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 QUALITY CONTROL

Details
Country: USA
Location: Los Angeles CA
Total applied: 40
Location:US-CA-Los Angeles

Base Pay:N/A
Employee Type:Full-Time Employee

Industry:Other Great Industries

Manages Others:no
QUALITY CONTROL

QUALITY ASSURANCEENGINEER Full Time with Bios-Medical Co. Write/review/revise product procedures. Ensure quality records are clearly defined & accurately reflect all critical process events. 5+ yrs Q.A. exp in a cGMP, ISO13485 regulated Medical Device Mufactring environment. Requires a strong knowledge of manufacturing quality system reqmts, statistical techniques, data analysis + techniques, data analysis + continuous disciplines. Salary range 45-60K. DOE Great Benefits. QUALITY ASSURANCE ASSOCIATE Full Time with Bios-Medical Co. Responsible or QA support of CAPA process and related quality records. Able to analyze process requirements & quality data sources, identify problems and trends, assign & track CAPA's to ensure successful, timely closure. 3+yrs of Q.A. CAPA work exp in a cGMP, ISO13485 regulated mfg. environment. Salary range 45-55K. DOE Great Benefits. Send/fax resume: ONE LAMBOA 21001 Kittridge St., Canoga Park, CA 91303 [Click here for email] Attn: HR Fax 818-702-6904 EOE Webb LA540257 Los Angeles Times 2006-09-16


Source - Los Angeles Times
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