Our client, a world leader in biotechnology and life sciences, is seeking a "Quality Control Associate" based in Tucson, AZ.

Job Duration: Long-Term Contract (Possibility Of Extension)

Rate: $25.75/hr on W2

Company Benefits: Medical, Dental, Vision, Paid Sick Leave, 401K

Summary: The QC Associate supports raw material, in‑process, and finished goods testing in an ISO 13485/cGMP environment. This role performs routine inspections, documents results, maintains lab equipment, and ensures compliance with quality and safety standards. The individual will work with complex systems, support investigations (OOS/non‑conformance), maintain inspection‑ready labs, and generate QC documentation for Device History Records.

Key Responsibilities:

Perform testing of raw materials, in‑process samples, and finished goods
Document results, complete batch records, and generate qualification reports
Conduct data analysis and support OOS/non‑conformance investigations
Maintain QC lab, equipment, and records per cGMP and OP requirements

Requirements:

HS Diploma + 7 years experience, OR Associate’s + 3 years, OR Bachelor’s + <1 year
Hands‑on lab experience; strong data analysis and troubleshooting skills
Accurate pipetting, attention to detail, and ability to meet deadlines
Experience in regulated environments (GLP, cGMP, ISO) preferred
Ability to lift 25 lbs and work on feet for extended periods

If interested, please share your updated resume at hr@dawarconsulting.com/lakshmi@dawarconsulting.com

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