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Quality Control Associate

Job in Tucson, Pima County, Arizona, 85718, USA
Listing for: Dawar Consulting
Full Time position
Listed on 2026-05-29
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager, Data Analyst
Salary/Wage Range or Industry Benchmark: 40000 - 60000 USD Yearly USD 40000.00 60000.00 YEAR
Job Description & How to Apply Below

Quality Control Associate

Tucson, United States | Posted on 04/02/2026

Our client, a global leaderin life sciences and diagnostics, is looking for Quality Control Associate in Tucson, AZ.

Job Duration:
Long Term Contract(Possibility Of Extension)

Job Responsibilities

The Quality Control Associate will perform testing of raw materials, in-process materials, and finished goods in a regulated cGMP/ISO 13485 environment. This role is responsible for maintaining accurate documentation, supporting quality investigations, and ensuring compliance with regulatory standards. The ideal candidate will work cross-functionally to support QC operations, reagent manufacturing, and continuous improvement initiatives.

Key Responsibilities
  • Perform inspection and testing of raw materials, in-process, and finished goods.
  • Document results, complete batch records, and generate QC reports.
  • Maintain Device History Records (DHR) and ensure compliance with cGMP and regulatory requirements.
  • Conduct data analysis and support process monitoring and trending.
  • Investigate Out of Specification (OOS) results and support CAPA activities.
  • Perform routine maintenance and calibration checks of lab equipment.
  • Support environmental monitoring and maintain QC lab readiness.
  • Assist in reagent formulation and manufacturing activities.
  • Manage lab inventory, supplies, and vendor coordination.
  • Participate in validations, method development, and process transfers.
Quality & Compliance
  • Ensure adherence to FDA, ISO, GMP, and OSHA standards.
  • Maintain accurate documentation for material handling, storage, and release.
  • Support audits, safety reporting, and quality system compliance.
Qualifications
  • High School Diploma (Associate’s or Bachelor’s in Life Sciences preferred).
  • 0–7 years of experience in a laboratory or regulated industry.
  • Experience in cGMP/GLP/ISO environments preferred.
Skills & Requirements
  • Strong analytical, troubleshooting, and data analysis skills.
  • Excellent documentation and organizational skills.
  • Ability to work in a fast-paced, team-oriented environment.
  • Familiarity with Lean/6S practices is a plus.
Company Benefits

Medical, Dental, Vision, Paid Sickleave, 401K

If interested, please share your update resume at  /

#J-18808-Ljbffr
Position Requirements
10+ Years work experience
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