Quality assurance technician jobs in Tacoma, WA - 367 jobs

At Food Lion, Associates are the most important assets to our organization. We want associates to have meaningful careers full of variety and challenges. Each associate contributes to the overall success of Food Lion, and in return, we strive to provide all associates with a fulfilling work experience and reward performance and commitment. We are committed to the professional development of our associates through on-the-job learning opportunities and training. At Food Lion, Associates are the most important assets to our organization. We want associates to have meaningful careers full of variety and challenges. Each associate contributes to the overall success of Food Lion, and in return, we strive to provide all associates with a fulfilling work experience and reward performance and commitment. We are committed to the professional development of our associates through on-the-job learning opportunities and training. Food Lion provides equal employment opportunities to all associates and applicants for employment without regard to race, color, religion, sex (including pregnancy, childbirth and related conditions) national origin, age, disability, sexual orientation, veteran status, gender identity or gender expression or any other characteristic protected by law. If you have a disability and require assistance in the application process, please contact our Recruiting Department at ***********************

We are seeking a highly organized and hands-on Robotics Lab Technician (Contract) to support daily operations in our robotics research lab. This role ensures efficient, safe, and reliable experiments across multiple robotics platforms and research projects. The ideal candidate will manage lab operations, equipment, and workflows. They will coordinate lab usage and improve the lab environment to support fast-paced research and development. Key Responsibilities * Set up, maintain, and continuously improve the robotics lab space to support ongoing research and experimentation * Ensure the lab remains safe, clean, well-organized, and clutter-free at all times * Coordinate lab scheduling and access to enable multiple experiments to run efficiently without conflict * Enforce lab safety policies and ensure all personnel complete required safety and equipment training * Act as the main contact for inquiries about lab usage, tools, robots, and infrastructure * Manage shared tools, equipment, and consumables, including inventory tracking and replenishment * Operate and manage 3D printing and laser cutting workflows, including job scheduling, material handling, and basic equipment maintenance * Coordinate robot maintenance and repairs by diagnosing issues, performing basic fixes, and working with engineers or external vendors as needed * Proactively identify and implement improvements to lab layout, workflows, documentation, and operational efficiency * Support the setup and execution of demos, experiments, and lab tours for visitors, collaborators, and leadership Required Qualifications * Experience working in an industrial, scientific, or engineering lab environment; robotics lab experience strongly preferred (or equivalent experience) * Hands-on experience with lab equipment, tools, and standard safety procedures * Familiarity with robotics systems, electromechanical hardware, or other complex technical equipment * Experience managing shared resources and coordinating usage across multiple users or teams * Strong organizational skills with a demonstrated ability to maintain orderly, efficient technical spaces * Experience operating or managing fabrication tools such as 3D printers and laser cutters * Working knowledge of lab safety standards and guidelines * Ability to troubleshoot hardware issues and coordinate repairs effectively * Strong communication skills and confidence in serving as the main "go-to" person for lab-related questions *Job Type & Location*This is a Contract position based out of Seattle, WA. *Pay and Benefits*The pay range for this position is $30.00 - $50.00/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 Seattle,WA. *Application Deadline*This position is anticipated to close on Jan 23, 2026. h4>About TEKsystems: We're partners in transformation. We help clients activate ideas and solutions to take advantage of a new world of opportunity. We are a team of 80,000 strong, working with over 6,000 clients, including 80% of the Fortune 500, across North America, Europe and Asia. As an industry leader in Full-Stack Technology Services, Talent Services, and real-world application, we work with progressive leaders to drive change. That's the power of true partnership. TEKsystems is an Allegis Group company. 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. About TEKsystems and TEKsystems Global Services We're a leading provider of business and technology services. We accelerate business transformation for our customers. Our expertise in strategy, design, execution and operations unlocks business value through a range of solutions. We're a team of 80,000 strong, working with over 6,000 customers, including 80% of the Fortune 500 across North America, Europe and Asia, who partner with us for our scale, full-stack capabilities and speed. We're strategic thinkers, hands-on collaborators, helping customers capitalize on change and master the momentum of technology. We're building tomorrow by delivering business outcomes and making positive impacts in our global communities. TEKsystems and TEKsystems Global Services are Allegis Group companies. Learn more at TEKsystems.com. 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.

Seattle, WA PAY RATE $22/hr REPORTS TO: The Laboratory Technician reports directly to the Laboratory Manager, with dotted-line reporting to the Quality Assurance Manager (QAM). A Laboratory Technician (Tech) is a bench chemistry associate whose main responsibility is to perform routine operations within a laboratory setting. This includes preparing reagents, cleaning glassware, organizing and sorting supplies, and logging in samples. The Tech may also be specialized in one type of analysis for the purposes of improving laboratory workflow. The Tech is responsible for following all documented procedures, recording all laboratory notes, and elevating technical issues to the laboratory manager. RESPONSIBILITIES AND DUTIES: o Ensure that all samples received by the laboratory are logged in according to the appropriate procedure including labeling, logging, and acknowledging o Maintain a clean and organized lab space o Prepare reagents at the direction of the Laboratory Manager o Perform a specific analysis, or portion of analysis, at the direction of the Laboratory Manager o Report non-conformances to the QAM and Laboratory Manager QUALIFICATIONS: o HS Diploma or GED equivalent. Associates Degree or higher in a physical science preferred. o General familiarity with laboratory safety. Previous laboratory experience preferred. o Ability to follow written or verbal instructions o Intermediate skill level (or above) in Microsoft Word, Excel, and Outlook. o Professional appearance and behavior o Ability to pass a background check and drug screen o Valid driver's license o Approved to be employed in the United States PHYSICAL REQUIREMENTS: o Must be able to meet the physical demands of a typical laboratory environment o Sitting/standing, reaching overhead cabinets o Possible light lifting KEY BENEFITS INCLUDE: Medical, Dental, and Vision Insurance Flexible Spending Accounts 401(K) Plan with Competitive Match Continuing Education and Tuition Assistance Employer-Sponsored Disability Benefits Life Insurance Employee Assistance Program (EAP) Paid Time Off (PTO), Paid Holidays, & Bonus Floating Holiday (if hired before July 1st) Profit Sharing or Individual Bonus Programs Referral Program Per Diem & Paid Travel Employee Discount Hub EEO Commitment: We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, national origin, ethnicity, sex, pregnancy, sexual orientation, gender identity/expression, including transgender identity, religion, disability, age, genetics, active military or veteran status and any other characteristics protected under applicable federal or state law. #LABS Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

