Description
Requirements:- BS in Science or Engineering (or related field)
- Minimum of 5 years experience in areas of Process Development and Manufacturing Quality Engineering in the medical device industry or (related industry). Other experience related to engineering such as R&D or Manufacturing could also be considered.
- Strong understanding of ISO 13485
- Exceptional communication skills
- Strong mechanical aptitude and methodical problem solving skills
Responsibilities:
- Coordinate efforts to develop and continuously improve manufacturing processes using tools such as DOE, FMEA and SPC.
- Analyze product designs to assist in the development and optimization of process technologies
- Ability to identify and manage risk via FMECA or other risk management tools
- Lead investigations into non-conforming material
- Offers statistical guidance to test protocols and reports
- Provide engineering support to Sourcing Organization
- Review and create test plans and reports such as First Article Inspection, qualification, and validation
If you, or anyone you know are interested, please get in contact with me as soon as possible via email, as all first round interviews will be confirmed by the end of this week!
To find out more about Real please visit www.realstaffing.com