Quality Engineer Dublin Medical Devices

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Role: Quality Engineer

Location: Dublin

Contract: 12month Fixed Term

Industry: Medical Devices

Key ResponsibilitiesThe main duties include but are not limited to the following:- Support Operations through the product life cycle / process for defined product portfolios

- Management of process deviations, non conformances, reworks, CAPA, Design - - Changes, complaints, scrap and change requests for product group

- Lead and/or proactively participate in cross functional investigations as required

- Lead and/or proactively participate in risk management activities for designated product groups and processes as required

- Support Validation activities for designated product groups

- Conduct process and GMP audits and ensure area compliance

- Liaise with regulatory department to ensure product supply is maintained and all quality aspects are met

- Champion QA and continuous improvement initiativesYour experience will look like:

- Proven experience in a Quality engineering role within the medical devices space

- Excellent verbal and written communication skills

- In-depth knowledge of International Standards, GLP and GMPThanks for taking the time to read.If this is not for you but you think you might know someone more suited I would be delighted if you could pass it on. Please click here to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement.To find out more about Real please visit www.realstaffing.comReal Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales