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Confidential

Quality Assurance & Compliance Manager

Confidential, North Atlanta

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“Applicants must be legally authorized to work in the United States without the need for sponsorship now or in the future.”


Quality Assurance & Compliance Manager (Manufacturing Operations)


We are seeking a seasoned Quality Assurance and Compliance Manager to lead quality operations at a high-volume manufacturing facility in the greater Northeast Atlanta region. This role is responsible for overseeing all aspects of the site’s quality systems and compliance programs, ensuring that products consistently meet regulatory standards, internal specifications, and customer expectations.


The ideal candidate will bring strong leadership, strategic thinking, and a passion for driving continuous improvement in a regulated manufacturing environment.


Key Responsibilities

  • Lead, mentor, and develop the QA team, fostering a high-performance culture.
  • Align quality objectives with broader business goals and regulatory expectations.
  • Serve as a key member of the site leadership team, influencing cross-functional decision-making.
  • Manage investigations, deviations, CAPAs, and change control processes.
  • Oversee site procedures and annual product reviews.
  • Lead internal audit programs and act as site contact for customer and regulatory inspections.
  • Ensure audit readiness and sustainable corrective actions.
  • Ensure ongoing compliance with FDA, GMP, ISO, and other applicable standards.
  • Monitor/report Quality KPIs and present performance to senior leadership.
  • Oversee calibration, training, and complaint handling programs.
  • Champion Lean/Six Sigma initiatives to reduce risk and enhance efficiency.


Qualifications

  • Bachelor’s degree in chemistry, Engineering, Life Sciences, or related field (Master’s preferred).
  • 6–8+ years of progressive QA experience within regulated manufacturing (OTC, personal care, pharma, cosmetics).
  • 3+ years in a leadership role managing quality teams and systems.
  • Knowledge of FDA regulations, GMP, ISO standards, and electronic QMS platforms.
  • Proven success leading audits, CAPA programs, and cross-functional initiatives.
  • Excellent communication, analytical, and problem-solving skills.
  • Auditor certification (ASQ CQA, ISO Lead Auditor) a plus.


Additional Information

  • Travel may be required for corporate meetings, audits, or training (up to 10–15%).
  • Relocation assistance may be available.