Sr Quality Engineer

Senior Quality Engineer

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• Develop, implement, and maintain Quality Management Systems (QMS) in compliance with FDA, EMA, ICH guidelines, and other regulatory requirements.
• Ensure all processes and products comply with applicable regulatory standards, including cGMP.
• Lead continuous improvement initiatives to enhance product quality, efficiency, and compliance.
• Oversee validation activities, including equipment, process, and cleaning validations, ensuring compliance with industry standards.
• Conduct thorough investigations into quality issues, perform root cause analysis, and implement corrective and preventive actions (CAPA).
• Plan and conduct internal audits, support external regulatory inspections, and manage responses to audit findings.
• Evaluate and qualify suppliers, conduct supplier audits, and ensure supplier compliance with quality standards.
• Maintain accurate and comprehensive quality documentation, including SOPs, batch records, and validation protocols.
• Mentor and develop junior quality engineers and quality assurance staff, fostering a culture of continuous improvement and quality excellence.
• Perform risk assessments and implement risk mitigation strategies related to product quality and regulatory compliance.
• Work closely with cross-functional teams, including R&D, manufacturing, and regulatory affairs, to ensure quality considerations are integrated into all phases of product development and production.

• 7-10 years of experience in Quality Assurance within a FDA/GMP environment (pharmaceutical or medical device industry required).
• Bachelor's degree in a scientific field (Life Sciences, Biotechnology, or equivalent) is required.
• Proficiency in quality management software, statistical analysis tools, and methodologies such as Six Sigma, Lean.
• Strong understanding of Quality Management Systems.
• Previous experience with hosting client audits and/or regulatory inspections.
• Excellent communication skills.

• Certified Quality Engineer (CQE) or Certified Quality Auditor certification preferred.
• Experience with electronic Quality and Training Management Systems.

Mid-Senior level

Contract

Quality Assurance

Pharmaceutical Manufacturing

St Charles, MO

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