Director of Quality Systems - Mesa, United States - Biolab Holdings, Inc

Biolab Holdings, Inc
Biolab Holdings, Inc
Verified Company
Mesa, United States

3 weeks ago

Mark Lane

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Mark Lane

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Description

Job Summary:


Responsibilities:


  • Develop and maintain comprehensive quality systems and procedures to ensure compliance with regulatory standards, including AATB requirements.
  • Lead process improvement initiatives to enhance efficiency, effectiveness, and quality throughout the organization.
  • Oversee document control processes, ensuring proper documentation, review, and approval of qualityrelated documents.
  • Manage the Corrective and Preventive Action (CAPA) program, including investigation, root cause analysis, implementation of corrective actions, and effectiveness monitoring.
  • Investigate and manage deviations from established processes, ensuring timely resolution and prevention of recurrence.
  • Collaborate with crossfunctional teams to implement qualityrelated initiatives and drive continuous improvement.
  • Conduct internal audits and assessments to evaluate compliance with quality systems and regulatory requirements.
  • Prepare for and participate in regulatory inspections and audits, including interactions with regulatory agencies.
  • Provide leadership, guidance, and training to quality systems personnel to ensure competence and compliance with quality standards.
  • Stay informed of industry trends, best practices, and regulatory updates related to tissue banking and birth tissue manufacturing.

Qualifications:


  • Bachelor's degree in a relevant field (e.g., Biology, Chemistry, Engineering).
  • Minimum of 8 years of progressive experience in quality management, with specific expertise in process improvement, document control, CAPAs, and deviations within a regulated industry (preferably tissue banking or medical device manufacturing).
  • Indepth knowledge of AATB standards and regulations applicable to tissue banking operations.
  • Proven track record of implementing and managing quality systems, process improvements, and compliance initiatives.
  • Strong analytical skills with the ability to identify root causes and drive effective corrective actions.
  • Excellent communication, leadership, and interpersonal skills, with the ability to collaborate across functions and levels of the organization.
  • Experience in leading internal audits, regulatory inspections, and interactions with regulatory agencies (FDA, CBER, etc.).
  • Certified Quality Auditor (CQA) or similar certification is a plus.

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