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Quality Engineer
Eingestellt von Real Staffing Group aus Frankfurt am Main
Gesuchte Skills: Support, Engineering, Engineer
Projektbeschreibung
* Perform nonconformance investigations to determine root case. Assign and ensure completion of corrective and preventive actions. Complete investigations in a timely manner to ensure customer service levels are maintained.
* Coordinate the reporting and provide trend analysis for nonconformance incidences
* Provide investigation and support for CAPA and Failure Investigation Reports
* Write out of tolerance investigations
* Write FMEAs, review and write protocols and reports for new products
* Perform audits of Production and Receiving Inspection areas
* Support environmental monitoring of cleanroom areas
* Qualify and implement document changes involving product or process changes
* Support Quality Control activities for Receiving Inspection, Production, Finished Goods, and Calibration
* Assist in supervisory activities of Quality Control personnel
* Leads the development of Risk Management documentation.
* Facilitates Risk Management meetings.
* Identifies hazards and mitigates risks associated with identified hazards in Design and Process FMEA.
Minimum 5 years experience in the medical device industry is preferred
BS in Engineering or related field
Working knowledge of U.S. and international medical device regulations is desirable
Working knowledge of EO Sterilization is desirable
Working knowledge of desktop computer office software and e-mail is required
Excellent verbal and written communication skills
Flexibility to handle multiple tasks and meet timelines
To find out more about Real Staffing please visit www.realstaffing.com
Projektdetails
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Einsatzort:
Irvine, California, Vereinigte Staaten
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Projektbeginn:
asap
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Projektdauer:
Keine Angabe
- Vertragsart:
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Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Sonstiges