Join our Team: Quality Assurance Technician 40 Hours/Monday-Thursday Join our team at Terex/Genie and embark on an exciting opportunity as we seek a skilled and dedicated Quality Assurance Technician to contribute to the Operations team. At Terex / Genie we believe in fostering a vibrant and inclusive work culture where every person is empowered to thrive. We're dedicated to driving quality, innovation, embracing diversity, and creating an environment where everyone feels valued and respected. We're committed to excellence in everything we do, and we're seeking talented individuals who share our passion and values to join our team. This is a technical position requiring in-depth knowledge of production processes and Genie products. To advance to this position prospective incumbents will demonstrate the ability to record, analyze, and resolve measured and observed quality problems according to specifications and standards. Advancement potential exists from this position to areas such as small group leadership or to Engineering Technician. Duties and Responsibilities Interprets engineering drawings, schematic diagrams, and formulas to determine quality and reliability standards. Selects parts, components and products for inspection and testing. Inspects and tests components, parts, and assembled products for workmanship, compliance with specifications and regulatory standards. Employs techniques such as electronic and conventional measurement, observation, functional tests, and destructive tests. Conducts non-destructive tests of welding and fastened joints. Evaluates data and writes modifications of existing quality or production standards to maximize quality within limits of machine capability and cost. Confers with Design Engineers and Manufacturing to identify, diagnose, and resolve non-conforming quality problems including those associated with parts, components, or the manufacturing process. Contacts parts suppliers (internal and external) to resolve quality matters. Corrects sub-standard work or replaces parts using hand and power tools. May specialize in incoming materials, design, process control, research and development, product overall reliability, warranty, or other phase of production where quality reviews are involved. Works with customers to resolve warranty issues. Performs other duties as assigned that support the overall objective of the position. Qualifications Knowledge and Skills The required knowledge may vary based on the specific requirements of different operating units. In general, the position requires an in-depth knowledge of Genie products and components including electronics, electrical circuits, mechanics, pneumatics, hydraulics, power transmission, and structural members. Requires an in depth understanding of Genie production processes. Requires sufficient math skills to read and record detailed measurements. Requires well-developed problem-solving skills to identify and remedy problems non-conforming quality related to materials, parts, or production. Requires working knowledge of inspecting and testing procedures. Requires sufficient human relations skills to discuss quality issues and resolve conflict. Abilities Requires the ability to carry out all aspects of the position. Requires the ability to translate engineering instructions and blueprints into assembly and parts quality and reliability standards. Requires the ability to inspect and test electrical-mechanical parts and equipment. Requires the ability to enter quality and reliability data onto a personal computer using a keyboard. Requires the ability to learn and convey the principles of lean manufacturing. Physical Abilities Requires ambulatory ability to walk, stand, bend, and stoop for extended periods of time. Requires sufficient hand-arm-eye coordination to guide and place objects. Requires the ability to lift, pull or push into place light to medium weight (10-50 pounds) objects on an frequent basis. Requires visual acuity to observe precision numbers, notice mechanical and electrical problems, and read numbers and letters. Requires auditory ability to project voice and hear in a production environment. Education and Experience The position requires a high school diploma. Preferred qualifications also include two years of college-level coursework in manufacturing or engineering technology, and two years of experience in automotive or equivalent assembly and production line setup. Additional experience in quality assurance or process control can substitute for higher education. The salary range for this role is $31-$40 hourly with opportunity for overtime. Why Join Us • We are a global company, and our culture is defined by our Values - Integrity, Respect, Improvement, Servant Leadership, Courage, and Citizenship. Check out this video! The Terex purpose • Safety is an absolute way of life. We expect all team members to prioritize safety and commit to Zero Harm. • Our top priority is creating an inclusive environment where every team member feels safe, supported, and valued. • We make a positive impact by providing innovative solutions, engaging our people, and operating in a sustainable way. • We are committed to helping team members reach their full potential. • Through innovation and collaboration, our vision remains forward-looking, and we aim to be a catalyst for change, inspiring others to build a better world for generations. • We offer competitive salaries, Team Member bonus of 3%, hybrid working, private healthcare, 8 holidays, pension, life assurance, LinkedIn Learning, on site free parking. • For more information on why Terex is a great place to work click on the link! Careers | Terex Corporate This above description is non-exhaustive and there may be additional duties in accordance with the role. If you are interested in an open position but feel you may not meet all the listed qualifications, we still encourage you to apply. How to Apply To apply for this role and view all available positions within Terex, please visit our careers page: ********************* Terex is an equal opportunity employer and appointments are based on merit. We value diversity and welcome applications from all sections of our community. If you are interested in an open position but feel you may not meet all the listed qualifications, we still encourage you to apply. About Terex: Terex Corporation is a global industrial equipment manufacturer of materials processing machinery, waste and recycling solutions, mobile elevating work platforms (MEWPs), and equipment for the electric utility industry. We design, build, and support products used in maintenance, manufacturing, energy, minerals and materials management, construction, waste and recycling, and the entertainment industry. We provide best-in-class lifecycle support to our customers through our global parts and services organization, and offer complementary digital solutions, designed to help our customers maximize their return on their investment. Certain Terex products and solutions enable customers to reduce their impact on the environment including electric and hybrid offerings that deliver quiet and emission-free performance, products that support renewable energy, and products that aid in the recovery of useful materials from various types of waste. Our products are manufactured in North America, Europe, and Asia Pacific and sold worldwide. Additional Information: We are passionate about producing equipment that helps improve the lives of people around the world and providing our team members with a rewarding career and the opportunity to make an impact. We are committed to recruiting, engaging, developing, and retaining team members at all levels of our global workforce. Our culture is defined by our Terex Way Values - Integrity, Respect, Improvement, Servant Leadership, Courage, and Citizenship. Our values are the driving force behind our commitment to maintain an inclusive, supportive, non-discriminatory, and safe workplace for all team members. To that end, we are committed to actively foster a culture where every team member feels valued, listened to, and appreciated. We are committed to being fair and impartial in our decisions. As an Equal Opportunity Employer, employment decisions are made without regard to race, color, religion, national origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. If you are a qualified individual with a disability, including disabled veterans, you may request a reasonable accommodation if you are unable or limited in your ability to access job openings or apply for a job on this site as a result of your disability. You can request reasonable accommodations by contacting the recruiting department (person or department) at ********************************** . The Company offers competitive salaries, advancement opportunities, and a full range of benefits, including paid vacation, 401(k), medical, dental, and vision.

Job DescriptionQuality Technician IIRapidly Growing Renewable Energy Company Seattle Area/Relocation Assistance Available$26 per hour, with potential flexibility based on experience Terrific Quality Technician position with a rapidly growing renewable energy company. The position will ensure quality and compliance for products and services manufactured. Previous quality control experience in a fast paced production environment is essential for this role.Responsibilities: Ensure production lines adhere to and comply with legal requirements, standards, and procedures Provide training to productions teams to improve quality control and product excellence Review and interpret blueprints, drawings, and radiographs Perform testing on the production line and propose improvements Collect quality data and provide statistical analysis reports Monitor operations and suggest improvements to processes Qualifications: Prior experience in a fast paced production environment Manufacturing experience within a technical role, experience with PV module is preferred Strong problem solving skills Tech savvy Ability to work collaboratively in a team environment and also independently Equal opportunity employer

Job Description The Analyst II or III or IV Quality Control Technician is primarily responsible for preparing and maintaining quality control materials and all related record documentation used at Navis Clinical Laboratories to monitor analytical test accuracy. The Quality Control Tech reports to Analytical Manager. The Quality Control Technician will assist the Laboratory Director and Quality Manager in the maintenance of quality control records which may be reviewed during various compliance audits and inspections including but not limited to CLIA, the College of American Pathologists, the Washington Department of Health or any other agency that may have regulatory oversight. The schedule for this 6am - 2:30pm Monday- Friday or Tuesday-Saturday. Essential Functions: Prepare various quality control materials used to monitor analytical test accuracy including those for initial immunoassay testing, confirmatory testing, specimen validity testing and other testing as dictated by client demand and growth. These include but are not limited to: Open quality control material Blind quality control material Internal standards Prepare various chemicals and reagents used in the performance of tests performed by the laboratory Develop and maintain systems for the documentation of all quality control materials Assist in the collation and reporting of proficiency testing results Assist in the preparation of records and materials required for compliance audits Monitor, perform maintenance, and document maintenance of lab equipment. Develops and maintains an inventory monitoring system which allows for the preparation of all quality control materials and reagents as needed by the various operational Create and maintain records of preparation and perform validation of all quality control materials and reagents Assist Quality Manager and Laboratory Director in the design and implementation of an inspection ready lab system Assist with investigation of lot or quality control issues All functions outlined in Analys I. Additional Duties: Provides support for the department and assists with special projects, as assigned All other duties as assigned Education and Experience: Bachelor's degree, or higher, in medical technology, laboratory science, or one of the chemical, physical, or biological sciences [NY Only: qualifies as a clinical laboratory technologist] OR Associate degree in medical technology or one of the chemical, physical, or biological sciences [NY Only: qualifies as a clinical laboratory technician] One year experience as an Analyst I, II or III strongly preferred, not required. Related experience preferred, not required. Knowledge, Skills, and Abilities: Meticulous attention to detail Able to interpret and follow complex, written, technical instructions Sound technical ability & pipetting skills Ability to work independently Strong problem-solving skills Strong work ethic, punctual, reliable personal integrity and accountability High motivation level and detail oriented Personable and works well with team members Strong communication skills Understands and carries out instructions Promotes teamwork with a positive attitude and professional courtesy Physical Requirements: Light to moderate physical effort (lift/carry up to 25 lbs.) -Heavier weights with assistance Sitting & standing for long periods of time Repetitive motions and/or prolonged computer use Working at a fast pace, subject to many interruptions and both physical and mental stress

Job Title: QA Associate Reports To: Senior Manager, QA About Us: At Just-Evotec, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what's possible. We're on a mission to create a place where curiosity isn't just encouraged, it's celebrated. Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCureious with us and see where your curiosity can take you! The Role: We're looking for a passionate and curious QA Associate to join our team. If you're excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you'll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories. This role is responsible for the execution of day-to-day QA responsibilities for GMP manufacturing. This role works collaboratively with Manufacturing, Quality and Facilities staff to ensure compliance with cGMPs and internal procedures. The responsibilities of the employee is based on the assigned QA organization as outlined below. What You'll Do: Review executed Manufacturing Batch Records. Participate in compliance walkthrough of the Manufacturing floor and other assigned areas. Partner with Manufacturing to ensure compliance in Manufacturing operations. Review and approve Master Batch Records and other supporting documents. Execute process performance and product quality monitoring programs. Alert senior management of potential deviations or compliance risks. Initiate and review all quality events of eQMS (Deviations, Change Control, CAPA, Risk Assessment, Management Review, Complaint Investigation, Product Quality Review etc.) to assure compliance with regulatory and Just-Evotec Global Quality Management Systems (G-QMS) requirements. Provide input on communication as to the status of deliverables to customers, management, and stakeholders. Assist with developing training regarding QMS process or system changes. Support QA QMS in internal and external client audits and regulatory inspections (including but not limited to SME for QMS processes and individual records). Monitor effectiveness for QMS through trending, analysis, and metrics; report to top management and G-QMS on the performance of the KPIs and identify opportunities for continuous improvement. Lifecycle management of the stability program for clinical and commercial products Act as the QA representative on cross-functional product teams to integrate stability activities with project milestones. Support the design of stability protocols to ensure that they are aligned with program strategy and regulatory requirements. Ensure that stability studies are executed according to protocol. Review, verification, disposition, and archival of stability study data for assigned programs. Escalate unexpected data trends, OOS events, and risks appropriately, and drive/support resolution. Interpretate stability results to support expiry, trending, and conditions of products. Support product stability related content in regulatory submission, including responses to questions and post-marketing. Who You Are: Bachelor's Degree biological sciences, chemistry, biochemistry, engineering, or related life science field and 1 year of relevant quality experience OR Associate's degree and 3 years of relevant quality experience OR High school diploma / GED and 6 years of relevant quality experience. Strong attention to detail Ability to collaborate and communicate cross-functionally Why Join Us: Growth Opportunities: We're a company that believes in continuous learning and development. Whether it's professional courses, mentorship, or new projects, we'll help you grow. Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life (hybrid model). Inclusive Culture: We're committed to building a diverse and inclusive environment where everyone's voice is valued, and curiosity is encouraged. Innovative Projects: You'll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success. A Place for Big Ideas: We don't just talk about thinking outside the box, we throw the box away. If you've got ideas, we want to hear them. Are You Still Curious? If you've read this far, then chances are you've got a curious mind, just like us. So, what are you waiting for? Take the leap and apply today. We can't wait to see where your curiosity leads you, and how it will shape the future of Just-Evotec. Let your curiosity guide your career #BeCurious and explore the endless possibilities at Evotec! The base pay range for this position at commencement of employment is expected to be $65,000 to $90,000; Base salary offered may vary depending on the individual's skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits. Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.

