Quality Engineer 

About the Company

In this Medical device company, you will provide Quality Engineering support to the R&D, Manufacturing teams, Design Engineers and clients. Ideally you will bring some previous experience in a Medical Devices environment.

About the Position

Key Responsibilities

• Provide Quality support to project manager, design engineers, production manager and clients.
• Establish compliant product specifications.
• Quality review of validation plan, company reports and protocols.
• Co-ordinate compliant product risk management files.
• Issue and review manufacturing records.
• Co-ordinate and review of testing and release of sterile product.
• Quality review of SOP'S.
• Review and approve of product change controls.
• Advise on quality related issues with clients.
• Perform CAPA reports.
• Conduct internal audits.

Experience/Requirements

• Minimum level 8 degree in Science or Engineering discipline.
• 3-5 years medical device experience.
• ISO 13485 knowledge.
• Internal & external auditing experience.
• Validation experience (Sterilization, packaging)
• Ability to work on own initiative.
• Demonstrate detailed working knowledge of medical device environment. 
• Excellent communication skills.

Remuneration Package

• Strong competitive salary
• Occupational Company Pension Scheme
• Health Insurance
• Continued Professional Development Support
• Educational Assistance
• Annual Leave service increment
• Subsidised Sport & Social Club
• Bi-annual Company events
• Employee Well being Programme of Events
• Flexible Working Policy (includes the option to apply for Flexi-Time, Flexible Working Hours and Remote Working)

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