Quality Control Internship jobs at HNTB

About the Role We're seeking creative, detail-oriented AI Image Generator / AI QC Specialist contractors to join a cutting-edge content studio in Brooklyn that's redefining food, drink, and lifestyle visuals through AI-driven image generation and hybrid photography workflows. This team produces hundreds of food and drink visuals weekly, blending AI-generated imagery with traditional photography to deliver high-quality, engaging content. Do you have this type of experience? If so, keep reading! Location: Hybrid, Brooklyn (2 days onsite per week) Schedule: ~32 hours/week (4 days) Rate: $40/hour W2 Duration: 3 months (with potential extension) Start Date: ASAP AI Image Generator / AI QC Specialist Responsibilities AI Prompting & Image Generation... Use generative AI tools (e.g., Midjourney, Stable Diffusion, DALL·E, etc.) to create food and lifestyle visuals. Experiment with prompt engineering to achieve brand-consistent aesthetics. Quality Control & Refinement... Review AI outputs for accuracy, realism, and visual appeal. Perform retouching and enhancements in Adobe Photoshop or similar tools. Ensure color consistency, composition quality, and adherence to brand guidelines. Collaboration... Work closely with photographers and creative leads to integrate AI-generated elements into hybrid compositions. Provide feedback on image selection and creative direction. Assist with image metadata tagging for asset management. Support basic layout design for recipe cards and social media content. Stay updated on emerging AI tools and techniques to improve workflow efficiency. AI Image Generator / AI QC Specialist Qualifications Experience with generative AI platforms and prompts (Midjourney, Gemini, Nano Banana, Stable Diffusion, DALL·E, Firefly, etc.). Strong Photoshop skills for retouching and compositing where needed with the AI output. Eye for detail and ability to maintain visual consistency across large volumes of content. Basic understanding of food styling and photography principles is a plus. Comfortable working in a fast-paced, high-output environment. Why Join? This is an opportunity to work at the forefront of AI-powered creative production, gain hands-on experience with cutting-edge tools, and collaborate with a team shaping the future of visual content. No deadline to apply.

Responsibilities Strong skills in test planning and traceability for compliance and audit purposes. Lead with curiosity to further requirements discussions and uncover test scenarios. Review requirements and specifications to ensure testability. Ability to identify critical business workflows and ensure they remain intact after changes. Develop and maintain manual test cases based on functional requirements and acceptance criteria. Execute manual tests and document results. Log and track defects using appropriate tools. Perform regression testing after bug fixes and new feature deployments. Collaborate with developers, product owners, and other stakeholders to clarify requirements. Participate in test planning and estimation. Ensure quality standards are met before release. Provide clear and detailed defect reports and communicate effectively with the team. Contribute to continuous improvement of Agile and QA processes. Required Skills Strong understanding of software testing methodologies (functional, regression, smoke). Ability to create, execute, and maintain test cases and test plans. Familiarity with bug tracking tools (Azure DevOps, Jira). Strong knowledge of SDLC and Agile methodologies. Strong analytical and problem-solving skills. Excellent written and verbal communication for reporting defects and collaborating with teams. Ability to ask 'Why' and 'What If' questions to enhance discussion and discovery. Attention to detail and ability to identify edge cases. Hands on experience with API testing (using tools like Postman is a plus). Hands on experience with SQL and database queries. Experience with large-scale regression suites. Ability to prioritize test cases for high-risk areas. Knowledge of impact analysis for upgrades and migrations. Ability to coach others and create a testing