Job Title: QA Associate Reports To: Senior Manager, QA About Us: At Just-Evotec, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what's possible. We're on a mission to create a place where curiosity isn't just encouraged, it's celebrated. Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCureious with us and see where your curiosity can take you! The Role: We're looking for a passionate and curious QA Associate to join our team. If you're excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you'll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories. This role is responsible for the execution of day-to-day QA responsibilities for GMP manufacturing. This role works collaboratively with Manufacturing, Quality and Facilities staff to ensure compliance with cGMPs and internal procedures. The responsibilities of the employee is based on the assigned QA organization as outlined below. What You'll Do: Review executed Manufacturing Batch Records. Participate in compliance walkthrough of the Manufacturing floor and other assigned areas. Partner with Manufacturing to ensure compliance in Manufacturing operations. Review and approve Master Batch Records and other supporting documents. Execute process performance and product quality monitoring programs. Alert senior management of potential deviations or compliance risks. Initiate and review all quality events of eQMS (Deviations, Change Control, CAPA, Risk Assessment, Management Review, Complaint Investigation, Product Quality Review etc.) to assure compliance with regulatory and Just-Evotec Global Quality Management Systems (G-QMS) requirements. Provide input on communication as to the status of deliverables to customers, management, and stakeholders. Assist with developing training regarding QMS process or system changes. Support QA QMS in internal and external client audits and regulatory inspections (including but not limited to SME for QMS processes and individual records). Monitor effectiveness for QMS through trending, analysis, and metrics; report to top management and G-QMS on the performance of the KPIs and identify opportunities for continuous improvement. Lifecycle management of the stability program for clinical and commercial products Act as the QA representative on cross-functional product teams to integrate stability activities with project milestones. Support the design of stability protocols to ensure that they are aligned with program strategy and regulatory requirements. Ensure that stability studies are executed according to protocol. Review, verification, disposition, and archival of stability study data for assigned programs. Escalate unexpected data trends, OOS events, and risks appropriately, and drive/support resolution. Interpretate stability results to support expiry, trending, and conditions of products. Support product stability related content in regulatory submission, including responses to questions and post-marketing. Who You Are: Bachelor's Degree biological sciences, chemistry, biochemistry, engineering, or related life science field and 1 year of relevant quality experience OR Associate's degree and 3 years of relevant quality experience OR High school diploma / GED and 6 years of relevant quality experience. Strong attention to detail Ability to collaborate and communicate cross-functionally Why Join Us: Growth Opportunities: We're a company that believes in continuous learning and development. Whether it's professional courses, mentorship, or new projects, we'll help you grow. Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life (hybrid model). Inclusive Culture: We're committed to building a diverse and inclusive environment where everyone's voice is valued, and curiosity is encouraged. Innovative Projects: You'll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success. A Place for Big Ideas: We don't just talk about thinking outside the box, we throw the box away. If you've got ideas, we want to hear them. Are You Still Curious? If you've read this far, then chances are you've got a curious mind, just like us. So, what are you waiting for? Take the leap and apply today. We can't wait to see where your curiosity leads you, and how it will shape the future of Just-Evotec. Let your curiosity guide your career #BeCurious and explore the endless possibilities at Evotec! The base pay range for this position at commencement of employment is expected to be $65,000 to $90,000; Base salary offered may vary depending on the individual's skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits. Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.

Job Description A successful biotech company is looking for an experienced and detail-oriented Associate to join our Quality Assurance team on site in Bothell, WA. Unfortunately at this time no relocation or visa sponsorship provided. At ELITechGroup, we are committed to supporting health systems globally. We take pride in our team and strive to maintain a work environment that is both professionally challenging and personally fulfilling. As a valued member of our team, you would contribute to the manufacturing and distribution of in vitro diagnostic products to clients in over 100 countries. You will have the opportunity to work alongside some of the brightest minds in the industry, as our team is dedicated to solving problems and delivering excellent products. This position is ideal for someone with some experience in the biotech industry and audits, who takes pride in learning all aspects of the job and adhering to procedures and standards. You will receive guidance from a supportive team that will ensure you are trained and capable of performing your responsibilities effectively. The primary focus of the QA Associate role is to support commercial production to ensure consistent compliance with regulatory and industry expectations. Assist the QA department in maintaining the Quality focused culture by ensuring documentation is complete, accurate and that Batch records are executed in accordance with approved and effective standard operating procedures and specifications. Summary With direction, has part of the responsibility for ELITechGroup MDx Quality Assurance activities. Essential Duties and Responsibilities Performs review of manufacturing batch records, enter information in Disposition Log, filing of batch records, and ensure the records are complete and stored in a manner where they are readily retrievable. Performs finished product inspection. Performs review and approval of labels. Reviews SPEC sheets, enter information in Disposition Log, file. Assists QA with the tracking and/or completion of CAPAs and Customer Complaints. Assists QA with the tracking and/or completion of NCRs, OOSs, TMPs. Assigns part numbers. Reviews, tracks, and files training forms. Ensures the training log is updated. Reviews calibration/maintenance records, update tracking log, file. Ensure the records are complete and stored in a manner where they are readily retrievable. Participates during audits (FDA, ISO, vendor) Assists Document Control, (assign CC and document numbers, assist in obtaining approvals, auditing external documents, etc.) when necessary. Other duties and task as assigned. Competencies To perform the job successfully, an individual should demonstrate the following competencies: Organizational Support - follows policies and procedures; completes administrative tasks correctly and on time; supports organization's goals and values. Quality - Demonstrates accuracy and thoroughness; monitors own work to ensure quality. Written Communication - writes clearly and informatively; able to read and interpret written information. Qualifications The requirements listed below are representative of the knowledge, skill, and/or ability required. Bachelor's degree (B.A. or B.S.), or equivalent combination of education and experience. Minimum of 2 years' experience in working in an FDA or ISO regulated environment or equivalent training. Knowledge of ISO 13485, ISO 9001, and FDA QSR preferred Job Posted by ApplicantPro

