Associate Manager, Quality Engineering

## Associate Manager, Quality Engineering Apply:
USA, Texas, Austin:
Full time:
Posted Today:
R0034505##
** Who We Are
**** ABOUT ENOVISTM
** Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement, global talent and innovation, the Company’s extensive range of products, services and integrated technologies fuels active lifestyles in orthopedics and beyond. For more information about Enovis, please visit
** What You'll Do
** At EnovisTM we pay attention to the details. We embrace collaboration with our partners and patients, and take pride in the pursuit of scientific excellence — with the goal of transforming medical technology as we know it.

Because that’s how we change the lives of patients for the better. And that’s how we create better together. Why work at Enovis? See for yourself.

As a key member of the Quality Assurance Team, you will play an integral part in helping Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes.  
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* Job Title:

** Associate Manager, Quality Engineering
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* Reports To:

** Associate Director, Quality Engineering
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* Location:

** Austin, Texas
** Business Unit

Description:

** Quality Assurance  
** Job Title/High-Level

Position Summary:

** The Associate Manager, Quality Engineering provides day-to-day leadership, technical guidance and support to the Quality Engineering team while remaining actively involved in supporting manufacturing operations. This role serves as a key quality partner to Manufacturing and Operations, supporting and leading quality investigations, Material Review Board (MRB) activities, continuous improvement initiatives, and quality system compliance. The Associate Manager also supports the leader of quality with team priorities, employee development, and execution of departmental objectives.

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* Key Responsibilities:

*** Provide day-to-day technical guidance, direction, and support to Quality Engineers and other Quality team members.
* Assist in managing team priorities, resource allocation, employee development, and execution of departmental objectives to ensure business and quality goals are achieved.
* Manage and supervise assigned Quality Engineering personnel, including performance management, coaching, training, development planning, and employee engagement activities.
* Coach and develop team members through regular feedback, technical guidance, and development opportunities.
* Serve as a key Quality partner to Manufacturing and Operations, providing timely support for production and quality-related issues.
* Lead and facilitate risk-based decision making regarding manufacturing deviations, process changes, supplier-related quality issues, and product quality concerns.
* Lead and support Material Review Board (MRB) activities, including evaluation and disposition of nonconforming material.
* Monitor production and quality data, communicate key metrics, identify emerging risks and trends, and escalate significant quality concerns as appropriate.
* Lead root cause and CAPA investigations using structured problem-solving methodologies and ensure corrective actions are implemented and verified for effectiveness.
* Lead or support process and equipment validations, including IQ/OQ/PQ/TMV, and review and approve related protocols, reports, and engineering documentation.
* Lead or support supplier quality activities including supplier investigations, Supplier Corrective Action Requests (SCARs), supplier performance monitoring, supplier transfers, and supplier change management activities.
* Develop and recommend updates to quality standards, procedures, work instructions, and processes.
* Monitor and drive site quality metrics including FPY, NCMRs, CAPA effectiveness, complaint trends, and audit performance. Develop action plans to address adverse trends.
* Support compliance with applicable internal requirements and regulatory standards, including GMP, FDA requirements, and ISO 13485.
* Review trends related to scrap, nonconforming material, process deviations, and device failures to identify systemic quality concerns.
* Partner cross-functionally with Manufacturing, Engineering, and Operations to resolve quality issues and support manufacturing transfers, new product introductions, process changes, and continuous…