mindset. Ability to work in a team environment. Ability to self-organize and prioritize tasks within multiple teams. Preferred Skills Knowledge of version control systems (e.g., Git). Understanding of server architecture (Windows). Familiarity with cloud platforms (Azure). Ability to validate configuration changes and deployment impacts. Awareness of test automation frameworks (Selenium, Cypress, Playwright) - even if not hands-on yet. Ability to learn and adapt to automation tools and scripting. Strong analytical thinking for identifying automation opportunities. Education Bachelor's degree in Computer Science, Information Technology, or related field. Equivalent experience in QA/testing may be considered in lieu of formal education. Certifications (Preferred but not mandatory) ISTQB Foundation Level (preferred) Any Agile or Scrum certification (e.g., Certified Scrum Tester). Experience 4+ years of experience

We're hiring for a Quality Technician role onsite in Rochester, New York. In collaboration with process engineering, system design engineering and business development, the QC Technician (QCT) is involved in the inspection of customer samples, prototypes, and products for printed electronics applications. This is a position requiring flexibility, versatility, technical aptitude and attention to detail. Our Printed Electronics organization uses production-scale assets and processes for both development and production work. Processes include flexographic printing, electroless plating, end-of-line testing and packaging. The QCT will be cross trained on all inspection equipment and is expected to develop sufficient mastery for independent work in all aspects of the quality assurance process flow. Up to 25% of time is spent in either a Class 6 or 7 clean room, with the remaining time spent in a QC lab or office environment. Responsibilities: • Interpret instructions and execute work orders utilizing inspection equipment. • Collaborate with peers and team leaders to accomplish major objectives for the day while balancing workload, rotating job assignments, and completing routine tasks that are documented but not otherwise specified by supervision. • Inspection and quality assessment of incoming materials, WIP and product. • Identify problem conditions (Product, Process and/or general) and escalate to the appropriate supervision. • Perform routine cleaning and minor maintenance of inspection assets. • As needed, write and maintain standard operating procedures either independently or in collaboration with process engineering. • Routinely learn new tasks and adapt to new processes. • Comply with ISO 9001 and IATF 16949 Quality Management System requirements. • Sample management, Deviation Report (DR) reporting, Microscopy and Visual Inspection. • Backup and support for other QC roles within the organization, including chemical handling and analysis. Required Skills: • Operate measurement equipment in Class 6 & 7 cleanrooms with full head-to-toe gowning and adherence to clean room protocols. • Ability to visually inspect and detect defects in production and incoming materials. • Proficient in basic math functions and computer skills, including navigating screens, data entry, and email. • Work effectively with minimal supervision. • Ability to prioritize work to meet business needs. • Express oneself and communicate clearly, both written and verbal, and comprehend a variety of work requests. • Maintain a clean work area. • Maintain strict adherence to safety procedures and quality standards. • Dependable, maintain good attendance. Desired Skills: • Experience working in a clean room environment. • Experience in quality control role supporting production; including inspections and certification of incoming materials, WIP, product and post-production audit sampling. • Familiarity with FMEA (Failure Mode Effects Analysis) processes. • Experience with microscopy. • Experience with chemical handling. • Flexographic printing experience. • Internal Audit experience to ISO 9001. • Familiar with Statistical Process Control (SPC) . • Ability to read drawings including GD&T (Geometric Dimensioning & Tolerancing.