JOB DETAILS Base Pay: $23.50 - $25.50 per hour Shift: Day Shift, 6:00 AM - 6:30 PM Shoe Voucher/Reimbursement DUTIES AND RESPONSIBILITIES The Quality Assurance Technician in the Extrusion department ensures that all vinyl profiles produced for window manufacturing meet strict quality standards. This role is responsible for inspecting materials and finished products, performing tests, analyzing data, and working closely with production and engineering teams to resolve quality issues. The QA Technician is critical to maintaining compliance with industry standards and supporting the company's continuous improvement initiatives in vinyl extrusion processes. Inspect vinyl profiles for dimensional accuracy, surface quality, and consistency according to product specifications Conduct regular in-process and final product quality checks, using precision measuring tools (e.g., calipers, micrometers, gauges) Perform material testing on vinyl, including tensile strength, UV resistance, and impact testing, ensuring compliance with industry standards Monitor extrusion lines to ensure consistent quality output, identifying and correcting any deviations from standards Document and analyze quality data using statistical process control (SPC) techniques, presenting findings to management Collaborate with production and engineering teams to identify root causes of defects and develop corrective actions · Maintain up-to-date quality records, including test results, inspection logs, and production reports Participate in process audits and contribute to continuous improvement efforts for optimizing the extrusion process Assist with maintaining and improving the company's quality management system (QMS) in compliance with ISO 9001 or other relevant standards Ensure that all products meet safety, regulatory, and customer specifications before shipment Qualifications High school diploma or equivalent Associate degree or technical diploma in manufacturing, engineering, or a related field (preferred) Certification in quality control (e.g., Certified Quality Technician, Six Sigma certification) is a plus 1-3 years of experience in quality control/assurance in a manufacturing environment, preferably in vinyl extrusion or window manufacturing Familiarity with extrusion processes, vinyl materials, and window profile standards Experience with statistical process control (SPC) and data analysis tools in a manufacturing setting Proficiency in using precision measuring tools such as micrometers, calipers, and gauges for product inspection Familiarity with ISO standards (e.g., ISO 9001) and quality management systems (QMS) Understanding of material properties related to vinyl, including UV and thermal resistance Experience with blueprint reading, including specifications for window profiles and dimensions Proficiency with quality control software and data entry tools Attention to Detail: Ability to identify defects such as surface imperfections, incorrect dimensions, or inconsistencies in vinyl profiles Problem-Solving: Strong analytical skills for identifying root causes of quality issues and developing corrective measures Communication: Ability to communicate findings clearly and work effectively with production, engineering, and quality teams Data Analysis: Ability to collect, interpret, and present quality data to support decision-making Time Management: Ability to prioritize tasks and maintain efficiency in a fast-paced manufacturing environment Computer Skills: Basic knowledge of Microsoft Office (Word, Excel, Outlook) for reporting and documentation purposes Ability to stand for extended periods and lift items up to 50 lbs Comfortable working in a manufacturing floor environment with exposure to noise, heat, and moving machinery Additional Information Site Address: 5001 D Street NW Auburn, WA, 98001 All your information will be kept confidential according to EEO guidelines. Why work for Cornerstone Building Brands? Our teams are at the heart of our purpose to positively contribute to the communities where we live, work and play . Full-time* team members receive** medical, dental and vision benefits starting day 1. Other benefits include PTO, paid holidays, FSA, life insurance, LTD, STD, 401k, EAP, discount programs, tuition reimbursement, training, and professional development. *Full-time is defined as regularly working 30+ hours per week. **Union programs may vary depending on the collective bargaining agreement. Cornerstone Building Brands is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, or status as a protected veteran. You can find the Equal Employment Opportunity Poster here . You can also view Your Right to Work Poster here along with This Organizations Participation in E-Verify Poster here . If you'd like to view a copy of the company's affirmative action plan for protected veterans or individuals with disabilities or policy statement, please contact Human Resources at ************ or [email protected] . If you have a disability and you believe that you need a reasonable accommodation in order to search for a job opening or to submit an online application, please contact Human Resources at ************ or [email protected] . This email is used exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only emails received for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response. All your information will be kept confidential according to EEO guidelines. California Consumer Privacy Act (CCPA) of 2018 Must be at least 18 years of age to apply. Notice of Recruitment Fraud We have been made aware of multiple scams whereby unauthorized individuals are using Cornerstone Building Brand's name and logo to solicit potential job-seekers for employment. In some cases, job-seekers are being contacted directly, both by phone and e-mail. In other instances, these unauthorized individuals are placing advertisements for fake positions with both legitimate websites and fabricated ones. These individuals are typically promising high-paying jobs with the requirement that the job-seeker send money to pay for things such as visa applications or processing fees. Please be advised that Cornerstone Building Brands will never ask potential job-seekers for any sort of advance payment or bank account information as part of the recruiting or hiring process.

Job DescriptionSalary: Hourly DOE Job Title: Quality Control Technician Reports To:Quality Assurance Manager Job Type:Full-Time - Wed to Sat 7am to 5:30pm Join our team at a SQF Certified food manufacturing facility, where we are dedicated to producing high-quality products in a safe and compliant environment. We offer a competitive salary, comprehensive health benefits, and paid vacation. Position Overview: The Quality Control (QC) Technician ensures that all products meet safety and quality standards as required by food safety regulations and company policies. This role will be responsible for conducting inspections, performing tests, and maintaining records to ensure that our products consistently meet the highest standards for quality and safety. Key Responsibilities: Conduct regular quality checks on raw materials, in-process products, and finished goods in accordance with established standards. Perform routine inspections of equipment, processes, and packaging to ensure compliance with SQF standards and internal procedures. Document and maintain accurate records of inspections, tests, and findings in compliance with food safety regulations and internal policies. Assist in identifying and reporting any non-conformities in the production process and follow up on corrective actions. Support the development and implementation of food safety and quality programs, including HACCP, GMP, and SQF certifications. Monitor sanitation processes and ensure adherence to hygiene standards across production areas. Conduct environmental sampling and microbial testing as needed. Assist in training production staff in quality control procedures and food safety practices. Collaborate with the Quality Assurance team to ensure all quality systems are maintained and updated. Assist in audits, both internal and external, and ensure continuous improvement of quality systems. Qualifications: High school diploma or equivalent; an associates degree or certification in Food Science, Microbiology, or a related field is preferred. 1-2 years of experience in a quality control or food safety role, preferably in a food manufacturing environment. Knowledge of SQF, HACCP, and GMPs is highly desirable. Strong attention to detail and ability to follow procedures meticulously. Excellent communication and problem-solving skills. Ability to work independently and as part of a team. Proficiency in Microsoft Office Suite (Word, Excel, Outlook). Benefits: Competitive salary based on experience. Health benefits, including medical, dental, and vision. Paid vacation and holidays. Opportunities for professional growth and advancement. How to Apply: Interested candidates should submit their resume. We are an equal opportunity employer and value diversity in our workplace. About Promise Confections At Promise Confections, we take immense pride in being an award-winning manufacturer of everyday chocolate and confectionery products. Our commitment is to continually challenge the norms of traditional confectionery, pushing boundaries to deliver exceptional experiences. Comprising Edward Marc Brands, Seattle Gourmet Foods, Pearsons Candy Co., and Annabelle Candy Co., we boast a diverse range of capabilities including panning, enrobing, extruding, clusters, barks, brittles, gummies and breath mint/sour candy tableting. With our extensive reach, servicing major retailers and offering private label and contract manufacturing services, we stand as emerging industry disrupters in confectionery. Check out our brands by visiting: promiseconfections.com

