Quality Engineer
Vapotherm - Exeter, NH

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The responsibilities include assisting with the development of quality systems, procedures and controls to ensure that products consistently meet performance and quality specifications. The Quality Engineer is a leader and strong technical resource who will quickly, effectively and permanently resolve quality problems both internally at Vapotherm and externally at customers and suppliers.

Position Responsibilities
Works closely with R&D to ensure robust quality specifications for new products.
• Assists in writing, reviewing and executing design and process verifications and validations.
• Performs light mechanical design for quality gauges and fixturing, reliability analysis, problem solving and continuous improvement activities.
• Assists in preparation and updates of manufacturing procedure documentation, and quality procedure documentation.
• Analyzes Non-conformance event and complaint data analysis, investigates to determine root cause, proposes improvements, and maintains CAPA documentation.
• Writes new procedures and work instructions or update the existing documents to drive process improvement.
• Evaluates and monitors manufacturing issues, product concerns, and field complaints to determine opportunities for improving manufacturing and product performance.
• Assists with incoming materials by confirming specifications; conducting visual and measurement tests
• Assists with the equipment calibration and inspection process.
• Identifies opportunities to improve manufacturing processes, e.g., lean techniques.
• Promotes a culture of continuous improvement, reinforces the elimination of process variation and supports business improvement and profitability.
• Assists in internal quality audits and supplier audits
Position Requirements
Bachelor’s degree in Engineering, Science or Quality
• 5 Years experience in quality engineering position at medical device company
• Strong attention to detail
• Highly organized
• Effective communication skills
• Ability to work independently or as a team
Additionally Desired:
• Working knowledge of ISO 13485: 2003, 21 CFR, CMDR, other international regulations
• Proficiency in CAD-Solidworks or ProE

Vapotherm - 23 months ago - save job - copy to clipboard