Our client, a global leader in the pharmaceutical manufacturing industry, is seeking a QC Analyst to join their team! - Pay: $25-30/hr ($25/hr for entry level/recent graduate) - Shift: 1st shift M-F GENERAL DESCRIPTION: The QC Analyst I performs testing of samples submitted to the laboratory in a cGMP compliant manner, as well as according to approved written procedures. The QC Analyst I may be required to write or revise SOPs, analytical procedures, or other analytical documentation at the discretion of quality control supervisory staff. KEY DUTIES: Perform testing in accordance with written procedures (i.e. USP/EP/JP grade) Documentation of laboratory activities including worksheet/notebook entries according to procedures that define laboratory documentation practices. Processing of electronic data using procedures that ensure data integrity and security. Ship samples to contract testing facilities. Entry of test results from contract laboratories Review and countersign (when necessary) logbooks, notebooks, and worksheets for the purpose of verifying compliance with written procedures, good documentation practices, data integrity and accuracy of calculations. Transcribe results onto analysis reports. Perform daily standardization and performance verifications on laboratory equipment. Comply with site-wide procedures including but not limited to change control, documentation, deviation reporting, cGMP compliance, safety, and electronic data security. Identify deviations to written procedures. Disposal of laboratory waste on an as needed basis. Identify and report unsafe conditions within the laboratory. Identify OOS results, atypical results, and atypical laboratory events requiring a laboratory investigation; perform investigative testing. SKILLS/ABILITIES: Ability to perform routine analysis, such as wet chemistry and operate basic laboratory equipment. Understands paperwork review process. Ability to follow written procedures and exhibit excellent documentation practices. Basic laboratory knowledge and skills analytical techniques in wet chemistry/chromatography Practical experience with various types of laboratory instrumentation Troubleshooting skills with analytical methodology and instrumentation. Technical writing skills Employee must be able to pass a vision exam prior to employment and annually thereafter. PERSONAL ATTRIBUTES: Proactively achieves results for the best of the organization. Willingness to learn new things. Ability to function in a small company atmosphere. Ability to cope with a rapidly changing work environment. Commitment to teamwork. Commitment to continuous improvement in all areas. Ability to focus attention to details and ensure high quality work. Ability to work safely; seek out and encourage safe practices Responsible for managing their time, organizing their workload to be efficient, and have good organizational and communication skills EDUCATION AND EXPERIENCE: Bachelors Degree in Chemistry with 0-2 years of laboratory experience. Other fields of specialty in Sciences are also acceptable provided sufficient chemistry coursework is completed. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Our client, a global CDMO, offering products and services across the drug development spectrum is looking for a skilled QC Analyst III to join their team in Ventura County, CA! Job Title: QC Analyst III Job type: 6 month contract - hire Pay rate: $37 - $39/ hr. Job Summary: We are seeking a highly skilled and detail-oriented Senior QC Analyst to perform complex analytical testing in support of pharmaceutical product development and manufacturing. The ideal candidate will have advanced experience in chromatography techniques (e.g., HPLC, UPLC, GC), method validation, data analysis, and regulatory compliance. This position plays a critical role in ensuring product quality, supporting investigations, and driving continuous improvement across the QC function. Key Responsibilities: Perform complex analytical testing including Liquid Chromatography (HPLC/UPLC), Gas Chromatography (GC), and other instrumental and wet chemistry techniques. Troubleshoot analytical instruments and resolve method or equipment-related issues. Participate in and assist with test method validations, verifications, and transfers. Evaluate and analyze test data to identify trends, outliers, or potential issues. Support OOS (Out of Specification) and OOT (Out of Trend) investigations, including CAPA (Corrective and Preventive Action) documentation. Coordinate testing activities with external laboratories, including raw material and specialized testing. Execute, author, and review SOPs, test methods, protocols, reports, investigations, change controls, and data summaries. Utilize risk assessment and root cause analysis tools (e.g., 5 Whys, Fishbone) to support investigations and process improvements. Manage aspects of the stability program, including scheduling, testing, and reporting, and investigate aberrant stability results. Qualifications: Bachelor's or Master's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific field. 3-6+ years of relevant experience in a regulated laboratory environment (pharmaceutical, biotech, or similar). Strong technical expertise in HPLC, UPLC, GC, and other analytical techniques. Working knowledge of cGMP regulations, ICH guidelines, and regulatory expectations. Experience with method validation and stability programs preferred. Ability to manage multiple tasks and work independently in a fast-paced environment. Experience with electronic data systems (e.g., Empower, LIMS, TrackWise, MasterControl). Note: This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Yoh is hiring a Sr. QA Technician for our Pharmaceutical Manufacturing client in St. Louis, Missouri. This is a great opportunity to expand your skillsets and join a growing team! Job Responsibilities: Ensure completion of require training, work (including document review, batch release, QA on-the-floor, AQLs), and timely release of materials and batches. Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP). Responsible for the thorough and efficient review and disposition of completed batch record documentation ensuring adherence to Good Documentation Practices, cGMPs and applicable local procedures. Responsible for performing and / or overseeing performance of Quality Assurance On The Floor tasks including but not limited to performing AQL inspections, performing clearances for manufacturing areas and providing Quality input and guidance to manufacturing personnel. Responsible for with dispositioning finished product, raw materials/ components and intermediates through an all-inclusive documentation review and cross reference of electronic quality systems. Responsible with release of incoming raw materials and components per applicable local procedures. This may include support for labeling dispositioned raw materials and components with appropriate status indicator labels. Ensure a safe and quality working environment through training, awareness, and compliance to safety/Quality guidelines and SOP's. Ensure the maintenance of department, premises and equipment. Perform all work in compliance with site safety and radiation protection guidelines. Assist with quality investigations in order to determine root cause and applicable CAPAs. Skills/Education Required: Associate Degree in life science or a related field with completion of 4 college-level life science courses required. Bachelor Degree in life science or a related field preferred. Work experience is considered in lieu of degree. Three or more years of quality and production experience in a cGMP environment/facility. Working Conditions: Willing to work in plant producing radioactive materials and complete required safety trainings to work on the floor. The ability to lift up to 70 pounds, kneeling, crouching, twisting the upper body, walking, bending, stooping, pushing, pulling, reaching, must be able to physically negotiate stairs and evacuation ladders with or without accommodation, wear and operate safety equipment, enter vessels, and inspect equipment. Must be willing to wear a variety of Personal Protective Equipment (PPE) and hearing protection as needed. Must be able to work indoors and outdoors with exposure to mechanical/moving parts, hazards including corrosive, flammable and toxic material, dust, dirt, odors, and irritants. Schedule: 8:00 am - 4:30 pm, Monday - Friday Estimated Min Rate: $20.30 Estimated Max Rate: $29.00 What's In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh's network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh's extensive talent community that will provide you with access to Yoh's vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week) Health Savings Account (HSA) (for employees working 20+ hours per week) Life & Disability Insurance (for employees working 20+ hours per week) MetLife Voluntary Benefits Employee Assistance Program (EAP) 401K Retirement Savings Plan Direct Deposit & weekly epayroll Referral Bonus Programs Certification and training opportunities Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day & Zimmermann company, 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, disability, or status as a protected veteran. Visit ************************************************ to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. 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. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh's hiring clients' preferences. To learn more about Yoh's privacy practices, please see our Candidate Privacy Notice: **********************************

Title: Sterility Assurance Scientist Duration: 6 Month Contract (potential of extension) Responsibilities: The Sterility Assurance Scientist is a technical role that assists in development and implementation of the site's sterility assurance programs and provides technical guidance and expertise in environmental monitoring, contamination control, aseptic process simulations, gowning/aseptic techniques, and cleaning/sanitization strategies, including disinfectant efficacy. The principal role is a position that develops and implements a technical agenda and is responsible for providing technical leadership for the Parenteral Process Team. The principal role is also expected to serve as a mentor within the TSMS team and engage in upstream and external to site activities related to sterility assurance contamination control strategies are established. Key Objectives/Deliverables • (Associate/Senior) Ensure and provide oversight and technical guidance for sterility assurance programs at the manufacturing floor level. • Lead or provide technical oversight for Provide technical support for activities related to sterility assurance programs including but not limited to: • Airflow Pattern Testing • Environmental Monitoring Performance Qualifications • Aseptic Process Simulations • Cleaning, Sanitization, and Disinfection • Gowning within GMP Classified Areas • Aseptic Processing Techniques • Contamination Control • Assist in the development and implementation of processes and facility monitoring to ensure effective contamination control strategies are established. • (Senior) Lead or assist in the development and implementation of processes and facility monitoring to ensure effective contamination control strategies are established. • (Senior) Lead/assist with support and/or provide technical expertise for developing the site's contamination control strategy and cleaning and sanitization program/strategy, and disinfectant efficacy strategies. • (Senior) Lead/assist with support and/or provide technical expertise for the facility's cleanroom gowning and aseptic technique strategy/program. • (Principal) Knowledge in pharmaceutical Microbiology, related to microbiological media, microbiological enumeration techniques, and microorganism isolation and identification. • (Principal) Lead/provide technical oversight for one or both the Environmental Monitoring (EM) or Aseptic Process Simulation (APS) program: • (EM) Authoring EM Performance Qualifications (EM PQ) and overseeing the execution. • (EM) Evaluating EM data and authoring EM Trend Reports. • (EM) Assist with identifying facility environmental isolates and how to create and maintain environmental isolated cultures. • (APS) Authoring APS protocols and overseeing the execution. • (APS) Evaluating the APS data, including personnel qualifications, and authoring APS reports. • (APS) Assist with tracking and tending APS to ensure all regulatory requirements and Global Quality Standards are met for each manufacturing line/process. • Apply sterility assurance risk management to evaluate manufacturing processes and associated controls with respect to potential introduction of microbial, endotoxin, and particulate contamination. • Analyze microbial and manufacturing data to identify trends, process discrepancies, and opportunities for continuous improvements.• Lead or provide technical support for root cause investigations associated with sterility assurance programs. • Participate and/or provide technical sterility assurance support during internal and external audits. • Create, execute, review, and/or approve technical documents and change controls related to sterility assurance programs. • Work within cross-functional teams to implement TS/MS objective and deliver on business and quality objectives. Basic Qualifications: • Bachelor's or master's degree in microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical Engineering, or other related scientific discipline. • Demonstrated understanding and relevant experience of scientific principles required for manufacturing parenteral drug products within operations, microbiology, environmental monitoring, sterility assurance, validation, technical services, and/or quality assurance associated cGMP pharmaceutical manufacturing. • (Senior) 2+ years in pharmaceutical manufacturing (Microbiology, TSMS, Sterility Assurance, or related dept). • (Principal) 5+ years in pharmaceutical manufacturing (Microbiology, TSMS, Sterility Assurance, or related dept). Additional Skills/Preferences: • Possess strong interpersonal skills to work cross-functionally within a team. • Possess strong self-management and organizational skills. • Possess strong oral and written communication skills for communicating to colleagues, management, and other departments. • Experience with data analysis and trending. • Ability to wear appropriate PPE and other safety related equipment or considerations in manufacturing warehouse, or laboratory areas. • Ability to gown into facility dedicated cleanroom attire, as required to perform job responsibilities. Additional Information: • Role is Monday through Friday based and will be phased from a project support role to a routine support role as the development facility and processes progress. Must be flexible in providing support to accommodate other inputs (production schedules, shutdowns, etc.). Occasional extended hours and / or off-hour work may be required. • Tasks may require repetitive motion and standing or walking for long periods of time. • Travel may be required during the project phase for training and implementation of sterility assurance programs. This is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the . For GMP purposes, the job description should be updated for significant changes. As always, you should consult with your supervisor regarding your actual job responsibilities and any related duties that may be required for the position.

