What are the responsibilities and job description for the QA Compliance Specialist position at JMD Technologies Inc.?
Title: QA Compliance Specialist
Location: Bedford, MA (On-site)
Employment Type: Contract (6 months expected)
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
• Bachelor’s degree or equivalent experience.
• 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.
Salary : $30 - $32