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 View email address on click.appcast.io/View email address on click.appcast.io

Skill Set
Quality control, GMP, Laboratory Skills