Specialist I-QA Product Release

Description
is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider. We currently have an exciting opportunity available for a Quality Assurance Specialist I - Product Release, in Boca Raton, FL !

The Quality Assurance Specialist I- Product Release performs a wide variety of Quality Assurance activities to ensure compliance with related regulatory requirements. This role ensures that all batches meet specifications, are manufactured and packaged in accordance with validated processes and procedures and comply with cGMP and regulatory standards.
Qualifications

• Understand the cGMPs and processes such as Quality Systems (e.g., Deviations, Corrective and Preventive Action reports {CAPAs}, Change Controls, and Out of Specifications {OOSs}).
• Ensure cGMP and regulatory compliance as defined in government regulations such as 21 CFR Parts 11, 210, 211, and 600, as well as compliance with corporate policies and procedures.
• Primary focus is to ensure that all batch releases at are performed in accordance with current approved Standard Operating Procedures (SOPs) and confirm that all supporting documents are received and compliant before release.
• Attend scheduling meetings to coordinate material release priorities as needed
• Communicate any potential delays in the release of batches for manufacturing or commercial distribution
• Assist with investigation reports and Corrective and Preventive Actions (CAPA) in the Quality Management System (QMS) and participate in special projects as required
• Perform review and remediation and support release of manufacturing batch records along with all manufacturing supporting documents including but not limited to logs, charts, specifications, and environmental and WFI data.
• Discuss fundamental technical and regulatory issues, as well as resolve and negotiate quality related issues, as needed.
• Review SOPs and documents in revision from other departments for accuracy and completeness.
• Assist in failure investigations including support in the identification of root causes and corrective actions.

Education Requirements: Bachelor’s Degree but will accept years of experience in lieu of degree.

Experience Requirements: Three to five years in pharmaceutical or biotechnology industry or other related industry.