QA Operations Associate Goodwin Biotechnology Inc - 2.8 Plantation, FL Job Details Full-time 2 hours ago Qualifications Data integrity assurance Investigations regulatory compliance Internal investigations High school diploma or GED Manufacturing facility experience Investigating compliance violations Aseptic technique Pharmaceutical manufacturing facility experience

Full Job Description Description:

Scope of Function:

The QA Operations Associate is a hands-on, on-the-floor Quality Assurance professional responsible for ensuring GMP compliance during manufacturing operations while exercising independent quality judgment. The role provides real-time QA oversight and acts as a QA representative on the manufacturing floor, with responsibility for assisting in investigations, and escalation of quality risks.

Specific Duties:

Provide real-time QA presence and oversight for manufacturing operations in classified areas. Perform routine and ad hoc GMP walkthroughs to assess compliance and aseptic practices. Act as the primary QA point-of-contact during manufacturing activities. Exercise independent GMP decision-making, including escalation and stopping operations when required. support deviation investigations. Real-time review and approval of executed batch records, logbooks, and cleaning documentation. Support media fills, line clearances, and room/equipment release. Review, SOPs, batch records, and specifications. Support audits, inspections, and inspection readiness. Coordinates the archiving of executed manufacturing records with QA Documentation Control. Supports preparation of batch Certificate of Compliance and Certificate of Assurance, as applicable. Provide QA support for the electronic environmental system and the NetSuite enterprise system. This job description summarizes the primary responsibilities of the role and does not represent a complete list of all duties. Duties and responsibilities may be modified, expanded, or reassigned at any time based on business needs.

Requirements:

Education & Qualifications:

High school diploma minimum; Associate or Bachelor's degree preferred. Strong knowledge of cGMP, aseptic manufacturing, and data integrity. 1 year+ GMP experience; independent floor oversight; support investigations.