Quality Consultant

We are seeking a Mid-Level Quality Consultant with strong experience in the biopharmaceutical/pharmaceutical industry to support Quality Systems and GMP operations. The ideal candidate will have hands‑on experience managing quality records, supporting supplier quality activities, and driving continuous improvement initiatives within a commercial GMP environment.

• Author, manage, and close deviations, change controls, and quality records.
• Coordinate and support data transfer activities across quality systems.
• Generate, monitor, and analyze KPIs, quality metrics, and trend reports.
• Maintain quality documentation and records within electronic Quality Management Systems (eQMS).
• Collaborate with cross‑functional teams to support Quality Systems and continuous improvement initiatives.
• Ensure compliance with GMP regulations, company procedures, and quality standards.
• Support supplier quality activities and documentation as needed.

• Bachelor's degree in a Life Sciences, Engineering, or related discipline.
• 5+ years of Quality experience in the biopharmaceutical or pharmaceutical industry.
• Strong experience managing deviations, change controls, and quality documentation.
• Experience supporting supplier quality activities.
• Solid understanding of commercial GMP manufacturing environments.
• Excellent analytical, communication, and organizational skills.

• Experience with Veeva Quality applications.
• Experience using SharePoint for document management and collaboration.
• Experience with electronic Quality Management Systems (eQMS) and quality metrics reporting.