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CorDx

Global rapid testing & point-of-care diagnostics

Quality Assurance Manager

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeNo salary listed

About the Job

Requirements

  • A bachelor's or master's degree in Biotechnology, Microbiology, Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field.
  • At least 7 years of quality assurance experience in biotech, pharmaceutical, or medical device manufacturing.
  • At least 3 years in a managerial or leadership role overseeing QA teams.
  • Strong knowledge of U.S. FDA, ISO 13485, and other regulatory standards.
  • Experience with QA audits, inspections, CAPA investigations, and risk management.
  • Proficiency with QMS software and documentation control systems.
  • Strong analytical and problem-solving skills, with a data-driven approach to decision-making.
  • Leadership, communication, and cross-functional collaboration skills.

Responsibilities

  • Develop, implement, and maintain Quality Management Systems in accordance with U.S. FDA, ISO 13485, and applicable regulations.
  • Lead internal and external audits, regulatory inspections, and corrective action plans.
  • Oversee batch record reviews, deviations, non-conformance reports, and change controls to maintain product quality and integrity.
  • Develop and enforce Standard Operating Procedures and best practices to ensure consistent quality across manufacturing operations.
  • Collaborate with research and development, production, and regulatory affairs teams to ensure new products and processes meet quality standards.
  • Monitor and analyze quality metrics and key performance indicators to drive continuous improvement initiatives.
  • Ensure adherence to Good Documentation Practices and data integrity policies.
  • Lead, mentor, and develop the QA team, fostering a culture of quality, compliance, and continuous improvement.
  • Train manufacturing and quality teams on quality systems and root cause analysis methodologies.
  • Serve as the primary point of contact for quality-related issues and escalations.
  • Identify quality risks and implement proactive mitigation strategies.
  • Lead investigations and root cause analyses for product defects, deviations, and non-conformances.
  • Drive Lean, Six Sigma, or other process improvement initiatives to enhance efficiency and reduce waste.
  • Stay updated on industry trends, new regulations, and technological advancements in medical device in vitro diagnostics quality assurance.

About the Company

CorDx

Global rapid testing & point-of-care diagnostics

CorDx is a multinational biotech organization that provides rapid testing and point-of-care diagnostic devices. Its products are designed to quickly detect infectious diseases (like COVID-19), pregnancy, drugs of abuse, biomarkers, and other health indicators directly at the patient’s side. The devices work by offering fast diagnostic tests and wearable or handheld systems that deliver results on-site, often supported by data science and artificial intelligence to improve accuracy and capture health data. CorDx differentiates itself from competitors through its global reach (2,100+ employees in over 100 countries), scale, and its emphasis on integrating AI and data-driven insights to enhance diagnostic solutions. The company aims to help answer critical health questions by delivering practical, accessible diagnostics and moving toward personalized healthcare.

Company size
51-200
Company stage
Not listed
Total funding
Not listed
Headquarters
Atlanta, GA
Founded
2006

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