Quality Control Associate
Dawar Consulting
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:
Quality control, GMP, Laboratory Skills
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
- 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
Quality control, GMP, Laboratory Skills
Vacancy posted 3 days ago
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