Quality Control Associate
Job description
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