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 +
- 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