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Senior Quality Auditor

World Class Corporation with multiple
manufacturing, R&D and vendor sites. Plan,
execute, perform, report, and achieve corrective
actions for individual site, Divisional group,
supplier and Corporate audits. Participation on Product Development Teams to support new
products, vendor start-ups, new systems,
corrective action plans, and other assessment
activity. Project work for Global Quality
Assessment. Development new and revised
standards that affect business units and
suppliers. Some training of other groups. Will
assess regulatory, ISO and internal standards.

Requirements: BS degree in a scientific or
engineering discipline or equivalent experience. Experience as an Auditor or Lead Auditor for
ISO9000 and GMP/QSR systems in a medical
device, food, pharmaceutical or cosmetic
environment. Good Laboratory Practices (GLP)
auditing experience a plus, not mandatory.
Computer literate with strong skills in word
processing, spreadsheet, and database software (MSOffice). 30% Domestic Travel, 10%
International Travel.