Place of work: United Kingdom, Lancashire
Type of job contract: for an indefinite period, full-time

Required education:
Offered salary: Not specified
Number of positions: 1

Working area

Computing, engineering, science professionals
   Physical and engineering science technicians
        Electrical engineering technicians

JOB DESCRIPTION:

Quality Engineer Salary: £30,000 - £40,000 per annum DOE plus competitive benefits Quality Engineer / QA Engineer / Product Quality Location: Manchester / Cheshire / North West A Manchester/ Cheshire based company are currently seeking a Quality Engineer to join their team on a permanent basis. This is an excellent opportunity to join a fast growing Medical Device Manufacturer who design, develop and manufacture a range of innovative exciting products all on site. The successful applicant will be an excellent communicator and have the ability to use their initiative when making decisions. This role requires a Medical Device background and working knowledge of ISO 13485 along with a good understanding of root cause analysis techniques and problem solving, ability to facilitate / co- ordinate and drive project teams to successful outcomes. This opportunity will include monitoring and improvement of the company’s global supply chain, with potential travel, working closely with the technical, engineering and purchasing groups. Role and Responsibilities: Manage suppliers to reduce number of non- conformances and improve quality supply chain Liaise with internal and external resources in order to drive identification and implementation of related actions ( correction and corrective) in a timely manner Review and trend non- conformance system Conduct non- conformance related investigations Identify new or change existing supplier quality systems Conduct quality assessments of current suppliers Conduct internal and departmental audits Carry out inspections and investigations Experience and Requirements: Proven knowledge of ISO 13485 Team leading Practical approach towards problem solving Knowledge of continuous improvement techniques Good written, communication and computer knowledge and experience Must be able to communicate with all levels of the organisation GMP experience ( beneficial) FDA experience ( beneficial) Interviews can be arranged over the next week as they are keen to get the ball rolling.

Work hours:

  • Without entering work hours

Requirements




source: https://www.ec.europa.eu/eures

  
     


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