
assessments,Provides Part 11 compliance support ,Recommends improvements in
processes, standards, and procedures ,Supports SW development validation
lifecycle ,Facilitates and participates in qualification of acquired SW and
SW tools 

Skill Sets:

Certifications/ Engineering:

 QS, 21CFR - GMP/QSR, 29/40CFR, title 8, and NRC Compliance (Health Care)

Education Level:                                   Graduate Degree
Industry Experience:                             3 - 5 Years

Oral Communication:                            Excellent 

Software Application Knowledge/Engineering:   Acrobat Reader, MS Outlook, MS
Visio, MS Word, MS Access, MS Excel, MS PowerPoint, MS Project

Travel:  0-10% Travel

Written Communication: Excellent

Certifications/ Engineering: ASQC

Design Controls, DHF, and Engineering Documentation

PE - Professional Engineer, TQM

Development Tools: C Sharp, C++, Delphi

Factory Works: Frame Maker, Lab Windows, Lab view, MS Visual Basic, MS
Visual C++, MS Windows CE, MS Windows NT,

Education Level:

 Technical Certification 

 Quality or Reliability Certification

 Industry Experience:

 Greater than 5 Years /Oral Communication:/ Facilitation Skills /
Interviewing Skills

 Software Application Knowledge/Engineering:

 MS Exchange

 Major factors: a seasoned individual with strong skills in NEW Software
Life Cycle, and Risk Management, Standards (FDA, IEC and ISO standards
concentration in ISO-13485, 14971; IEC62304 and 21 CFR Part 820 and Part
11). Profundity in standards with EUMDD/International experience should be
evident. Proactive and results oriented professional, well-informed in New
and revised national and international standards applicable to Medtronic
MiniMed products during product realization or post market release . An
advocate of standards for products, services, processes, materials and
systems, and for conformity assessment, managerial and organizational
practices. FDA regulations, project management, risk analysis, and quality
assurance experience in accordance NEW Software Life Cycle. Candidate shall
have excellent communication and interpersonal skills. A potential candidate
shall have traits of technical mastery, strategist, cultivator and
innovator. 

 Please send me your Updated Resume and these details ASAP:

Full Name: 

Contact No:

E-mail ID: 

Availability:

Visa Status/Citizenship:

Current Location:

Best Rate

 

 

Regards,

 

SAM

Ling Technologies, Inc. I 9161 Liberia Ave, Suite 200 Manassas, VA 20110
Work: 703-880-8775 Fax Toll Free 866-473-6904 or 703-935-6082 I 

 <mailto:[EMAIL PROTECTED]> [EMAIL PROTECTED] I www.ling-tech.com
<http://www.ling-tech.com/>  I IM (No Emails on these IDs Please):
[EMAIL PROTECTED] I [EMAIL PROTECTED]  

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