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QA Consultant – GCP Compliance for FDA Audit Preparation

System One
Durham, North Carolina, US
Full-time

Job Title : QA Consultant (GCP Compliance)

Read all the information about this opportunity carefully, then use the application button below to send your CV and application.

Location : Remote with potential travel to company sites as needed.

Hours / Schedule : 20hrs / wk for first few months, then transitioning to 40hours / wk as time goes on.

Compensation : Open to discuss, depending on experience.

Contract Length : 3-6 months, with potential for extension based on project needs.

Overview :

We are seeking an experienced QA Consultant to assist a biotech company in preparing for an FDA audit with a strong focus on Good Clinical Practice (GCP) compliance.

The ideal candidate will have a deep understanding of GCP regulations and extensive experience guiding companies through FDA submission readiness, ensuring documentation, processes, and practices meet all regulatory requirements.

Key Responsibilities :

  • Reviewing GCP operations and documentation to support regulatory filing (NDA submission).
  • Supporting inspection readiness by assessing compliance with site, sponsor and provider (eclinical companies, biorepositories, clinical labs).
  • Assess current QA processes and documentation for GCP compliance.
  • Identify gaps and provide actionable recommendations to align with FDA requirements.
  • Develop and implement SOPs, training programs, and corrective actions as needed.
  • Conduct mock audits and prepare teams for potential audit scenarios.
  • Review clinical trial data, monitoring processes, and vendor qualifications for adherence to GCP.
  • Support the company in compiling and organizing audit documentation for FDA submission.
  • Provide guidance during the audit process and help address any findings or concerns.

Qualifications :

  • Bachelor's degree in Life Sciences or related field; advanced degree preferred.
  • Minimum of 5 years of experience in QA with a focus on GCP and FDA audits.
  • Proven track record of preparing small biotech or pharma companies for successful FDA inspections.
  • Proven examples of gap assessments performed and remediated in advance of filing and inspection.
  • Strong understanding of FDA regulations, ICH guidelines, and GCP principles.
  • Excellent communication skills and the ability to work effectively with cross-functional teams.

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2 hours ago
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