Quality Assurance Associate III

Job Title

Quality Assurance Associate III

The QA Associate III is responsible for monitoring laboratory and manufacturing process verifications to ensure compliance with operating procedures and specifications. This role involves performing process monitoring, labeling control, reinspection process monitoring, and sampling processes for Reserved Samples. Additionally, the QA Associate III provides quality oversight on manufacturing processes to ensure compliance, including data integrity, and supports quality investigations and resolutions of quality issues.

• Monitor laboratory and manufacturing processes to ensure compliance with procedures and specifications.
• Perform process monitoring, labeling control, and reinspection process monitoring.
• Conduct sampling processes for Reserved Samples.
• Provide quality oversight on laboratory and manufacturing processes to ensure compliance, including data integrity.
• Support quality investigations and resolve quality issues.

• Minimum of Bachelor’s degree in Science with 3+ years of experience in quality assurance or QC within the medical device or pharma industry, or a high school diploma with 4-5 years of relevant experience.

• Excellent communication and critical thinking skills.
• Ability to work a non-standard schedule as needed.
• Regular and predictable on-site attendance.

This is an onsite role with working hours from Sunday to Thursday, 8am to 5pm. The work environment is dynamic and fast‑paced, reflecting the high standards and demands of the medical device industry.

This is a Contract position based out of Irvine, CA.

The pay range for this position is $32.00 – $33.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre‑tax and Roth post‑tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long‑term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Irvine, CA.

This position is anticipated to close on Jan 24, 2026.

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccom