Strong Middle / Senior Quality Engineer

Description

Inviting Quality Engineer to join a growing account in the medical devices industry domain.

The client is one of the biggest manufacturers of medical devices in the US. The company produces a variety of medical devices and applications.

Requirements

• At least 3 years of IT industry experience (Quality/Process engineer or similar position from Quality or Process Management sphere);
• Good understanding of Risk Management principles and technics (Failure Mode and Effect Analysis (FMEA) and other);
• Ability to work with big amounts of information, produce and organize content in a logical flow;
• Strong documentation management skills, ability to analyze and interpret complex and complicated documents;
• Good analytical skills;
• Attention to details;
• Ability to cope with quite routine work;
• Team player;
• Experience in writing, proofreading and editing documentation.
• The ability to work independently
• Excellent communication skills, both written and verbal

English:

• Upper Intermediate or higher; ability to communicate with native speakers is a must;

Would be a plus:

• Product experience 
• Experience in creating and verifying of Human Factor documentation
• Technical background