Sr. Quality Engineer

Actalent-posted 27 days ago
$42 - $72/Yr
Full-time • Mid Level
Onsite • Saint Louis, MO
1,001-5,000 employees
Administrative and Support Services
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We are seeking a highly experienced and motivated Senior Quality Engineer to join our pharmaceutical manufacturing team. The ideal candidate will have a strong background in quality assurance within the pharmaceutical industry, with a comprehensive understanding of regulatory requirements, quality systems, and process improvements. This role is critical to ensuring compliance with all relevant regulations and standards, leading quality initiatives, and supporting the manufacturing of pharmaceutical products.

  • 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.
  • Medical, dental & vision
  • Critical Illness, Accident, and Hospital
  • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
  • Life Insurance (Voluntary Life & AD&D for the employee and dependents)
  • Short and long-term disability
  • Health Spending Account (HSA)
  • Transportation benefits
  • Employee Assistance Program
  • Time Off/Leave (PTO, Vacation or Sick Leave)
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