Sr Quality Systems Engineer

Johnson & Johnson Johnson & Johnson · Pharma · Santa Clara, CA +1

This role is responsible for the maintenance and continuous improvement of the Quality Management System and Compliance elements, including CAPAs, Quality Manual, and Quality Planning. It involves assisting with the development and implementation of processes, procedures, and corrective actions, ensuring compliance with quality standards and regulatory requirements like ISO 13485 and GMP in a regulated environment.

What you'd actually do

  1. Assist in developing, administering, and maintaining quality system procedures and activities to ensure that processes and products follow applicable quality standards and regulatory requirements through the coordination of the Quality Management System Change Review Forum.
  2. Support and assist with assessment, adoption and integration of Shared Franchise Procedures.
  3. Assist and support for QMS updates to support market expansion into new markets.
  4. Prepare for and participate in quality governance and oversight meetings (e.g. Quality Systems Management Review) as assigned.
  5. Collect, compile, and report monthly quality systems metrics

Skills

Required

  • ISO 13485
  • ISO 14971
  • GMP guidelines
  • FDA regulations
  • quality systems
  • quality engineering
  • risk management
  • communication
  • presentation
  • interpersonal skills

Nice to have

  • Agility Jumps
  • Analytical Reasoning
  • Analytics Dashboards
  • Coaching
  • Collaborating
  • Communication
  • Compliance Management
  • Data Compilation
  • Data Quality
  • Data Savvy
  • Document Management
  • Problem Solving
  • Quality Auditing
  • Quality Control (QC)
  • Quality Management Systems (QMS)
  • Quality Services
  • Quality Standards
  • System Audits
  • Systems Analysis

What the JD emphasized

  • regulated environment
  • ISO 13485
  • 14971
  • GMP guidelines
  • FDA regulations