What are the responsibilities and job description for the Manufacturing Quality Engineer position at United Pharma?
Manufacturing Quality Engineer Medical Device
Location: NY Onsite
Experience: 5 plus Years
About the Role:
We are seeking a mid-level Manufacturing Quality Engineer to support the design, installation, testing, and startup of industrial control systems within a medical device environment. This role will focus on ensuring quality, reliability, and compliance of manufacturing and test equipment used in production.
Key Responsibilities:
Provide quality engineering support for manufacturing and production equipment
Assist in design, installation, testing, and startup of industrial control systems
Ensure compliance with FDA regulations and medical device quality standards
Support validation and testing activities for manufacturing processes and equipment
Collaborate with cross functional teams including Engineering, Quality, and Production
Identify and resolve quality issues using root cause analysis and corrective actions
Drive continuous improvement initiatives to enhance product quality and process efficiency
Key Skills:
Manufacturing Quality Engineering
Medical Device Industry Experience
Industrial Control Systems
Process Validation and Testing
Root Cause Analysis and CAPA
FDA and Quality Compliance
Required Qualifications:
Bachelor’s degree in Mechanical, Electrical, or Software Engineering
5 plus years of experience in manufacturing and quality engineering
Experience supporting testing and production equipment
Strong background in medical device industry
Knowledge of quality systems and regulatory standards
Preferred:
Experience with automation or control systems
Familiarity with validation and testing methodologies
Lean or Six Sigma certification