Quality Engineer

Position Overview

This position is responsible for supporting Quality processes and systems compliant to FDA regulations and ISO requirements related to the sale, manufacture, service and distribution of Hearing Instruments and related accessories.

(Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)

• Develop and maintain quality system related procedures.
• Develop and execute training, including competence assessment, for quality-related processes and procedures.
• Create, review and approve Engineering and Manufacturing Change Orders.
• Work cross-functionally to conduct root cause investigation, action planning and verification of effectiveness for CAPA.
• Work with manufacturing, supply chain, engineering, and others to solve internal and external supplier quality issues; investigate non-conforming product and recommend disposition.
• Design, supervise, and perform quality methods such as failure mode effects analysis and statistical process control.
• Establish and maintain systems/methods to monitor incoming, in-process and shipped product quality to ensure safety and performance, identify trends and drive improvements.
• Communicate with local, global and corporate functions and customers, as needed, to resolve system and product quality issues, including customer complaints.
• Drive Quality Planning Process including FMEA (Risk Management), Control Plan and Process Audit, etc.
• Establish and maintain inspection procedures based on the material/product specifications and customer requirements.

• Strong verbal and written communication skills
• Problem solving skills
• Detail oriented
• Root cause analysis
• Risk assessments
• Excellent organizational skills to manage multiple priorities
• Self-directed
• Drive continuous improvement throughout the organization

Required Education
:
Bachelor’s Degree in Engineering or equivalent experience.

• 2+ years related work experience: (Quality Engineering, Quality Control, Quality Improvement Projects, Root Cause Analysis, CAPA) preferred.
• Experience in Medical Device Manufacturing, ISO 13485, highly preferred.

Manufacturing facility and office environment.

Sitting, standing, lifting, bending, reaching, no more than 20 lbs.

Full-time position (Monday-Friday).