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Quality Engineer III Irvine United States,  


Posted on : 07 May 2017

Project Description

Tracking Code Q17-024 Job Description The Quality Engineer III is responsibilities for risk management activities including FMEA analysis and post market surveillance. In addition, the position will support on-going departmental and/or improvement projects, new product introduction, document updates, assurance of compliance to current and changing regulations, and validation support as required Required Skills Bachelor’s degree or equivalent in a related technical discipline. 5+ years experience or equivalent combination of education and experience. Full knowledge of and application of principles and theories of quality engineering. Thorough understanding of GMP/ISO regulations and validation regulations is preferred. Quality Engineering, Six Sigma Green or Black Belt Certification preferred. Working knowledge of the device/drug/biotech manufacturing process. Skilled in statistical methods, statistical process control and sampling plans. Communication, technical, and computer skills. Coordination, tact and team work. Manual dexterity. Required Experience EEO/AA Employer/Veterans/Disabled/Race/Ethnicity/Gender/Age   To all recruitment agencies:  Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Staffing Representative. Please do not submit resumes unless authorized to do so.  Bio-Rad will not pay for any fees related to unsolicited resumes. Job Location Irvine, California, United States Department QSD IRV Quality Management (10185) Position Type Full-Time/Regular

Locations

Irvine, California, United States

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