Director Supplier Quality
Job in
Lebanon, Wilson County, Tennessee, 37090, USA
Listed on 2026-06-02
Listing for:
Permobil, Inc.
Full Time
position Listed on 2026-06-02
Job specializations:
-
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist -
Engineering
Quality Engineering, Regulatory Compliance Specialist
Job Description & How to Apply Below
Director Supplier Quality
Lebanon, TN
Key Tasks- Develop and maintain a supplier quality system that ensures that Permobil is fully compliant to rules and regulations such as FDA and EU MDD and ensures high quality products for our users.
- Develop and maintain supplier quality processes for new projects and change management in alignment with Regional QMS procedures.
- Be the link between Regional Quality organizations, Production Units and BF Supply Chain for supplier quality and compliance related matters.
- Support to the Regions with supplier quality activity and QMS requirements such as Management Review, CAPA, Internal Audits.
- Define Supplier Quality metrics in alignment with QMS.
- Develop and maintain supplier quality assurance and audit programs.
- Develop and execute strategy for Responsible Sourcing in alignment with Permobil Sustainability initiatives.
- Lead supplier and product/process audits program.
- Develop and maintain training and development material and plans for employees and suppliers.
- Communication of Permobil supplier quality requirements to suppliers.
- Lead re-evaluation process of the supplier base.
You are passionate, innovative, and ambitious. You want to make a difference for others and feel fulfilled when you can see the link between the work you do and positive improvements in the lives of others. You search out opportunities and are prepared to go off the beaten track to chase your dreams. You don't follow the herd – you find new ways of working and go where you see potential to make your mark.
You are a pioneer, a revolutionary, a game-changer and you are who we're looking for.
- University Degree (or similar) and/or
- Equivalent experience in related fields such as quality engineering, production engineering, supply chain, product development, project management
- Preferably has been certified to audit
- Quality Management Systems such as ISO 9001 or equivalent
- ISO 13485 Quality System for Medical Device
- Regulatory requirement CFR 820 issued by Food and Drug Administration in USA.
- Regulatory requirement EU Regulation 2017/745 issued by the European Union
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