More jobs:
Site Quality Leader
Job in
California, Moniteau County, Missouri, 65018, USA
Listed on 2026-03-01
Listing for:
LDI Search LTD.
Full Time
position Listed on 2026-03-01
Job specializations:
-
Quality Assurance - QA/QC
Quality Engineering
Job Description & How to Apply Below
Site Quality Leader (Medical Devices) The Opportunity
A global, innovation-driven medical technology organization is seeking an experienced Site Quality Leader to oversee Quality operations at a high-profile manufacturing facility in Southern California. This role is a key member of the Site Leadership Team and offers the opportunity to shape quality strategy, strengthen compliance, and elevate quality culture across the organization.
This position is ideal for a senior Quality professional who thrives in regulated environments and enjoys leading teams, influencing stakeholders, and driving continuous improvement from product development through post-market performance.
Your Impact- Serve as the Quality Management Representative for the manufacturing site, providing strategic and technical leadership across end-to-end product and process quality for regulated medical devices
- Lead and develop a team of Quality Engineers and supervisors, with accountability for performance management, goal setting, and talent development
- Drive effective interpretation of quality and performance data to resolve nonconformances, meet customer and regulatory requirements, and support business objectives
- Proactively identify and lead quality improvement initiatives to enhance product capability, process robustness, and operational efficiency
- Ensure ongoing compliance with applicable global quality regulations and standards, including U.S. and international medical device requirements
- Provide guidance to cross-functional teams on quality strategy, risk management, process validation, and continuous improvement initiatives
- Act as an influential peer leader on the Site Leadership Team, strengthening compliance, quality culture, predictive quality practices, and data-driven decision-making
- Bachelor’s degree or higher
- Minimum 10 years of experience in a Quality function within Medical Devices, Pharmaceuticals, or Combination Products
- At least 3 years of people management experience
, demonstrating effective leadership, compliance excellence, and risk mitigation
- ASQ Certified Quality Engineer (CQE), Certified Manager of Quality/Organizational Excellence (CMQ/OE), and/or Six Sigma Black Belt
- Demonstrated experience with:
- Regulatory authority interactions and audits
- Quality engineering, process validation, and nonconforming material control
- Risk management, field actions, recalls, and post-market surveillance
- Continuous process and product improvement initiatives
- Proven ability to influence across functions and levels, including executive leadership
- Strong written and verbal communication skills, with the ability to present clear, fact-based insights
- Decisive, results-oriented leadership style with strong problem-solving and prioritization skills
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