Quality Engineer: Design & Manufacturing Quality

Bestlogic Staffing; Bay Shore (NY); On-site; USD 85,000 - 120,000; Full time

Job summary

BestLogic Staffing seeks a Quality Engineer to ensure quality throughout the Product Development Process (PDP) and lifecycle of our products. You will participate in QD&D during design, support sustaining manufacturing, distribution, and post-market surveillance, and drive improvements with robust data analysis.

The role requires collaboration with cross-functional teams, strong root cause analysis, and adherence to ISO, FDA, and other regulatory standards, with a focus on continuous improvement.

Qualifications

• Bachelor's degree in engineering or related field.
• Experience as a Quality Engineer in manufacturing or product development.
• Knowledge of QA methodologies, product development processes, and regulatory standards.
• Certification in quality management systems is a plus.

Responsibilities

• Collaborate with cross-functional teams to support QD&D activities.
• Plan, execute, and monitor QA measures during new product development.
• Lead root cause analysis and implement corrective actions.
• Assure quality during product distribution and post-market surveillance.
• Ensure compliance with ISO, FDA, and other regulations.
• Drive continuous improvement using data analysis and metrics.
• Communicate quality expectations across engineering, manufacturing, and supply chain.

Skills

Quality engineering

Quality assurance

Root cause analysis

Risk management

Communication

Six Sigma

Education

Bachelor's degree in engineering

Tools

MS Office

Statistical software

QMS software

Job description

BestLogic Staffing seeks a Quality Engineer to ensure quality throughout the Product Development Process (PDP) and lifecycle of our products. You will participate in QD&D during design, support sustaining manufacturing, distribution, and post-market surveillance, and drive improvements with robust data analysis.

The role requires collaboration with cross-functional teams, strong root cause analysis, and adherence to ISO, FDA, and other regulatory standards, with a focus on continuous improvement.