Quality Systems Supervisor

Johnson & Johnson Johnson & Johnson · Pharma · Grecia, Costa Rica

Johnson & Johnson is seeking a Quality Systems Supervisor in Grecia, Costa Rica, to provide quality engineering guidance and support for compliance with the company-wide quality management system. This role involves collaborating with business partners on Quality System Standardization, assisting with procedure creation, monitoring QMS metrics, managing investigations, and providing training. The supervisor will also facilitate product issue assessment, support audits, and ensure compliance with relevant regulations and standards.

What you'd actually do

  1. The Quality Systems Supervisor will serve as a Quality Systems subject matter expert, track and report action plan status/ completion as relates to quality systems improvement efforts.
  2. As needed, assist with creation and modification of Quality System procedures, work instructions and related documentation.
  3. Monitors and reports Quality Management System metrics.
  4. Works on complex investigations and coordinates technical teams and leads cross functional teams to ensure sound experimental design, effective data analysis, identification, implementation, verification and validation of CAPA, Non-Conformance, and subsequent closure of investigations.
  5. Responsible for conducting training in Quality Systems Management principles to business partners

Skills

Required

  • Bachelor's Degree or Equivalent
  • 2-4 years Quality Systems, Quality Engineering, Quality Assurance, or other technical work experience
  • Minimum of 2 years’ experience in an FDA regulated industry
  • Working knowledge of 21 CFR Part 820, 21 CFR 806, ISO 13485, ISO 9001
  • Technical knowledge and experience to work effectively with others in diverse areas of business
  • Ability to effectively prioritize and manage multiple activities and responsibilities
  • Outstanding business and technical communication skills (verbal, written, presentation)

Nice to have

  • Experience using MS Project
  • Project Management Certification
  • familiarity with ISO 14971
  • Proficiency with quality-related applications

What the JD emphasized

  • FDA regulated industry
  • 21 CFR Part 820
  • 21 CFR 806
  • ISO 13485
  • ISO 9001