Validation Engineer

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Role: Validation Engineer

Location: Cork

Contract: An initial 12 month hourly rate contract

The company:

The company are dedicated to transforming lives through leading medical solutions that improve patient's health worldwide. They provide a broad and deep portfolio of innovative products and services. They specialise in the manufacture of minimally invasive medical device.

The Role:

As a Validation Engineer, you would be responsible for the support and maintenance of the Validation Systems on site.

Responsiblities:

* Work alongside the Quality Engineering and Product Development teams.

* Execution of Validation Processes.

* Mitigation of risk / Risk Assessments.

* Provide support to the validation department in regards to decisions on systems that require validation.

* Identify areas for improvement and provide recommendations / advice about software solutions.

* Maintain procedures related to Software Validation; provide support to Process Validations in regards to OQ, PQ, PPQ revisions.

Requirements:

* 3 - 5 years' experience within the medical device industry.

* Risk management knowledge.

* Experimental Design experience.

* Communication and medication skills.

* A broad understanding of validation processes.

* A knowledge of both software and hardware validation processes.

* Have good leadership skills.

* A background in manufacturing processes.

No CV ready? Not sure yet? Feel free to contact me for more details.

To find out more about Real please visit www.realstaffing.com

Real 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