Compliance Auditor III

Job type:
on-site
Start:
04/2014
Duration:
24 Months
From:
Real Staffing
Place:
Temecula
Date:
06/03/2014
Country:
flag_no USA
project ID:
715652

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Key Features-

Must have a technical background, be familiar with applicable US and outside US regulations, standards, corporate and divisional standards. Specifically, the individual must have a working knowledge of Quality Systems Regulations (QSR) and International Standards (ISO13485). Additionally, the individual must understand a variety of quality/operational systems that support facility, product design, development, production, distribution, installation, and understand the principals of quality management.

Skills and Experience-

Bachelor degree (in Engineering or Medical Science preferred) or equivalent experience and sufficient exposure to pharmaceutical or medical device related industries required along with 4+ years relevant experience as an Auditor (Internal Compliance Auditor for example). Auditing Certification is also a requirement, such as ISO13485 Lead Auditor or ASQ Auditor certification or equivalent. Additional experience in a Quality Engineering and/or Manufacturing Engineering and/or Laboratory setting that has supported manufacturing sites for pharmaceutical or medical device related industries is preferred. Must have excellent oral and written communication skills.

This is an excellent opportunity to gain valuable experience working amongst industry leaders and exceptional professionals. Please submit your resume in order to be considered for a resume.

To find out more about Real please visit www.realstaffing.com