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EUROPLAZ TECHNOLOGIES is looking for employees for positions:
project engineer
project engineer
quality engineer
Working hours
full-time | Permanent
Requirements
proven ability to manage multiple projects simultaneously and meet tight deadlines
ability to dissect complex problems and employ a methodical approach to solution development
qualified in an engineering or technical discipline
excellent communication skills, both written and verbal
strong organisational and time management skills and ability to manage own workload independently
knowledge of quality systemssuch as ISO9001, ISO13485, MDD/MDR, CFR Part 820 & ISO14971
experience of applying Quality Tools and Techniques within a relevant industry – e.g. FMEA, RCA, CAPA, 8D, APQP, 5 Why, MSA, Statistical Analysis
working Hours: 40 per week
Responsibility
support the Regulatory Affairs Manager to create and maintain product Technical Files in accordance with requirements
maintain and improve the company's Quality Management System and internal processes
lead targeted problem-solving activities to address specific problems as and when they arise during development and in production
europlaz is a leading contract medical device manufacturing company operating under ISO 13485. Join us as a Project Engineer and contribute to delivering world-class medical devices that improve patient outcomes
lead Change Management activities ensuring robust adherence to all processes and applicable requirements
support the Europlaz / Customer driven Validation / Verification processes to ensure a successful and timely conclusion using the output from the process as the input into the in-process inspection criteria, sample size and frequency, etc
other various quality-based tasks as directed by the Quality Manager
support adherence to the company’s Internal and Supplier Audit schedules and the implementation of robust actions to address and follow up on any issues raised
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