Process Quality Engineer - Drive Process Improvement

8722-DePuy International Limited Legal Entity; Churwell; On-site; GBP 45,000 - 65,000; Full time

Benefits offered by this job

Competitive compensation

Comprehensive benefits package

Learning & development opportunities

Job summary

Johnson & Johnson is seeking a Process Quality Engineer in Leeds to apply quality engineering tools across the product lifecycle. You will support process characterization, verification, validation, and CAPA management while ensuring compliance with global standards and audits.

Strong data analysis and cross‑functional collaboration are essential. The role emphasizes risk management, investigation of non-conformances, and ongoing process improvement in a manufacturing setting.

Qualifications

• A degree or equivalent experience in engineering or related technical field is required.
• Experience in manufacturing or operations environments is preferred.
• Knowledge of FDA and ISO standards and risk management is expected.

Responsibilities

• Support quality improvement initiatives and drive continuous improvement.
• Review PDCA, Six Sigma, Kaizen and Lean techniques for effectiveness.
• Ensure compliance with QSRs, ISO13485 and global standards.
• Partner with R&D and cross‑functional teams on design controls and risk management.
• Own quality metrics and support investigations, CAPAs, and customer complaints.

Skills

Customer Centricity

Data Savvy

Document Management

Execution Focus

Good Automated Manufacturing Practice

Issue Escalation

Lean Supply Chain Management

Process Control

Process Improvements

Quality Control Testing

Quality Standards

Quality Systems Documentation

STEM Application

Supervision

Supply Planning

Technologically Savvy

Education

Degree in Engineering or related technical field

Job description

Johnson & Johnson is seeking a Process Quality Engineer in Leeds to apply quality engineering tools across the product lifecycle. You will support process characterization, verification, validation, and CAPA management while ensuring compliance with global standards and audits.

Strong data analysis and cross‑functional collaboration are essential. The role emphasizes risk management, investigation of non-conformances, and ongoing process improvement in a manufacturing setting.