Quality Inspector @ Aerotek

Job Title: Quality Inspector / Quality Control TechnicianJob DescriptionThe Quality Control Technician plays a key role in ensuring that raw materials, labels, and finished products meet all quality standards before release. This position reviews documentation, inspects and dispositions materials, prepares and maintains quality records, and provides quality approvals for processes in a cleanroom manufacturing environment. The role also supports quality assurance and chemistry teams and contributes to continuous improvement of quality procedures.

Responsibilities

• Inspect and disposition incoming raw materials and labels in accordance with established quality standards and procedures.
• Review work order documentation thoroughly prior to product release to ensure accuracy, completeness, and compliance.
• Prepare non-conformity documentation for material disposition when quality issues or deviations are identified.
• Prepare release documentation and apply appropriate traceability labeling for incoming materials and finished product lots.
• Provide quality control approvals for selected manufacturing processes within the cleanroom environment.
• Coordinate HPLC testing activities with the quality assurance chemistry team to support material and product verification.
• Proactively review quality-related procedures, including standard operating procedures (SOPs), quality instructions (Q.I.s), report of irregularities (RIRs), and component specifications, and provide feedback for improvements.
• Communicate ideas, problems, and proposed solutions clearly to quality leads and management to support effective decision-making.
• Collaborate with team members to maintain a consistent and compliant quality control process across all operations.
• Complete other quality-related duties and special assignments as directed by QA/QC management.

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 and quality control of raw materials, labels, and finished products.
• Ability to work in a cleanroom manufacturing environment following strict cleanliness and procedural standards.
• Strong attention to detail and focus, with the ability to identify discrepancies, anomalies, and non-conformities.
• Basic understanding of good manufacturing practices (GMP) and good documentation practices (GDP).
• Ability to read, comprehend, and follow written procedures and quality documentation.
• Ability to understand and follow verbal instructions in a fast-paced production environment.
• Proficiency with Microsoft Outlook, Word, and Excel, and the ability to learn other computer software packages as needed.
• Fluency in English with the ability to communicate clearly in both written and verbal forms.
• Ability to communicate ideas, problems, and solutions effectively to quality leads and management.
• Ability to collaborate and work effectively in a team-oriented environment.
• Willingness and ability to work overtime and/or weekends according to business needs.
• Ability to serve as back-up support for second shift when required.

Additional Skills & Qualifications

• Experience in medical device inspection and quality control is strongly preferred.
• Familiarity with cleanroom protocols and cleanroom manufacturing processes.
• Exposure to HPLC testing coordination or working with a chemistry or laboratory team.
• Ability to interpret basic blueprints or product specifications used in manufacturing and inspection.
• Comfort with working under established SOPs, quality instructions, and component specifications.
• Demonstrated reliability and accountability in maintaining accurate quality records and documentation.
• Strong problem-solving mindset with a proactive approach to identifying and addressing quality issues.

Why Work Here? You will join a growing organization that offers significant opportunity for development and advancement as the business expands. The environment values quality, teamwork, and continuous improvement, providing the chance to build your skills in a regulated manufacturing setting. You can expect a culture that encourages collaboration, supports learning, and recognizes the contributions of employees who help maintain high standards and drive the companys success.

Work EnvironmentThis role is based in a cleanroom manufacturing environment where strict cleanliness, safety, and procedural standards are followed. You will work closely with production and quality assurance teams on the manufacturing floor, handling raw materials, labels, and finished products. The position may require overtime and weekend work depending on business needs, and occasional support of a second shift. The environment is structured and process-driven, with regular use of computers and Microsoft Office applications for documentation and communication.

Job Type & LocationThis is a Contract to Hire position based out of Irvine, CA.

Pay and BenefitsThe pay range for this position is $25.50 - $25.50/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. 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)

Application DeadlineThis position is anticipated to close on Nov 12, 2026.

Workplace TypeThis is a fully onsite position in Irvine,CA.

About Aerotek

Aerotek® Inc. provides staffing and services solutions in manufacturing, logistics, construction, aviation, facilities and maintenance. We provide the expertise, solutions and people required to rise to the challenges of North American industry. Headquartered in Hanover, Md., Aerotek operates a unified network of over 200 offices across North America, supporting more than 18,000 clients each year. Aerotek is an Allegis Group company, the global leader in workforce and business solutions. To learn more, visit: Aerotek.com | 1-888-AEROTEK.

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.