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# Tech Ops and Quality - QA Associate, Quality Operations

- **Company:** TALENTBURST
- **Location:** Norton, MA, United States
- **Experience:** Experienced
- **Contract:** Temporary to permanent
- **Skills:** Document Retrieval, SAP (Applications), Veeva
- **Published:** November 5, 2026
- **Apply:** https://www.thejobnetwork.com/job/50d26ced-51b8-4ba7-8774-96c5aa03b804/tech-ops-and-quality-qa-associate-quality-operations

## About the Role

* Bachelor's degree in a scientific or engineering discipline (Biology, Chemistry, Biotechnology, etc.) or equivalent experience.
 * 2 4 years of GMP experience in Quality, Manufacturing, or QC.
 * Knowledge of cGMP regulations (21 CFR Parts 210/211/11, ICH Q7/Q10) and Good Documentation Practices.
 * Strong attention to detail, organizational skills, and the ability to communicate effectively across teams.
 * Experience with quality systems (e.g., Veeva, SAP) is a plus.

## Description

The QA Associate will help ensure that life-changing biopharmaceutical products are manufactured to the highest standards. The QA Associate will provide day-to-day QA support across manufacturing, validation, materials, QC, engineering and facility operations at our Norton site, partnering with cross-functional teams to maintain GMP compliance and inspection readiness., * Provide raw material support, including review/approval of incoming material documentation and release for GMP use.

 * Deliver on-the-floor QA support to manufacturing, including area clearance and changeover operations, ensuring readiness for production activities.
 * Review and approve SOPs, master batch records (MBRs), specifications, risk assessments, and quality documents.
 * Generate and maintain Quality-related SOPs and controlled forms.
 * Review and approve validation documents and protocol executions to confirm compliance with approved procedures and regulatory requirements.
 * Review and approve QC laboratory qualification documents, including equipment qualification.
 * Perform executed batch record review and approval to ensure accuracy and compliance.
 * Review and approve deviations, CAPAs, Change Controls and related investigations in the quality management system.
 * Support partner audits and regulatory inspections, including document retrieval and subject matter input.
 * Approve work orders in the maintenance system to verify equipment maintenance and calibration compliance.
 * Collaborate with internal cross-functional teams at the Norton facility to drive continuous improvement and quality excellence.