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Senior Quality Assurance Associate

Job in Hightstown, Mercer County, New Jersey, 08520, USA
Listing for: Eugia US LLC
Full Time position
Listed on 2026-08-24
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers
Salary/Wage Range or Industry Benchmark: 27 - 29 USD Hourly USD 27.00 29.00 HOUR
Job Description & How to Apply Below
Location: Hightstown

Senior Quality Assurance Associate

As a Senior Quality Assurance Associate, you will provide strategic quality support to warehouse and distribution operations. This role ensures compliant receipt, inspection, and release of pharmaceuticals through adherence to GDP, DSCSA serialization requirements, and FDA import regulations. You will independently manage deviations and nonconformances, lead supplier quality assessments, drive CAPA closure and verification, maintain regulatory compliance documentation, and support Quality leadership on cross-functional initiatives and regulatory interactions.

Responsibilities

  • Lead receipt and inspection of pharmaceutical products for compliance with GDP, DSCSA, and regulatory requirements.
  • Verify DSCSA serialization, lot traceability, and chain of custody documentation.
  • Identify and manage suspect or illegitimate product reports.
  • Monitor warehouse environmental conditions and storage compliance.
  • Inspect returned goods for disposition and regulatory compliance.
  • Write, revise, and approve QA documentation (SOPs, procedures, work instructions).
  • Investigate and resolve deviations and nonconformances.
  • Execute QA review and approval of product release documentation.
  • Support continuous improvement activities to enhance Quality operations and regulatory compliance.

Qualifications - Skills & Requirements

  • Good knowledge of Microsoft Office applications.
  • Organizational and leadership skills.
  • Excellent data collection and analysis skills.
  • Keen attention to detail, and critical/logical thinking
  • Strong knowledge of GMP regulations and their application.
  • Demonstrated ability to communicate technical information or complex situations to supervisor or area management in a concise and clear manner.
  • Excellent verbal, written, and teamwork communication skills.

Education & Experience

  • Minimum B.S. degree; preferably in a scientific field.
  • 2-3 years of experience in Quality Assurance or a similar field within the pharmaceutical industry.
  • Oracle experience (preferred).

Compensation

MinUSD $27.00/Hr. MaxUSD $29.00/Hr.

Physical Requirements

WAREHOUSE OR PRODUCTION POSITION – While performing the duties of this job the employee is required to:
Regularly lift and/or move objects 10-50lbs Frequently required to stand, walk, stoop, kneel, crouch or crawl Occasionally required to sit and climb or balance Specific vision abilities required for this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust and focus The worker is subject to environmental conditions. Protection from weather conditions but not necessarily from temperature changes The worker is subject to both environmental conditions.

Activities occur inside and outside Medium work Exerting up to 50 pounds of force occasionally, and/or up to 30 pounds of force frequently, and/or up to 10 pounds of force constantly to move objects. Additional Physical Requirements Blood/Fluid Exposure Risk Category III:
Tasks involve no exposure to blood, body fluids or tissues. Category I tasks are not a condition of employment.

Position Requirements
10+ Years work experience
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