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Accountancy
0 Agriculture, Fishing
0 Finance, Insurance
0 Call Centres
0 Catering & Hospitality
0 Construction, Property
0 Customer services
0 Defence/Armed Forces
0 Education
0 Electronics
0 Engineering, Manufacturing 0 Graduate, Trainees
0 Healthcare & Nursing
0 Human resources
0 IT & Internet
0 Legal
0 Management consultancy 0 Marketing, Advertising, PR 0 Media, Creative
0 Non-profit, Charities
0 Public sector & Services
0 Recruitment sales
0 Retail, Wholesale
0 Restaurant & Food Service 0 Sales
0 Science
0 Secretarial, Administration 0 Security
0 Senior appointments
0 Telecommunications
0 Transport, Logistics
0 Travel, Leisure, Tourism
0 Other
0
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Section: Other Vacancy 985 |
Post:Quality Engineer |
Salary contractual |
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Requirements and conditions |
Age: |
Has no value
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Gender |
Has no value
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Education: |
no
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Work schedule: |
Has no value
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Work place: |
London
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The announcement text: |
International Medical Device company located in Westchester County, NY is currently seeking a Quality Engineer to join their Quality Assurance and Regulatory Affairs team. The Quality Engineer is resposible for:
•Managing and updating site documentation
•Managing customer complaint investigations.
•Writing and coordinating efforts for the development and implementation of new and updated Quality System procedures for ISO/QSR compliance.
•Internal Audit Program participation - work with the established audit plan to assign auditors, oversee audits, and prepare audits reports.
•Oversight of the Corrective and Preventive Action System.
•Actively participating in the Supplier Management program; acts as the Technical Specialist to Materials in supplier-related quality issues.
•Material Review Board - facilitate MRB activities through review of nonconforming matierial and disposition.
•Perform Inspections of finished goods from suppliers
Qualified candidates will possess:
•Bachelors Degree in a scientific or technical discipline.
•5 years minimum experience with a quality system designed to meet the requirements of the FDA Quality System Regulation and ISO 13485/9001.
•Supportive Regulatory experience with a medical device manufacturer preferred.
•Strong skills in technical writing
•Strong interpersonal skills and respect for confidentiality
•ASQ Certification as a CQE or CQA desired.
•Training as an Internal Auditor
This is a temp-to-perm opportunity, salary range $50-65k depending on experience. Please e-mail your resume to wsrecruit@customstaffing.com.
http://www.customstaffingofwestchester.com/main.html
Location: Westchester County
Principals only. Recruiters, please don`t contact this job poster.
Please, no phone calls about this job!
Please do not contact job poster about other services, products or commercial interests.
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Contact information |
Employer: |
ElitPersonal
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Email: |
wsrecruit@customstaffing.com.
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Phone: |
8(044)586 48 66
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Publication date: 2010-01-26 04:58:47
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