Description
Responsibilities for the Quality Engineer will include:
- Provide Quality Engineering support for validation and verification activities for existing and new production processes.
- Provide Quality Engineering support for process improvement activities both internally and liaising with suppliers.
- Process capability studies and analysis, setting bench marks and best practice.
- Provide Quality Engineering support and training where required, leadership for inter-departmental projects
- Monitor and report any transient areas of risk
- Adherence to Quality Management System (QMS) requirements in line with ISO13485 QMS & Good Manufacturing Practice (GMP) FDA21 CFR Part 820
- Ensure that process & timeline requirements for Corrective & Preventive Actions (CAPA) are met in accordance with the clients Standard Operating Procedures (SOP's) and in support of Global Objectives for CAPA.
The ideal NPI Quality Engineer will have experience
- Working predominantly within a Manufacturing support and New Product Development environment
- Experience of Design for Manufacture process
- Working with PFMEA's & Compiling Control Plans
- Understanding of manufacturing engineering and engineering drawings (GD&T)
- Understanding of metrology methods and inspection equipment
- Understanding of Manual and CMM inspection
- Understanding of Measurement Analysis techniques
- First Article Inspection reports/process (FAIRs)
- Process Validation & Verification
Qualifications/skills required for the Quality Engineer:
- Quality/Engineering qualification; preferably HNC/HND
- PC literacy, including specific knowledge of Microsoft products
Vivid Resourcing are committed to equality of opportunity for all applications from individuals are encouraged regardless of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships or any other characteristic protected by law.