Talent.com
Quality Engineer II

Quality Engineer II

Alphatec SpineCarlsbad, CA, US
job_description.job_card.variable_days_ago
serp_jobs.job_preview.job_type
  • serp_jobs.job_card.full_time
job_description.job_card.job_description

Mechanical Quality Engineer

Mechanical Quality Engineer supporting new product development. Develop, improve, and implement quality methods and systems, working on cross functional teams in a regulated environment to ensure the safety, reliability and efficacy of products and processes.

Essential Duties And Responsibilities

  • Support New Product Development as primary QE for mechanical implants and instruments. Manage multiple concurrent major and minor projects.
  • Support Design Controls to ensure efficient, effective, and compliant new product launches.
  • Support the qualification of legal manufacturers (OEM) for distributed products.
  • Lead Material Review Board (MRB), own Non-Conformance (NC) development and resolution, lead reworks and deviations, participate in Supplier Review Board (SRB).
  • Develop inspection plans and custom gauging based upon required measurement and tolerances.
  • Support Change Order review for drawings, considering Design for Manufacturing (DFM) and Design for Inspection (DFI).
  • Act as liaison between supplier and company for quality related concerns or issues. Technical interface with contract manufacturers.
  • Support cleaning and sterilization validations of implantable devices; basic understanding of tests such as bioburden, BET, and dose audit testing.
  • Support validation (IQ, OQ, and PQ) development and execution internally and at suppliers.
  • Apply statistical techniques to analyze manufacturing processes and recommend appropriate process controls.
  • Support Risk Management efforts in accordance with ISO 14971; conduct preliminary risk assessments for projects. Support Failure Mode and Effects Analysis (FMEA) for designs and processes.
  • Support Field Retrieval Assessment (FRA) and Health Hazard Evaluation (HHE) as needed.
  • Support MDSAP, FDA, ISO, and other regulatory audits.
  • Apply external standards and guidance documents to project / product specific application.
  • Own Supplier Corrective Actions (SCARs) and Corrective and Preventive Actions (CAPAs).
  • Lead supplier part qualification for new products including process qualifications (PQs), GR&R, first articles, and process development.
serp_jobs.job_alerts.create_a_job

Quality Engineer Ii • Carlsbad, CA, US