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Qa Operations Associate Jobs (NOW HIRING)

Our QA Operations Specialist manages Quality aspects and projects within area of responsibility as ... associates. * Ensure compliance of site personnel and application of aseptic techniques and full ...

... associates. • Ensure compliance of site personnel and application of aseptic techniques and full ... QA Operations as a valued business partner, with a culture of safety, quality, delivery to patients ...

With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to ... The Manager, QA Operations is responsible for leading QA Operations activities that support ...

Reporting to the Head of Global QA Operations/QP, the Director, QA Operations is responsible for leading Quality Assurance oversight of all Drug Substance (DS) and Drug Product (DP) manufacturing ...

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Qa Operations Associate information

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How much do qa operations associate jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for qa operations associate in the United States is $26.24, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $30.29 per hour, depending on experience, location, and employer.

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For Qa Operations Associate jobs, the most frequently searched job titles are:

QA Operations Associate

Plantation, FL • On-site

Full-time

Posted 15 days ago


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.