Quality Inspector

• Job Title:

  Quality Control Technician / Quality Inspector
• Job Description
• The Quality Control Technician is responsible for reviewing, inspecting, dispositioning, approving, and releasing raw materials, labeling, and finished product lots within a cleanroom manufacturing environment.

This role ensures that all materials and products meet established quality standards and documentation requirements, while supporting QA/QC Management with additional quality-related tasks as needed.

• Responsibilities
• + Inspect and disposition incoming raw materials and labels in accordance with established procedures and specifications.

+ Review work order documentation thoroughly prior to product release to ensure completeness, accuracy, and compliance. + Prepare non-conformity documentation for material disposition when quality issues or deviations are identified. + Prepare release documentation and appropriate traceability labeling for incoming materials and finished product lots. + Provide quality control approvals for selected processes performed in the cleanroom manufacturing environment. + Coordinate HPLC testing activities with the Quality Assurance Chemistry team to support product release and investigations. + Conduct proactive reviews of quality-related procedures, including standard operating procedures (SOPs), quality instructions (Q.I.s), RIRs, and component specifications, and highlight opportunities for improvement. + Collaborate with quality leads and management to communicate quality issues, propose solutions, and support corrective and preventive actions. + Use computer systems and Microsoft applications to complete quality records, reports, and documentation accurately and on time. + Perform other quality-related duties as assigned by QA/QC Management to support overall quality system effectiveness.

• Essential Skills
• + High school diploma or equivalent education.

+ Preferably 2 years of inspection experience in a medical device or similar regulated manufacturing environment. + Hands-on experience with inspection of raw materials, labels, and finished products. + Experience working in a cleanroom or controlled manufacturing environment. + Strong attention to detail and focus, with the ability to identify discrepancies and anomalies in materials and documentation. + Basic understanding of good manufacturing practices (GMP) and good documentation practices (GDP). + Ability to read, comprehend, and follow written procedures accurately. + Ability to understand and follow verbal instructions in a fast-paced environment. + Computer proficiency with Microsoft Outlook, Word, and Excel, as well as other software used for quality documentation. + Fluency in English, with the ability to communicate clearly in both written and verbal form. + Ability to communicate ideas, problems, and solutions effectively to quality leads and management. + Ability to collaborate and work productively in a team environment. + Willingness and ability to work overtime and/or weekends based on business needs. + Ability to serve as a backup for second-shift support when required.

• Additional Skills & Qualifications
• + Previous experience in medical device quality control or quality inspection.

+ Familiarity with HPLC testing coordination and interaction with QA Chemistry teams. + Knowledge of reading and interpreting blueprints or technical drawings. + Understanding of quality control principles within a regulated manufacturing setting. + Comfort working with quality procedures such as SOPs, quality instructions, RIRs, and component specifications. + Strong organizational skills to manage multiple lots, documents, and release activities. + Proactive mindset with a willingness to identify and suggest improvements to quality processes.

• Why Work Here?
• Join a growing organization that offers significant opportunities for professional development and career progression. You will contribute directly to the quality and safety of products manufactured in a regulated environment, while working with a supportive team that values collaboration, continuous improvement, and strong quality standards.
• Work Environment
• This role operates in a cleanroom and manufacturing environment that follows strict quality and cleanliness standards.

You will work closely with production, QA/QC, and chemistry teams, using inspection tools, documentation systems, and Microsoft Office applications to complete your tasks. The schedule may include overtime and occasional weekend work depending on business needs, with the possibility of providing backup support for a second shift when required. The environment emphasizes adherence to good manufacturing and documentation practices, teamwork, and consistent, detail-oriented work.

• Job Type & Location
• This is a Contract position based out of Irvine, CA.
• Pay and Benefits
• The pay range for this position is $25.00 - $25.00/hr. Eligibility requirements apply to some benefits and may depend on your jobclassification and length of employment. Benefits are subject to change and may besubject to specific elections, plan, or program terms. If eligible, the benefitsavailable 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)
• Workplace Type
• This is a fully onsite position in Irvine,CA.
• Application Deadline
• This position is anticipated to close on May 27, 2026.
• About Aerotek
• We know that finding work is hard, and finding meaningful work is harder.

Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry - from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies' construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow. Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

• San Francisco Fair Chance Ordinance:

• Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

• Massachusetts Lie Detector:

• It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
• Use of Artificial Intelligence (AI):
• We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates.

AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.