Quality Control Inspector Needed in Camarillo Direct Hire Industry: BioTech, Pharmaceuticals Pay range: $23 - $24/hour Monday - Friday 7am - 3:30pm Must Have * Understanding of global pharmaceutical product regulations with experience with ISO 9001 and/or 13485:2003 and 21 CFR Parts 210 and 211 and/or Part 820. * Demonstrated ability to perform GMP operations following detailed SOPs, maintaining training, and good documentation practices. * Minimum of 2 years' experience with technical documentation for quality activities. This experience should be in the areas of the Quality manufacturing that includes quality inspections and corrective actions in a pharmaceutical or medical device environment. Job Summary Performs quality control inspections in all aspects of operations, checks, and test during the manufacture of products. Inspect incoming materials, and products at different stages of production. Records observations and make recommendations for improving processes. Essential Functions * Responsible for all activities involving quality inspections and compliance with applicable regulatory requirements; * Conduct inspection and testing related to: ► Incoming product. ► First article. ► In-process. ► Final. * Initiate nonconformance reports (NCR). * Performs all aspects of testing related to manufacturing. o Incoming inspections o In-process inspection. o Final Inspection release of finished goods. o Document review. o Supports cross functional departments investigate potential non-conformance's observed * Ensures that all inspections and procedures are properly completed and documented. * Perform pre and post-inspection of product gamma irradiation process. * Approve or reject raw materials with respect to quality standards and communicate results to all pertinent parties. * Initiate nonconformance reports (NCR) for all non-conforming material identified throughout operations * Prepare and submit Metrics reports to the quality supervisor or QC lead * Comply with all safety requirements ensuring work areas meet standards. * May be required to report to multiple facilities within a 2-mile radius. * Job Order document review and release * Other duties as assigned Education * High School Diploma or equivalent with 2 years of experience in quality control inspections. Required Experience & Competencies * Understanding of global pharmaceutical product regulations with experience with ISO 9001 and/or 13485:2003 and 21 CFR Parts 210 and 211 and/or Part 820. * Demonstrated ability to perform GMP operations following detailed SOPs, maintaining training, and good documentation practices. * Minimum of 2 years' experience with technical documentation for quality activities. This experience should be in the areas of the Quality manufacturing that includes quality inspections and corrective actions in a pharmaceutical or medical device environment. * Solid organizational and planning skills required. * Ability to communicate effectively, verbally and in writing, demonstrate good interpersonal skills interdepartmentally and with external vendors and contractors. * Must be able to work effectively and efficiently in a team environment. * Must have the following personal attributes: integrity and trust, work ethic, sound judgment, intellectual honesty, pragmatism, courage and conviction. * Must display personal accountability for results and integrity. * Must display eagerness to learn and continuously improve. * Must have uncompromising dedication to quality. * Good general mathematical skills. * General knowledge and use of measuring devices such as calipers, tape measures, rulers, pin gauges * General computer skills. All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

Job Titles: Quality Inspector Shift time: Monday - Thursday - 2nd shift - 3:30pm - 2am Performs new and routine inspections, checks, tests and sampling procedures of standard parts. Responsible for receiving, in-process, or final inspections as required. Duties and Responsibilities Responsible for utilizing aptitude in measurement techniques, metrology, and blueprint reading and verify operators are accurately measuring and recording dimensions on IP sheets or other documentation. Perform first article and first piece approval for operators. Perform inspection duties for in-process and final inspection. Complete and review non-conformance documentation. Support quality improvement and cost savings initiatives, as required. Assist Quality Engineers, as required. Assist in other production areas, as needed. Perform other quality or document control duties, as assigned. Perform part measurement on CMM.

Our client is hiring CWI QA/QC Inspectors and Supervisors in Reno/Sparks, NV area. These are Direct Hire positions offering a Full Benefits package and relocation assistance. Essential Duties & Responsibilities: Plans and conducts the analysis, inspection, design, test, and/or integration to assure the quality of assigned product or component. Performs quality engineering reviews of design documentation for compliance with stated requirements, including vendor quality manuals and company quality records. Reviews all purchased products or components and provides input to the decision of whether to accept the product and future purchases from the vendor. Documents data obtained during all quality assurance activities, consistent with company policies and procedures. Communicates significant issues or developments identified during quality assurance activities and provides recommended process improvements to management. Prepares reports to communicate involvement and results of quality assurance activities. Other duties as assigned. Qualifications: Seeking at least 2 years of experience in Quality Control focused on ASME B31 piping codes, industrial and commercial construction, fabrication, welding, non-destructive testing, and/or other similar fields. Current certification in accordance with AWS QC-1 as a Certified Welding Inspector (CWI) preferred. Excellent time management and written and spoken communication skills, highly professional, organized, and trustworthy team player. Must be able to pass a background check and a drug test.

