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. Key Responsibilities 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. Required Qualifications 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. Preferred Qualifications Experience with Veeva Quality applications. Experience using SharePoint for document management and collaboration. Experience with electronic Quality Management Systems (eQMS) and quality metrics reporting. #J-18808-Ljbffr United Pharma Technologies Inc