Quality Engineer

Our client, a Global Leader in the Medical Device Industry has an immediate opening for a Quality Engineer for a 12 Month + Contract Opportunity.  Our client offers results-driven people a place where they can make a difference - every day!  You will also have the opportunity to work with other like-minded, self-directed and detail oriented Top Talents in an extremely collaborative and professional environment. 

Key Responsibilities:

• Developing and implementing methods and procedures for process control, process improvement, testing, and inspection to ensure product quality.
• Designing and installing sophisticated testing equipment and performing product testing and analysis to validate functionality and minimize defects.
• Analyzing reports and defective products to identify trends, root causes, and recommending corrective actions.
• Collaborating with supplier representatives to resolve quality issues, ensuring effective corrective actions are implemented, and contributing to supplier quality improvement initiatives.
• Participating in validation activities to ensure compliance with industry standards and regulatory requirements.
• Supporting cross-functional teams in identifying and mitigating quality risks throughout the product lifecycle.
• Maintaining detailed documentation of quality procedures, findings, and improvements to support audit readiness and continuous improvement.

Qualifications: 

• Degree required (Engineering or a related technical field preferred).
• Minimum 5 years of experience in manufacturing environment.
• Strong analytical and problem-solving skills with the ability to identify root causes and implement effective solutions.
• Excellent written and verbal communication skills for reporting findings and collaborating with cross-functional teams.
• Ability to manage multiple tasks and prioritize in a fast-paced, team-oriented environment.
• Knowledge of quality systems and regulatory standards (e.g., ISO 13485, FDA 21 CFR Part 820).
• PPAP (Production Part Approval Process) experience is preferred.
• Experience working with medical devices or in a regulated manufacturing environment is a plus.
• Familiarity with tools such as FMEA, CAPA, and statistical process control is preferred.