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Salary
$50k per year
Location
In office (Tucson)
Seniority
Middle · 3+ years exp
Employment
Contractor

Confirmed on the employer's own hiring board on Oct 13, 2026. First seen by Alion on Oct 12, 2026.

Overview
Company
Impact
Profile match
Dawar Consulting is a staffing and professional services firm headquartered in Newark, California, in Silicon Valley, that provides contract, direct-hire and managed-services staffing alongside Workday HCM and ServiceNow implementation and support. Besides its California head office it has offices in Noida in India, Utrecht in the Netherlands and Mexico City, and its life science practice places scientists and lab staff with biotechnology and pharmaceutical clients on long-term contracts. Its openings are mostly client placements such as research associates, scientists, QC chemists, lab technicians and bioprocess engineers, plus SAP consultants and technical recruiters.

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]

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