In this role, you will be responsible for the preparation and review of required procedures, documentation, and retention practices, supporting inspections, and promoting continuous improvement and compliance efforts. You will support global operations across PharmSci and partner lines to align goals and implement effective quality system solutions. Your collaboration and implementation of practices will enhance efficiencies throughout quality procedures and documentation. Your contributions will be vital in achieving team goals and ensuring timely completion of important deliverables. Your innovative communication skills will facilitate consensus between teams, ultimately enabling customers and patients to receive the medicines they need when they need them. Responsibilities * Perform procedural administration activities within the Global Documentation Management System. * Collaborate with PharmSci and PGS business lines to develop, implement, and manage procedures, documentation, and records. * Support management of Active libraries and other documentation systems to ensure control of physical and electronic records. * Manage inventory of records within the Central Index of Company Records (CICR) system for record creation, management, retention, and disposal. * Partner with the Enterprise Records and Information Management (eRIM) team to align with record retention policies and legal holds. * Collaborate with off-site teams to manage the lifecycle of company records and ensure retrieval processes for audits and inspections. * Provide technical writing, editing, and design support to team members and site departments. * Work closely with project teams to ensure documents are accurate, consistent, and compliant with internal standards and regulatory guidelines. * Support equipment change controls, manage calibration/PM schedules, and coordinate associated documentation. Essential Skills * 1+ years of experience. * Understanding of cGMP, Data Integrity, and ALCOA principles. * Strong organizational and communication skills. * Proficiency in word processing and document formatting. * Expertise in Microsoft Office applications (Word, Excel, PowerPoint, Visio). Additional Skills & Qualifications * Relevant pharmaceutical experience. * Demonstrated technical writing experience is desirable. * Strong project management skills. Work Environment The role involves collaborating with various teams and managing documentation systems within a structured environment. Familiarity with technologies such as electronic document management systems (EDMS) and adherence to FDA regulations are important. The work involves both physical and electronic documentation management, requiring attention to detail and organizational skills. We reserve the right to pay above or below the posted wage based on factors unrelated to sex, race, or any other protected classification. 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. This temporary role may be eligible for the following: * Medical, dental & vision * 401(k)/Roth * Insurance (Basic/Supplemental Life & AD&D) * Short and long-term disability * Health & Dependent Care Spending Accounts (HSA & DCFSA) * Transportation benefits * Employee Assistance Program .Time Off/Leave (PTO, Vacation or Sick Leave) Job Type & Location This is a Contract position based out of Bothell, WA. Pay and Benefits The pay range for this position is $24.00 - $28.00/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 Bothell,WA. Application Deadline This position is anticipated to close on Jan 20, 2026. About Actalent 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 actalentaccommodation@actalentservices.com for other accommodation options.

Quality Control Technician Department: Operations FLSA Status: Non-exempt Reports to: Quality Assurance Manager Travel: 0-5% About the Position Position Description: The Quality Control Technician I is responsible for inspecting and testing of our products to ensure conformance with Bodypoints standards and design specifications. The position will be required to report their inspection results based upon routine physical and analytical testing; visual inspection; first part evaluations; and tests as needed for failure analysis. Also, the role will be responsible for recording accurate Quality Control records data and recommend/appropriate data-driven action. Maintains calibration of all inspection and production tools, equipment, and gages. \ 1.1 Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Performs routine measurements, inspection, and gaging as defined by part standards for incoming and production materials and parts Report any non-conformances and seek assistance with the Quality Manager to analyze data Does in-process check per part runs on shop floor by required Standard Operation Procedures (SOPs) Collaborates with Lead inspectors and production staff with quality assurance procedures Records measurement data into Unipoint and Syspro database(s) Extrapolates test data and presents information via charts or graphs. Communicates Quality issues to appropriate personnel Verifies that product meets pre-determined manufacturer s Performs receiving inspection per receiving details in Syspro Reviews MRB (Material Review Board) area for any incoming non-conformance and places holds accordingly Other duties, responsibilities, and activities may change or be assigned at any time with or without notice. 1.2 Supervisory Duties and Responsibilities: This position has no supervisory responsibilities. POSITION requirements Required Education or Experience: Minimum of high school diploma or equivalent. 3 or more years of experience in Quality Assurance Ability to read blueprints Certificates, Licenses, or Registrations: Certificate in Metrology preferred American Society of Quality Certification or Certificate in Quality Management Systems preferred 2.2 Required Skills: Computer proficient with Microsoft Office. Experience with UniPoint, and specialized equipment software preferred. Teamwork ability to work with others supporting Bodypoints Values and Principles (Quality, Integrity, Caring). Self-directed complete job duties with minimal supervision. Mechanical effectively use tools and equipment to perform job duties. Communication effectively communicate with peers and managers verbally and in writing. Problem solving able to diagnose complex equipment problems and determine solutions and opportunities for improvement. 2.3 Physical Activities and Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Sitting, standing, bending, reaching, pulling / pushing, kneeling, twisting, grasping, and walking. Moderate moving, transporting and positioning of items weighing up to 50 lbs. Work environment 3.0 Work Location Type: Indoor facility, manufacturing environment, location WA State. Frequently remaining in a stationary position, often standing or sitting for prolonged periods. Occasionally walking, bending, and lifting items up to 50lbs. 3.1 Environmental Conditions: While performing the duties of this job, the employee works around running machines and equipment. The employee is exposed to minimal noise levels in the work environment. The employee may be infrequently exposed to hazardous and non-caustic chemicals or solutions. Bodypoint provides appropriate PPE for working conditions and environment. Nothing in this job description restricts managements right to assign or reassign duties and responsibilities to this job at any time. Bodypoint believes that each employee makes a significant contribution to our success. That contribution should not be limited by the assigned responsibilities. This position description is designed to outline primary duties, qualifications, and job scope, but not limit our employees nor the organization to just the work identified. It is our expectation that each employee will offer their services wherever and whenever necessary to ensure the success of the organization.

To perform all aspects of final quality control within the Finish Dept. Formally responsible for providing input for improvements. Deciding whether material meets quality standards. Deciding when to repair or replace defective product. No formal supervisory responsibility. Job Profile Attendance and punctuality that meets PCI standards. Performs work and manages work group in a manner that complies with the company's safety policies, this includes housekeeping, organization, and PPE. Conducts themselves in a manner that falls in line with PCI's core values. Essential Responsibilities Performs the required amount of work that will enable the team to meet weekly Finish dept. productivity requirements. Performs work in accordance with Finish dept. quality standards. This includes: All finish parts, doors and accessories matching master samples, proper part handling, proper topcoat coverage, and no vortexing. Ensure all parts are accounted for before they are sent to Assembly or Accessory wrap. Assists other areas or departments as necessary. Qualifications Oral and written communication skills. Read and understand a tape measure. Basic Math skills. High school diploma or equivalent.

