Confirmed on the employer's own hiring board on Oct 13, 2026. First seen by Alion on Oct 12, 2026.
Our client, a world leader in biotechnology and life sciences, is seeking a "Quality Control Associate " based inTucson, 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/>
- 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 [email protected] / [email protected]

