Quality Control Associate
Job in
Tucson, Pima County, Arizona, 85718, USA
Listed on 2026-05-29
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
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.
- 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.
- 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.
- 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.
Medical, Dental, Vision, Paid Sickleave, 401K
If interested, please share your update resume at /
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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