Npi Quality Project Manager

Johnson & Johnson Johnson & Johnson · Pharma · Ciudad Juarez, Mexico

The NPI Quality Project Manager at Johnson & Johnson is responsible for planning, coordinating, and directing quality assurance programs for new product introductions and existing processes. This role involves collaborating with NPI, operations, and engineering teams on validation strategies, leading quality improvement initiatives using methodologies like Six Sigma and Lean, ensuring compliance with regulations (QSRs, ISO 13485), managing quality costs, and overseeing product quality control and disposition. The position also involves risk assessment, process validation, and ensuring the effectiveness of quality systems in a regulated medical industry environment.

What you'd actually do

  1. Collaborates with NPI and with the operations and engineering departments to develop, conduct and approve validation strategies of products and processes.
  2. Leads or support quality improvement initiatives, such as the characterization of processes and products that leads to continuous improvements / cost.
  3. Revises / analyzes if the current products and processes (including performed actions or decisions) comply with the regulations, such as the QSRs, ISO 13485, etc.
  4. Revises and approves the investigations, bounding, documentation, revision and approval of the non-conformities (NCs), preventive and corrective actions (CAPAs), customer complaints and escalation of quality problems when applies.
  5. Responsible and owner of the risk assessment evaluation including the realization, documentation, revision, maintenance of current risk and documentation of the risk assessment such as FMEA of the process given to changes in the product/process.

Skills

Required

  • Quality Assurance
  • New Product Introduction (NPI)
  • Process Validation
  • Regulatory Compliance (QSRs, ISO 13485)
  • Quality Management Systems
  • Risk Management (FMEA)
  • Six Sigma / Lean methodologies
  • Leadership
  • Project Management
  • Problem Solving

Nice to have

  • Experience in the medical device industry
  • Budget management
  • Auditing

What the JD emphasized

  • validation strategies
  • quality improvement initiatives
  • continuous improvements
  • compliance with the regulations
  • QSRs
  • ISO 13485
  • quality costs
  • product quality
  • process validation
  • risk assessment