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Quality Engineer

Job in Leesburg, Loudoun County, Virginia, 22075, USA
Listing for: Valid8 Financial, Inc.
Full Time position
Listed on 2025-12-01
Job specializations:
  • Engineering
    Quality Engineering, Process Engineer
  • Quality Assurance - QA/QC
    Quality Engineering
Job Description & How to Apply Below
Position: Staff Quality Engineer

Looking for a career where your work truly matters? At VB Spine, you’ll be part of a mission-focused team that supports surgeons during life-changing spinal procedures. We’re looking for a Staff Quality Engineer who can thrive in a fast-paced environment, lead complex quality initiatives, and support high-impact programs that drive product excellence and patient safety.

What You’ll Do:
  • Work closely with operations and business functions to ensure product and process quality performance
  • Serve as the Quality representative on cross-functional teams to resolve key quality issues
  • Lead quality initiatives that support compliance to standards and drive process improvements
  • Develop, maintain, and improve internal procedures, SOPs, and work instructions
  • Assess internal and supplier change management activities
  • Apply risk management practices to manufacturing operations
  • Lead internal and supplier non-conformances and ensure timely closure
  • Lead CAPA projects, including investigation, implementation, and closure
  • Act as SME during audits by regulatory agencies, notified bodies, and other authorities
  • Lead process and quality system projects of moderate scope and complexity
  • Disposition non-conforming product within the MRB
  • Maintain KPIs, perform analyses, and interpret trends to drive action
  • Identify and execute supplier part certification opportunities
  • Support creation and maintenance of inspection methods and sampling plans
  • Perform supplier control activities, including on‑site and desktop audits
  • Manage and maintain the Approved Supplier List (ASL)
  • Lead development and improvement of manufacturing processes
  • Lead supplier part approval activities for new products and changes
  • Apply foundational knowledge of manufacturing processes (milling, turning, heat treatment, passivation/cleaning)
  • Execute internal quality deliverables for engineering changes, product transfers, and supplier-initiated changes
  • Lead complex product transfers between manufacturing sites
  • Lead containment and communication activities related to potential product escapes
  • Lead execution and analysis of manufacturing-related complaints and field actions
  • Review, execute, and approve equipment, process, MSA, and software validation protocols/reports
  • Collaborate with Regulatory on creation and revision of IFUs
  • Review and approve quality records
  • Utilize ERP systems for purchasing and manufacturing quality processes
  • Promote Human Factors practices, including identification and mitigation strategies
  • Apply statistical analysis and process control methods for CAPA, management review, and QMS processes
  • Provide training (GMP, onboarding, etc.) and cross-functional support for NPD and process changes
  • Provide subject matter expertise and mentorship to junior Quality team members
What You Bring:
  • Bachelor’s degree required;
    Engineering discipline preferred (Biomedical, Process, Mechanical)
  • Minimum 5 years’ experience in a quality role within a medical device company (or equivalent regulated manufacturing experience)
  • Professional quality certification (MS, CQE, CRE, Six Sigma) highly desirable
  • Knowledge of quality concepts (Risk Management, CAPA, Audits, Statistics)
  • Knowledge of regulatory requirements (ISO 13485, FDA QSR, EU MDR)
  • Experience interacting with regulatory agencies (FDA, MoH, TUV, etc.)
  • Strong investigation and root‑cause analysis skills preferred
  • Process improvement and auditing skills preferred
  • Ability to read engineering drawings/technical specifications preferred
  • Ability to multitask, work independently, and participate in cross-functional teams
  • Project management skills and ability to influence without authority
  • Excellent communication, analytical, problem-solving, and technical writing skills
  • High attention to detail and strong organizational skills
  • Ability to meet physical requirements such as standing, walking, sitting, reaching, and standard vision capabilities
Why VB Spine?

We believe in growing talent from within. At VB Spine, you’ll join a high-performing team, benefit from peer and executive mentorship, and help shape strategy in the dynamic field of medical devices—positioning yourself to influence growth and innovation across the organization.

Compensation:

Pay for this role…

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