Pride Health is hiring a Quality Control Technician to support our client's medical facility based in Elmhurst, Illinois. This is a 13-week contract job opportunity and a great way to start working with a top-tier healthcare organization! Job Summary: The Sterile Processing Quality Control Technician ensures the highest standards of instrument cleanliness, assembly accuracy, and quality assurance in sterile processing operations. This role combines hands-on technical processing responsibilities with detailed inspection and documentation tasks critical to patient safety and process reliability. This position focuses on quality assurance beyond standard sterile processing technician duties, ensuring compliance with all regulatory and internal standards while maintaining an unwavering commitment to safety and process excellence. Job Responsibilities: -Follow all ANSI/AAMI standards, manufacturer Instructions for Use (IFUs), SOPs, and company Work Instructions. -Decontaminate used surgical instruments and equipment using proper PPE and protocols. -Disassemble, clean, and reassemble complex surgical instruments as required. -Accurately assemble and package instrument trays and sets per guidelines. -Operate washers, sterilizers, and other processing equipment safely and effectively. -Inspect instruments for cleanliness, functionality, and damage prior to packaging. -Document missing or damaged instruments per SOPs. Required Skills & Experience: -Hands-on experience in sterile processing, demonstrating proficiency in decontamination, assembly, and sterilization procedures. -Strong attention to detail. -Ability to work effectively under pressure in a fast-paced, team-oriented environment. -General knowledge of surgical instruments and processing protocols. -Knowledge of sterilization techniques, including steam sterilization and infection control practices. -Familiarity with ANSI/AAMI standards and manufacturer Instructions for Use (IFUs). Additional Information: Location: Elmhurst, Illinois Schedule: 2nd Shift- 3 pm-11:30 pm & 3rd Shift- 11:00 pm-7:30am Pay Range: $24/Hr. - $28/Hr. Start: 12/15/2025 *Offered pay rate will be based on education, experience, and healthcare credentials. Interested? Apply now! About Pride Health As a certified minority-owned business, Pride Global and its affiliates - including Russell Tobin, Pride Health, and Pride Now - are committed to creating a diverse environment and are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, pregnancy, disability, age, veteran status, or other characteristics. Pride Global offers eligible employee's comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance, and hospital indemnity), 401(k)-retirement savings, life & disability insurance, an employee assistance program, legal support, auto, home insurance, pet insurance, and employee discounts with preferred vendors.

We have a great opportunity for an experienced Quality Inspector- GD&T Specialist Full time, 1st shift position. Pay: $20-$28/hour Responsibilities: Perform final inspections of finished products for quality and compliance to specifications Interpret and apply Geometric Dimensioning and Tolerancing (GD&T) to verify product dimensions Confirm compliance with special processes, material specifications, and Non-Destructive Testing (NDT) certifications Conduct visual inspections for surface finish, coatings, and part markings Use precision measuring tools such as micrometers, calipers, and height gauges Document inspection results and report non-conformances to the production team Collaborate on continuous improvement initiatives to enhance quality and efficiency Qualifications/Experience: High school diploma or equivalent Minimum of 2 years of quality inspection experience in a manufacturing environment Strong working knowledge of GD&T and ability to read and interpret engineering drawings Familiarity with materials, special processes, and NDT certifications Experience using precision measuring tools Proficient with Microsoft Office; experience with quality management systems is a plus Ability to lift up to 50 lbs and work both independently and as part of a team Compensation: Competitive wages based on experience Healthcare coverage, including vision and dental 401(k) with company contribution and profit sharing Paid time off and paid holidays Performance-based bonuses If qualified and interested in this position, contact Recruiter Damaris Diaz, call 203-213-6925 or email, damaris.diaz@expresspros.com

