Quality Control Associate

Dawar Consulting; Tucson (AZ); On-site; USD 40,000 - 60,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Paid Sick Leave

401K

Job summary

A consulting firm is seeking a Quality Control Associate in Tucson, AZ. This role involves testing raw materials, maintaining compliance with regulatory standards, and supporting quality assurance processes. Candidates should have a high school diploma and up to 7 years of experience, preferably in a laboratory setting. Strong analytical and documentation skills are essential. Benefits include medical, dental, and 401K. Interested applicants are encouraged to send their resumes.

Qualifications

• 0–7 years of experience in a laboratory or regulated industry.
• Experience in cGMP/GLP/ISO environments preferred.

Responsibilities

• Perform testing of raw materials, in-process materials, and finished goods.
• Maintain accurate documentation and support quality investigations.
• Ensure compliance with regulatory standards.

Skills

Analytical skills

Troubleshooting skills

Data analysis skills

Documentation skills

Organizational skills

Teamwork

Education

High School Diploma

Associate’s or Bachelor’s in Life Sciences

Job description

Quality Control Associate

Tucson, United States | Posted on 04/02/2026

Our client, a global leaderin life sciences and diagnostics, is looking for Quality Control Associate in Tucson, AZ.

Job Duration: Long Term Contract(Possibility Of Extension)

Job Responsibilities

The Quality Control Associate will perform testing of raw materials, in-process materials, and finished goods in a regulated cGMP/ISO 13485 environment. This role is responsible for maintaining accurate documentation, supporting quality investigations, and ensuring compliance with regulatory standards. The ideal candidate will work cross-functionally to support QC operations, reagent manufacturing, and continuous improvement initiatives.

Key Responsibilities

• Perform inspection and testing of raw materials, in-process, and finished goods.
• Document results, complete batch records, and generate QC reports.
• Maintain Device History Records (DHR) and ensure compliance with cGMP and regulatory requirements.
• Conduct data analysis and support process monitoring and trending.
• Investigate Out of Specification (OOS) results and support CAPA activities.
• Perform routine maintenance and calibration checks of lab equipment.
• Support environmental monitoring and maintain QC lab readiness.
• Assist in reagent formulation and manufacturing activities.
• Manage lab inventory, supplies, and vendor coordination.
• Participate in validations, method development, and process transfers.

Quality & Compliance

• Ensure adherence to FDA, ISO, GMP, and OSHA standards.
• Maintain accurate documentation for material handling, storage, and release.
• Support audits, safety reporting, and quality system compliance.

Qualifications

• High School Diploma (Associate’s or Bachelor’s in Life Sciences preferred).
• 0–7 years of experience in a laboratory or regulated industry.
• Experience in cGMP/GLP/ISO environments preferred.

Skills & Requirements

• Strong analytical, troubleshooting, and data analysis skills.
• Excellent documentation and organizational skills.
• Ability to work in a fast-paced, team-oriented environment.
• Familiarity with Lean/6S practices is a plus.

Company Benefits

Medical, Dental, Vision, Paid Sickleave, 401K

If interested, please share your update resume at [e-mail] /[e-mail]