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Quality Assurance (Pharmaceutical

Job in City of Syracuse, Syracuse, Onondaga County, New York, 13201, USA
Listing for: The International Society for Pharmaceutical Engineering, Inc.
Full Time position
Listed on 2026-08-13
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager, Production QC/QA, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 55000 - 75000 USD Yearly USD 55000.00 75000.00 YEAR
Job Description & How to Apply Below
Position: Quality Assurance (Pharmaceutical)
Location: City of Syracuse

Quality Assurance Associate (Pharmaceutical)

  • 1-3 years in manufacturing, pharmaceutical, or other regulated environments.
  • Experience with environmental monitoring, quality documentation, or GMP operations.

Are you looking to make a career change to a stable company? This exciting opportunity offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance, vision insurance and paid PTO.Does this position match your future career goals? Then this opportunity could be the right fit for you.

Overview

Responsible for ensuring compliance with GMP standards and quality assurance procedures across production operations. This role supports environmental monitoring, documentation control, and material inspection to maintain high product quality and regulatory compliance.

Key Responsibilities
  • Conduct audits of filling and packaging operations to verify compliance with procedures and standards.
  • Perform environmental monitoring in aseptically classified areas and analyze EM results.
  • Generate, review, and issue production batch records; prepare reports and maintain documentation.
  • Inspect and release materials and components used in production.
  • Monitor equipment charts and documentation to ensure adherence to specifications.
Qualifications
  • 1-3 years in manufacturing, pharmaceutical, or other regulated environments.
  • Experience with environmental monitoring, quality documentation, or GMP operations.
  • Knowledge of GMP and QA procedures.
  • Proficiency with Microsoft Office and related software.
  • Strong analytical, problem-solving, and communication skills.
  • Ability to manage multiple priorities, interpret technical documents, and maintain confidentiality.
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