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Senior Manager Quality Operations

Job in California, Moniteau County, Missouri, 65018, USA
Listing for: LDI Search LTD.
Full Time position
Listed on 2026-03-01
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
  • Management
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Location: California

Senior Manager Quality Operation (Medical Devices)

A global, innovation-driven medical technology organization is seeking an experienced Senior Manager Quality Operation (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
Required Qualifications
  • 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
Preferred Qualifications
  • 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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Position Requirements
10+ Years work experience
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