Quality Engineer

Andover  ‐ Onsite
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Description

A 4 month contract has become available for an ambitious Quality Engineer for a leading medical device manufacturer. Get in touch if you would like to join an up and coming organisation as a Quality Engineer.

ESSENTIAL DUTIES AND RESPONSIBILITIES
  • Auditing (internal and supplier preferably)
  • CAPA processes - leading and participating, reviewing for compliance etc.
  • Non- conformance investigation and reporting
  • Document/change control
  • Complaint investigation
  • SOP review and development
  • Training


DESIRED MINIMUM QUALIFICATIONS / EXPERIENCE

The requirements listed below are representative of the knowledge, skill, and/or ability required for this position.
  • Preferably degree qualified ( Science or Engineering) but equivalent industry experience will be considered
  • Must have 2+ years recent experience in quality assurance within the medical devices industry
  • Good working knowledge of FDA Quality System Regulation and ISO13485, ISO14971
  • Must have good interpersonal skills and ability to work at all levels within the organization
  • Strong Microsoft Office skills
  • High level of attention to detail


If you are interested in this role, have any questions about this position or would like to register your interest in other positions, please feel free to send your up to date CV or contact me on

To find out more about Real please visit www.realstaffing.com
Start date
05/2013
From
Real Staffing
Published at
11.05.2013
Project ID:
534992
Contract type
Freelance
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