Matchtech

Quality Engineer

Recruiter
Location
Wolverhampton
Salary
Negotiable
Posted
10 May 2017
Closes
01 Jun 2017
Ref
EMP390124
Contact
Matthew Hackett
Discipline
Mechanical
Contract Type
Permanent
Hours
Full Time
Quality Engineer is responsible for controlling, issuing and maintaining all Quality requirements associated with the product value streams in order to support continuing flow. The position shall also require interface with customers & suppliers on a routine basis with travel requirements to the supplier when necessary.

Responsibilities:



The successful applicant will be responsible to the Head of Quality and will undertake the following activities: -



The primary activities of this role will include:



* Run as well as participating in suspect quality investigations, Quality Clinic meetings, using ACE tools as required and taking part in root cause investigation presentations.
* Manage Quality Notifications and disposition accordingly
* Conduct Manufacturing Process Reviews (MPR) assessments internally and in the supply chain.
* Creation and review of FAI reports
* Implementation of ZDP (Zero Defect Plan) actions across suppliers
* Support AMS & new projects In-Load
* Track Corrective Action closure
* Carry out any other duties as required to support general operations of the Supplier Quality Department



Requirements:



* Must be self-motivated, an effective communicator
* Candidate must have excellent verbal and written skills, be able to work well in a team environment and have the ability to work across various departmental functions within the company
* Must be able to compile technical information and prepare for communicating to management (familiarity with standard business software is required – MS Office: Outlook, Excel, Word, PowerPoint, etc.)
* The ability to read and interpret engineering drawings and other engineering technical data is required
* Candidate should have a basic familiarity with expectations associated with aerospace or other comprehensive quality assurance systems, including ISO9000 or AS9100
* Prior knowledge of or experience with manufacturing inspection processes and methods or clinic activity is a plus
* Experience conducting internal Quality audits or supporting Quality audits by external agencies/customers is a plus
* Familiarity with SAP and QIM functionality is a plus as these systems are integral to the Clinic process