Our Client are a leading engineering business based in Warwickshire. The company currently require a talented Quality Engineer to join the business.
Responsible for maintaining the quality management system procedures for the facility.
Administer quality management system and corrective and preventive action system.
Administer quality management system for the facility, standard operating procedures and work instructions; adhering to document control and quality management procedures.
Provide Quality Engineering support for production projects, leading validation activity & change management.
Create and maintain metrology programs for a range of precision metrology equipment Surface Finish Analyzer, Air Gages and inspection techniques such as, Roundness Testing, and coordinate measuring machines.
Provide Quality System training to all site employees, and ongoing in QMS releases and updates.
Assist in the management of the CAPA system, lead the investigation of non conformances, and lead the CAPA plan for timely closure.
Lead the development and evaluation of Statistical Process control within the manufacturing facility.
Performs and documents First Article Inspections Requirements on new products or after changes to a process.
Perform internal and external audits.
Preparation of Quality performance reports.
Must have sustained experience working in Metrology/Validation role ideally in the Medical Device industry.
Experience from Automotive industry considered.
Previous experience of statistical techniques, use of precision metrology equipment, CMM programing, Gauge R & R.
Proven knowledge of equipment validation and software validation in the Medical/Pharmaceutical industry.
Competitive contract rates offered.
6 month Contract.
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As an Equal Opportunities employer we welcome applications from all suitably qualified persons regardless of their race, sex, disability, religion/belief, sexual orientation or age.