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Job description
The Quality Engineer is responsible for supporting the effectiveness of the Quality Management System (QMS) and to ensure compliance of QMS activities to ISO13485:2016. Partner with management team to ensure adherence to the QMS. Provide consistent product and process support for shop floor manufacturing to ensure maximized uptime and high product quality is achieved.
ESSENTIAL FUNCTIONS
Supports the maintenance of the QMS ensuring its continuing suitability, adequacy and effectiveness
Shop floor support for troubleshooting, root cause analysis, support production uptime with engineering
Red Cart Process and Gemba Walk
Corrective and Preventive Action System (CAPA) ownership
Support the Equipment Qualification and Validation Process (including IQ, OQ and PQ, etc)
Works with Engineering to draft and execute protocols
Nonconforming Material System (NCMR) ownership and leads the MRB process where applicable
Performs First Article Inspections (FAI) with QC Personnel
Where applicable, creates and executes Measurement System Analysis (Gage R&R)
Support day to day operations to drive Key Process Indicator (KPI) improvements and business objectives
Supports the Approved Supplier List (ASL) Evaluations, Reporting and Feedback
Creates and edits Standard Operating Procedures, Work Instructions and Forms
Provides input to FMEAs / Risk Management
Performs Product Quality Inspections as needed
Performs Measuring and Monitoring Equipment Calibration as needed
Performs Training as needed
Perform other relevant duties as assigned by supervisor
SPECIFIC JOB KNOWLEDGE, SKILL AND ABILITY
The individual must possess the following knowledge, skills and abilities and be able to explain and demonstrate that he or she can perform the essential functions of the job, with or without reasonable accommodation.
Full understanding of a QMS and conformance to ISO13485
Nonconforming materials, calibration, corrective and preventive actions, root cause analysis, etc
Experience in medical component or medical device manufacturing required
Proficient in use of metrology (hand devices, vision systems, microscopes, non-contact devices, profilometer)
Basic proficiency in reading drawings, GD&T and blueprints
Ability to read, listen and communicate effectively in English, both verbally and in writing
Experience in customer, registrar or FDA audits/inspections a plus
Ability to navigate a computer ERP system, in certain modules, and perform data entry, data retrieval
Computer Skills – Microsoft Office Suite: Word, Excel, Powerpoint, Visio required (QMS software and Minitab experience a plus)
Willingness to continually work beyond scope of essential duties in order to assist whenever and wherever needed to ensure company needs are met
QUALIFICATION STANDARDS
Experience:
3 to 5 years of related experience in quality engineering in medical device or medical components
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Worksite address
raynham, MA, 02767, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.