A successful biotech company is looking for an experienced and detail-oriented Associate to join our Quality Assurance team on site in Bothell, WA. Unfortunately at this time no relocation or visa sponsorship provided. At ELITechGroup, we are committed to supporting health systems globally. We take pride in our team and strive to maintain a work environment that is both professionally challenging and personally fulfilling. As a valued member of our team, you would contribute to the manufacturing and distribution of in vitro diagnostic products to clients in over 100 countries. You will have the opportunity to work alongside some of the brightest minds in the industry, as our team is dedicated to solving problems and delivering excellent products. This position is ideal for someone with some experience in the biotech industry and audits, who takes pride in learning all aspects of the job and adhering to procedures and standards. You will receive guidance from a supportive team that will ensure you are trained and capable of performing your responsibilities effectively. The primary focus of the QA Associate role is to support commercial production to ensure consistent compliance with regulatory and industry expectations. Assist the QA department in maintaining the Quality focused culture by ensuring documentation is complete, accurate and that Batch records are executed in accordance with approved and effective standard operating procedures and specifications. Summary With direction, has part of the responsibility for ELITechGroup MDx Quality Assurance activities. Essential Duties and Responsibilities * Performs review of manufacturing batch records, enter information in Disposition Log, filing of batch records, and ensure the records are complete and stored in a manner where they are readily retrievable. * Performs finished product inspection. * Performs review and approval of labels. * Reviews SPEC sheets, enter information in Disposition Log, file. * Assists QA with the tracking and/or completion of CAPAs and Customer Complaints. * Assists QA with the tracking and/or completion of NCRs, OOSs, TMPs. * Assigns part numbers. * Reviews, tracks, and files training forms. Ensures the training log is updated. * Reviews calibration/maintenance records, update tracking log, file. * Ensure the records are complete and stored in a manner where they are readily retrievable. * Participates during audits (FDA, ISO, vendor) * Assists Document Control, (assign CC and document numbers, assist in obtaining approvals, auditing external documents, etc.) when necessary. * Other duties and task as assigned. Competencies To perform the job successfully, an individual should demonstrate the following competencies: Organizational Support - follows policies and procedures; completes administrative tasks correctly and on time; supports organization's goals and values. Quality - Demonstrates accuracy and thoroughness; monitors own work to ensure quality. Written Communication - writes clearly and informatively; able to read and interpret written information. Qualifications The requirements listed below are representative of the knowledge, skill, and/or ability required. * Bachelor's degree (B.A. or B.S.), or equivalent combination of education and experience. * Minimum of 2 years' experience in working in an FDA or ISO regulated environment or equivalent training. * Knowledge of ISO 13485, ISO 9001, and FDA QSR preferred

A successful biotech company is looking for an experienced and detail-oriented Associate to join our Quality Assurance team on site in Bothell, WA. Unfortunately at this time no relocation or visa sponsorship provided. At ELITechGroup, we are committed to supporting health systems globally. We take pride in our team and strive to maintain a work environment that is both professionally challenging and personally fulfilling. As a valued member of our team, you would contribute to the manufacturing and distribution of in vitro diagnostic products to clients in over 100 countries. You will have the opportunity to work alongside some of the brightest minds in the industry, as our team is dedicated to solving problems and delivering excellent products. This position is ideal for someone with some experience in the biotech industry and audits, who takes pride in learning all aspects of the job and adhering to procedures and standards. You will receive guidance from a supportive team that will ensure you are trained and capable of performing your responsibilities effectively. The primary focus of the QA Associate role is to support commercial production to ensure consistent compliance with regulatory and industry expectations. Assist the QA department in maintaining the Quality focused culture by ensuring documentation is complete, accurate and that Batch records are executed in accordance with approved and effective standard operating procedures and specifications. Summary With direction, has part of the responsibility for ELITechGroup MDx Quality Assurance activities. Essential Duties and Responsibilities Performs review of manufacturing batch records, enter information in Disposition Log, filing of batch records, and ensure the records are complete and stored in a manner where they are readily retrievable. Performs finished product inspection. Performs review and approval of labels. Reviews SPEC sheets, enter information in Disposition Log, file. Assists QA with the tracking and/or completion of CAPAs and Customer Complaints. Assists QA with the tracking and/or completion of NCRs, OOSs, TMPs. Assigns part numbers. Reviews, tracks, and files training forms. Ensures the training log is updated. Reviews calibration/maintenance records, update tracking log, file. Ensure the records are complete and stored in a manner where they are readily retrievable. Participates during audits (FDA, ISO, vendor) Assists Document Control, (assign CC and document numbers, assist in obtaining approvals, auditing external documents, etc.) when necessary. Other duties and task as assigned. Competencies To perform the job successfully, an individual should demonstrate the following competencies: Organizational Support - follows policies and procedures; completes administrative tasks correctly and on time; supports organization's goals and values. Quality - Demonstrates accuracy and thoroughness; monitors own work to ensure quality. Written Communication - writes clearly and informatively; able to read and interpret written information. Qualifications The requirements listed below are representative of the knowledge, skill, and/or ability required. Bachelor's degree (B.A. or B.S.), or equivalent combination of education and experience. Minimum of 2 years' experience in working in an FDA or ISO regulated environment or equivalent training. Knowledge of ISO 13485, ISO 9001, and FDA QSR preferred

