QA Compliance Specialist

Status: Accepting Candidates About the role Support QA and manufacturing operations by ensuring compliance with GMP, FDA, and ISO requirements through batch record review, product release, and on-the-floor quality support. Key Responsibilities Review and approve batch records, supplemental logs, and manufacturing documentation for GMP compliance. Perform product release activities for finished goods, intermediates, and fills. Provide real-time QA support on the manufacturing floor, including line clearances and in-process checks. Review and approve incoming materials for release into production. Support quality investigations including nonconformances and root cause analysis. Assist with audit readiness, documentation control, and continuous improvement of the Quality Management System. Qualifications Experience in GMP-regulated manufacturing or medical device/pharmaceutical quality environments. Strong understanding of GMP, FDA, and ISO 13485 requirements. Hands‑on experience with batch record review and quality documentation. Strong attention to detail, communication, and organizational skills. Proficiency in Microsoft Office and quality/document control systems preferred. Compensation (MA Pay Transparency) Estimated hourly range: $30–$32/hr (W-2). Final rate within this range will be based on skills, experience, and interview results. #J-18808-Ljbffr JMD Technologies Inc.