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Quality Engineer II

Job in California, Moniteau County, Missouri, 65018, USA
Listing for: AAOE - American Alliance of Orthopaedic Executives
Full Time position
Listed on 2026-06-07
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
  • Engineering
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 85000 - 118000 USD Yearly USD 85000.00 118000.00 YEAR
Job Description & How to Apply Below
Location: California

Position Title: Quality Engineer II

Location: Irvine

Position Type: Full time

Description:

Why Orthofix?

Guided by our organizational values Take Ownership |
Innovate Boldly |
Win Together we collaborate closely with world‑class surgeons and other partners to improve people’s quality of life. At Orthofix, we want team members who build relationships and share knowledge, challenge the status quo, and deliver results every day to help us achieve our vision to be the unrivaled partner in Med Tech.

Our global team of over 1,600 employees brings to market highly innovative, cost‑effective, and user‑friendly medical technologies that heal musculoskeletal pathologies for patients and the healthcare professionals who treat them. Looking to change people’s lives? Look no further.

JOB PURPOSE

The position is responsible for performing Quality Engineering activities related to product development and existing product support. The Quality Engineer II approves Quality System documentation, participates in cross functional development teams to develop and release new products, participates/lead cross functional improvement projects and CAPAs, and provides technical support to the QC and calibration departments.

ESSENTIAL FUNCTIONS AND RESPONSIBILITIES

The following are the essential functions of this position. This position may be responsible for performing additional duties and tasks as needed and assigned.

  • Lead cross functional project teams as needed to accomplish quality objectives.
  • Review and approve Quality System documentation in compliance with Sea Spine’s procedures, cGMP requirements and statutory requirements (US FDA, ISO, MDD and MDR) including protocols, technical reports, validation/quality plans, standard operating procedures, risk analysis, design control documents, drawings, and specifications.
  • Facilitate the launching of new or improved products, and the transfer of technology from development to commercialization from a Quality perspective.
  • Develop Design History File deliverables to support timely product launches while ensuring compliance with Quality System and Design Controls principles.
  • Lead Risk Management activities and ensures that appropriate Risk Management tools (AFMEA/DFMEA/PFMEA) are utilized and consistent with applicable regulatory standards.
  • Review outputs of Risk Analyses and lead cross‑functional efforts to identify appropriate risk mitigation activities.
  • Support sustaining activities, Quality Control and Calibration department:
  • Develops and maintains inspection plans using appropriate methodologies to ensure products meet specification and are safe/effective for use.
  • Facilitate MRB activities as assigned by QA management.
  • Support Calibration and Preventive Maintenance activities.
  • Conduct Out of Tolerance investigations.
  • Develop statistically based sampling plans for in‑process inspection, final testing, and validations.
  • Interface with contract manufacturers to develop inspection techniques and support non‑conformance investigations.
  • Use quality engineering tools for problem solving (e.g. DMAIC, SPC, DOE).
  • Identify and implement opportunities for continuous improvement. Interact and coordinate activities with other departments, external vendors, and customers. Assist or lead in the prompt implementation of Quality related projects including:
  • Non‑Conformance resolution, Complaint Investigation and Corrective & Preventative Action(s) (CAPA), Process Validations.
  • Development and implementation of new and updated Quality System procedures for ISO/QSR compliance.
  • Create/support in‑house and supplier process validations using IQ, OQ, PQ methodology including cleaning, water system, sterilization, and software validations.
  • Prepare information for Quality Management Reviews and Operational Reviews such as Trend charts, Pareto Analysis, etc., as required.
  • Participate in FDA inspections, ISO Certification and Surveillance audits and customer audits.

MINIMUM QUALIFICATIONS

The requirements listed below are representative of the education, knowledge, skill and/or ability required for this position.

Education/

Certifications:

  • Bachelor's degree in engineering, Science, or related field

Experience Skills, Knowledge…

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