Johnson & Johnson Work Values

Daily Duties at Johnson & Johnson:

Conducted internal and supplier audits to assess compliance with ISO 9001 or 13485 requirements. Monitored all CAPAs to ensure that nonconformities were adequately addressed. Responsible for the closure of all nonconforming material reports. Reviewed and approved product complaint investigations. As the Deputy Management Representative, reported on various quality metrics. Created and reviewed specifications, test methods, and sampling plans. Hosted regulatory audits and inspections.

What they like about Johnson & Johnson:

Organizations with strong, centralized leadership are particularly attractive to you. You require a work environment with leadership that aggressively seeks to expand and grow the business and does so in a visible and decisive manner. In general you prefer to work in an environment in which there is a strong link between leadership, its actions, and a strong set of company-wide values.

Tags

Quality Engineer, Supplier Quality Engineer, Quality Supervisor, Documentation Supervisor, Regulatory Compliance, Pharmaceuticals, Medical Devices, In Vitro Diagnostics, Clinical Products, Commercial products, Training, FDA, Health Canada, Notified Bodies, SOPs, Test Methods, Stability Testing, Product Complaints, Calibration, ISO 13485: Lead Auditor, Reliability Engineer, Risk Management, Six Sigma, CAPA, Regulatory Affairs Certified, Nonconforming Product, Quality Auditor, Biomedical Auditor, Internal Audits, Supplier Audits, Validation

Skills

Quality Audits, Corrective and preventive actions, FDA Pharmaceutical and Medical Device Regulations, Providing GMP, QSR, and ISO Training, Risk management, Communicating with all levels of personnel, Conducting management review meetings, Logistics, Product transfer, Supplier Quality Management

These are some of the questions we asked our climbers about their experiences with Johnson & Johnson: