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QA Compliance, Manager

Granules

Job Description

Job Description

Description:

 

JOB DUTIES & RESPONSIBILITIES

  • Lead and guide cGMP Compliance efforts at the Chantilly site, ensuring alignment with applicable regulations.
  • Possess expert knowledge of 21CFR, ICH, and USP to effectively interpret and apply regulations in addressing cGMP Operations-related queries at the Chantilly site.
  • Serve as the site’s Quality representative during FDA inspections.
  • Assist in inspections by external regulators and business partners.
  • Conduct Compliance GAP analyses, providing recommendations for gap closure, implementation, and follow-up effectiveness checks.
  • Develop and execute site-wide remediation and improvement plans based on Quality metrics assessments.
  • Maintain and analyze Quality metrics for the site to ensure continued Compliance.
  • Build and manage systems, processes, and cross-functional teams to oversee Compliance at the site.
  • Manage and support direct reports by establishing clear expectations and resolving conflicts.
  • Ensure adherence to company procedures and resolve deviations from procedures or cGMP requirements promptly.
  • Collaborate with various departments on quality issues, audits, and special projects.
  • Offer guidance to manufacturing teams on Quality cGMP issues, ensuring compliance with applicable standards and regulations in coordination with the Site QA team.
  • Provide technical expertise in deviations, CAPA, Root Cause Assessments, cGMP compliance, and data trending.
  • Review and approve protocols, SOPs, and investigations.
  • Oversee and supervise the collection of data for product review.
  • Prepare and review documentation required for regulatory submissions, as needed.
  • Participate in the Quality Task Force and contribute to the development and review of company standard operating procedures.
  • Ensure the site stays up to date with all changes to applicable compendia, regulations, and guidance.
Requirements:

Responsibility includes training and developing direct reports to keep abreast of current technology as it relates to cGMP Compliance. 

Vacancy posted 2 days ago
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