QA Technician

Job Title:

QA Technician Job Description The QA Technician supports manufacturing operations by ensuring products and processes comply with applicable standards, regulations, and internal quality procedures. This role performs in-process and final inspections, manages quality documentation, and collaborates closely with manufacturing teams to enable the timely release of compliant products. The QA Technician follows detailed SOPs, contributes to a strong quality culture, and provides training on quality-related tasks to other employees. Responsibilities Review incoming orders to assess compliance with applicable standards and regulatory requirements. Perform in-process testing of devices, including post-manufacturing and post-sterilization inspections, to verify product quality. Conduct final product inspections and accurately document product release activities. Summarize inspection and test data, and coordinate with manufacturing supervisors to support efficient and timely product release. Follow detailed procedures documented in SOPs, work instructions, forms, and checklists to ensure consistent execution of quality tasks. Manage forms and manufacturing facility procedures in compliance with organizational guidelines and quality system requirements. Ensure manufacturing facility procedures comply with SOPs, applicable GMP and cGMP requirements, and relevant standards. Maintain and organize customer-related files and documentation so they are complete, current, and easily retrievable. Ensure consistency and compliance of document structure with established SOPs, standards, and applicable cGMP regulations. Adhere to the company's purpose and operating principles to help build a positive and productive team culture. Comply with all company policies, procedures, and safety protocols, including appropriate use of PPE when required. Access employee and/or patient PHI and ePHI only as needed for job-related functions, maintaining confidentiality and data integrity. Train employees on the job duties associated with the Quality Assurance Technician I role, sharing best practices and quality expectations. Accurately collect, organize, and record quality and inspection data for analysis and reporting. Read, interpret, and apply Standard Operating Procedures and work instructions in daily activities. Use measurement equipment such as calipers, micrometers, scales, and comparators to perform precise inspections. Apply basic mathematical functions, including whole numbers, fractions, decimals, averages, rates, and percentages, and interpret bar graphs as part of data analysis. Collaborate and communicate effectively with cross-functional teams to resolve quality issues and support continuous improvement. Prioritize multiple tasks, manage time effectively, and work within deadlines in a fast-paced manufacturing environment. Perform other duties as assigned to support quality assurance and manufacturing operations. Essential Skills Prior quality assurance experience in a manufacturing or similar regulated environment. Associate's degree in a technical or business-related field; a Bachelor's degree is preferred. Ability to use measurement equipment such as calipers, micrometers, scales, and comparators. Working knowledge of 21 CFR Part 820 regulations preferred. Working knowledge of

ISO 13485

2016 or similar standards and experience with Quality Management Systems preferred. Understanding of GMP and cGMP principles and FDA regulatory expectations related to manufacturing quality and regulatory compliance. Strong documentation skills with the ability to accurately complete and maintain quality records and forms. Strong organizational skills with the ability to manage multiple documents, procedures, and tasks simultaneously. Ability to read, write, and follow verbal and written instructions clearly and accurately. Ability to read and interpret SOPs and work instructions and apply them consistently in daily work. Ability to accurately collect, organize, and interpret data for quality and process evaluations. Proficiency in basic mathematics, including whole numbers, fractions, decimals, averages, rates, and percentages, and the ability to draw and interpret bar graphs. Excellent written and verbal communication skills for effective interaction with cross-functional teams. Proficiency with Microsoft Office programs, including Word, Excel, and PowerPoint. Ability to work both independently and as part of a dynamic team, demonstrating strong collaboration skills. Detail-oriented mindset with a focus on accuracy and compliance in all quality-related activities. Ability to multi-task and work within deadlines in a production environment. Willingness to work a flexible schedule, including some evenings and weekends depending on workload. Strong analytical and problem-solving skills. Ability to establish and maintain effective working relationships with cross-functional teams. Additional Skills & Qualifications Bachelor's degree in a technical or business-related field is preferred. At least 1 year of experience in a radiation-controlled environment is preferred. Prior experience with Quality Management Systems and regulatory compliance in a manufacturing setting is preferred. Prior experience in clean room operations and environmental monitoring testing is preferred. Familiarity with quality inspection tools and techniques used in regulated manufacturing environments. Experience working under FDA regulations and within a structured Quality Management System. Demonstrated ability to train others on quality procedures and job-specific tasks. Experience working with hazardous materials and chemicals while following appropriate safety protocols. Comfort working in environments that include office space, supply rooms, laboratories, and clean rooms. Why Work Here? This opportunity offers a clear path from contract to hire, giving you the chance to demonstrate your skills and grow into a long-term, full-time role. You receive interview preparation and support throughout the process, helping you present your experience confidently. The organization values internal growth, providing opportunities to develop your expertise, take on additional responsibilities, and advance your career over time. You join a team-focused culture that emphasizes collaboration, continuous learning, and a strong commitment to quality and compliance. Work Environment The role operates across office space, supply rooms, laboratories, and clean room environments within a regulated manufacturing setting. You frequently work with laboratory and manufacturing equipment, as well as hazardous materials and chemicals, and you use appropriate personal protective equipment and safety precautions at all times. The position requires frequent fine hand-eye coordination, regular use of a computer, keyboard, mouse, monitor, and other office equipment, and routine handling of measurement devices such as calipers, micrometers, scales, and comparators. The work is largely stationary, with some movement between work areas, and includes regularly lifting, carrying, and moving items weighing up to 50 pounds. The schedule may occasionally include evening and weekend work depending on workload, and some overnight travel may be required for work-related activities and events. The environment emphasizes strict adherence to SOPs, GMP and cGMP requirements, and quality and safety protocols throughout daily operations. Job Type & Location This is a Contract to Hire position based out of Richland, WA. Pay and Benefits The pay range for this position is $21.00 - $23.00/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) Workplace Type This is a fully onsite position in Richland,WA.

Application Deadline This position is anticipated to close on May 8, 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.