JOB DETAILS Base Pay: $23.50 - $25.50 per hour Shift: Day Shift, 6:00 AM - 6:30 PM Shoe Voucher/Reimbursement DUTIES AND RESPONSIBILITIES The Quality Assurance Technician in the Extrusion department ensures that all vinyl profiles produced for window manufacturing meet strict quality standards. This role is responsible for inspecting materials and finished products, performing tests, analyzing data, and working closely with production and engineering teams to resolve quality issues. The QA Technician is critical to maintaining compliance with industry standards and supporting the company's continuous improvement initiatives in vinyl extrusion processes. * Inspect vinyl profiles for dimensional accuracy, surface quality, and consistency according to product specifications * Conduct regular in-process and final product quality checks, using precision measuring tools (e.g., calipers, micrometers, gauges) * Perform material testing on vinyl, including tensile strength, UV resistance, and impact testing, ensuring compliance with industry standards * Monitor extrusion lines to ensure consistent quality output, identifying and correcting any deviations from standards * Document and analyze quality data using statistical process control (SPC) techniques, presenting findings to management * Collaborate with production and engineering teams to identify root causes of defects and develop corrective actions * · Maintain up-to-date quality records, including test results, inspection logs, and production reports * Participate in process audits and contribute to continuous improvement efforts for optimizing the extrusion process * Assist with maintaining and improving the company's quality management system (QMS) in compliance with ISO 9001 or other relevant standards * Ensure that all products meet safety, regulatory, and customer specifications before shipment Qualifications * High school diploma or equivalent * Associate degree or technical diploma in manufacturing, engineering, or a related field (preferred) * Certification in quality control (e.g., Certified Quality Technician, Six Sigma certification) is a plus * 1-3 years of experience in quality control/assurance in a manufacturing environment, preferably in vinyl extrusion or window manufacturing * Familiarity with extrusion processes, vinyl materials, and window profile standards Experience with statistical process control (SPC) and data analysis tools in a manufacturing setting * Proficiency in using precision measuring tools such as micrometers, calipers, and gauges for product inspection * Familiarity with ISO standards (e.g., ISO 9001) and quality management systems (QMS) * Understanding of material properties related to vinyl, including UV and thermal resistance * Experience with blueprint reading, including specifications for window profiles and dimensions * Proficiency with quality control software and data entry tools * Attention to Detail: Ability to identify defects such as surface imperfections, incorrect dimensions, or inconsistencies in vinyl profiles * Problem-Solving: Strong analytical skills for identifying root causes of quality issues and developing corrective measures * Communication: Ability to communicate findings clearly and work effectively with production, engineering, and quality teams * Data Analysis: Ability to collect, interpret, and present quality data to support decision-making * Time Management: Ability to prioritize tasks and maintain efficiency in a fast-paced manufacturing environment * Computer Skills: Basic knowledge of Microsoft Office (Word, Excel, Outlook) for reporting and documentation purposes * Ability to stand for extended periods and lift items up to 50 lbs * Comfortable working in a manufacturing floor environment with exposure to noise, heat, and moving machinery Additional Information Site Address: 5001 D Street NW Auburn, WA, 98001 All your information will be kept confidential according to EEO guidelines. Why work for Cornerstone Building Brands? Our teams are at the heart of our purpose to positively contribute to the communities where we live, work and play. Full-time* team members receive medical, dental and vision benefits starting day 1. Other benefits include PTO, paid holidays, FSA, life insurance, LTD, STD, 401k, EAP, discount programs, tuition reimbursement, training, and professional development. * Full-time is defined as regularly working 30+ hours per week. Union programs may vary depending on the collective bargaining agreement. Cornerstone Building Brands is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, or status as a protected veteran. You can find the Equal Employment Opportunity Poster here. You can also view Your Right to Work Poster here along with This Organizations Participation in E-Verify Poster here. If you'd like to view a copy of the company's affirmative action plan for protected veterans or individuals with disabilities or policy statement, please contact Human Resources at ************ or *******************************. If you have a disability and you believe that you need a reasonable accommodation in order to search for a job opening or to submit an online application, please contact Human Resources at ************ or *******************************. This email is used exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only emails received for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response. All your information will be kept confidential according to EEO guidelines. California Consumer Privacy Act (CCPA) of 2018 Must be at least 18 years of age to apply. Notice of Recruitment Fraud We have been made aware of multiple scams whereby unauthorized individuals are using Cornerstone Building Brand's name and logo to solicit potential job-seekers for employment. In some cases, job-seekers are being contacted directly, both by phone and e-mail. In other instances, these unauthorized individuals are placing advertisements for fake positions with both legitimate websites and fabricated ones. These individuals are typically promising high-paying jobs with the requirement that the job-seeker send money to pay for things such as visa applications or processing fees. Please be advised that Cornerstone Building Brands will never ask potential job-seekers for any sort of advance payment or bank account information as part of the recruiting or hiring process.

Job DescriptionQuality Technician IIRapidly Growing Renewable Energy Company Seattle Area/Relocation Assistance Available$26 per hour, with potential flexibility based on experience Terrific Quality Technician position with a rapidly growing renewable energy company. The position will ensure quality and compliance for products and services manufactured. Previous quality control experience in a fast paced production environment is essential for this role.Responsibilities: Ensure production lines adhere to and comply with legal requirements, standards, and procedures Provide training to productions teams to improve quality control and product excellence Review and interpret blueprints, drawings, and radiographs Perform testing on the production line and propose improvements Collect quality data and provide statistical analysis reports Monitor operations and suggest improvements to processes Qualifications: Prior experience in a fast paced production environment Manufacturing experience within a technical role, experience with PV module is preferred Strong problem solving skills Tech savvy Ability to work collaboratively in a team environment and also independently Equal opportunity employer

In this role, you will be responsible for the preparation and review of required procedures, documentation, and retention practices, supporting inspections, and promoting continuous improvement and compliance efforts. You will support global operations across PharmSci and partner lines to align goals and implement effective quality system solutions. Your collaboration and implementation of practices will enhance efficiencies throughout quality procedures and documentation. Your contributions will be vital in achieving team goals and ensuring timely completion of important deliverables. Your innovative communication skills will facilitate consensus between teams, ultimately enabling customers and patients to receive the medicines they need when they need them. Responsibilities * Perform procedural administration activities within the Global Documentation Management System. * Collaborate with PharmSci and PGS business lines to develop, implement, and manage procedures, documentation, and records. * Support management of Active libraries and other documentation systems to ensure control of physical and electronic records. * Manage inventory of records within the Central Index of Company Records (CICR) system for record creation, management, retention, and disposal. * Partner with the Enterprise Records and Information Management (eRIM) team to align with record retention policies and legal holds. * Collaborate with off-site teams to manage the lifecycle of company records and ensure retrieval processes for audits and inspections. * Provide technical writing, editing, and design support to team members and site departments. * Work closely with project teams to ensure documents are accurate, consistent, and compliant with internal standards and regulatory guidelines. * Support equipment change controls, manage calibration/PM schedules, and coordinate associated documentation. Essential Skills * 1+ years of experience. * Understanding of cGMP, Data Integrity, and ALCOA principles. * Strong organizational and communication skills. * Proficiency in word processing and document formatting. * Expertise in Microsoft Office applications (Word, Excel, PowerPoint, Visio). Additional Skills & Qualifications * Relevant pharmaceutical experience. * Demonstrated technical writing experience is desirable. * Strong project management skills. Work Environment The role involves collaborating with various teams and managing documentation systems within a structured environment. Familiarity with technologies such as electronic document management systems (EDMS) and adherence to FDA regulations are important. The work involves both physical and electronic documentation management, requiring attention to detail and organizational skills. We reserve the right to pay above or below the posted wage based on factors unrelated to sex, race, or any other protected classification. 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. This temporary role may be eligible for the following: * Medical, dental & vision * 401(k)/Roth * Insurance (Basic/Supplemental Life & AD&D) * Short and long-term disability * Health & Dependent Care Spending Accounts (HSA & DCFSA) * Transportation benefits * Employee Assistance Program .Time Off/Leave (PTO, Vacation or Sick Leave) Job Type & Location This is a Contract position based out of Bothell, WA. Pay and Benefits The pay range for this position is $24.00 - $28.00/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 Bothell,WA. Application Deadline This position is anticipated to close on Jan 19, 2026. About Actalent 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 actalentaccommodation@actalentservices.com for other accommodation options.