QA Associate, Quality Operations

Integrated Resources, Inc
  • Norton, MA
  • $40–$46 Per Hour
  • Quick Apply
14 days ago

Job Description

Title: QA Associate, Quality Operations
Location: Norton, MA
Duration: 6months+
Pay: $40-46/hr. on w2

About the Role:
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.

Key Responsibilities:
  • 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.
Qualification/Skills:
  • 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.

Numbers & Facts

LocationNorton, MA
Salary$40–$46 Per Hour

Skills

  • Biologyunmatched
  • Biotech and Pharmaceuticalunmatched
  • Calibrationunmatched
  • Change Controlunmatched
  • Chemistryunmatched
  • Communication Skillsunmatched
  • Continuous Improvementunmatched
  • Cross-Functionalunmatched
  • Detail Orientedunmatched
  • Documentationunmatched
  • Equipment Maintenance/Repairunmatched
  • GMP (Good Manufacturing Practices)unmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Organizational Skillsunmatched
  • Process Improvementunmatched
  • Quality Assuranceunmatched
  • Quality Controlunmatched
  • Quality Managementunmatched
  • Regulationsunmatched
  • Regulatory Requirementsunmatched
  • Risk Analysisunmatched
  • SAPunmatched
  • Standard Operating Procedures (SOP)unmatched
  • Validation Documentationunmatched
  • Validation Planunmatched

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