Ultimate Staffing's client is seeking a Quality Control Inspector to ensure the highest standards of quality and operational efficiency within their warehouse environment. This role is critical in maintaining compliance, accuracy, and safety across all warehouse processes. Position Overview The Quality Control Inspector is responsible for developing and implementing quality control processes, inspecting products prior to shipment, and ensuring adherence to company policies and safety standards. This position plays a key role in validating inventory accuracy, supervising warehouse operations, and leveraging systems such as CargoWise for robust tracking and validation. Key Responsibilities Quality Assurance & Compliance Inspect products before they leave the warehouse to ensure accuracy and quality. Verify barcodes, labels, and documentation for all outgoing shipments. Ensure compliance with company policies, OSHA regulations, and industry standards. Oversee damage control procedures for defective or damaged goods. Warehouse Operations Direct and monitor daily activities including receiving, scanning, storing, picking, packing, and shipping. Optimize warehouse layout and processes for maximum efficiency. Ensure orders are fulfilled accurately and on schedule. Team Leadership Supervise, train, and support warehouse staff to maintain high performance. Assign tasks, evaluate employee performance, and promote a safe, collaborative work environment. Inventory Management Maintain inventory accuracy through cycle counts and reconciliation. Investigate and resolve discrepancies in coordination with office and warehouse teams. Process Improvement & Reporting Identify operational bottlenecks and recommend workflow improvements. Assist in implementing new technologies or procedures to enhance productivity. Prepare daily/weekly reports on warehouse performance, inventory, and staffing needs. Qualifications High school diploma or equivalent (Associate or Bachelor's degree preferred). 5+ years of warehouse experience, including supervisory experience. Strong understanding of inventory systems, warehouse procedures, and logistics operations. Proficiency with WMS and computer applications (MS Office, Excel; CargoWise experience preferred). Ability to lift and move heavy materials as needed. Key Competencies Leadership & team management Attention to detail and safety awareness Organizational and time management skills Problem-solving and adaptability Requirements Minimum 5 years of management experience in a warehouse/distribution environment. Expertise in quality control, logistics, and inventory management. Working knowledge of OSHA, HAZMAT, and FDA regulations (certifications preferred). Excellent supervisory, customer service, analytical, and mathematical skills. Hands-on approach and willingness to assist where needed. Desired Skills and Experience Ultimate Staffing's client is seeking a Quality Control Inspector to ensure the highest standards of quality and operational efficiency within their warehouse environment. This role is critical in maintaining compliance, accuracy, and safety across all warehouse processes. Position Overview The Quality Control Inspector is responsible for developing and implementing quality control processes, inspecting products prior to shipment, and ensuring adherence to company policies and safety standards. This position plays a key role in validating inventory accuracy, supervising warehouse operations, and leveraging systems such as CargoWise for robust tracking and validation. Key Responsibilities Quality Assurance & Compliance Inspect products before they leave the warehouse to ensure accuracy and quality. Verify barcodes, labels, and documentation for all outgoing shipments. Ensure compliance with company policies, OSHA regulations, and industry standards. Oversee damage control procedures for defective or damaged goods. Warehouse Operations Direct and monitor daily activities including receiving, scanning, storing, picking, packing, and shipping. Optimize warehouse layout and processes for maximum efficiency. Ensure orders are fulfilled accurately and on schedule. Team Leadership Supervise, train, and support warehouse staff to maintain high performance. Assign tasks, evaluate employee performance, and promote a safe, collaborative work environment. Inventory Management Maintain inventory accuracy through cycle counts and reconciliation. Investigate and resolve discrepancies in coordination with office and warehouse teams. Safety & Equipment Conduct safety inspections and enforce proper use of equipment (forklifts, pallet jacks, scanners). Report incidents and implement corrective actions to maintain a hazard-free workplace. Process Improvement & Reporting Identify operational bottlenecks and recommend workflow improvements. Assist in implementing new technologies or procedures to enhance productivity. Prepare daily/weekly reports on warehouse performance, inventory, and staffing needs. Qualifications High school diploma or equivalent (Associate or Bachelor's degree preferred). 10+ years of warehouse experience, including 5+ years in a supervisory role. Strong understanding of inventory systems, warehouse procedures, and logistics operations. Proficiency with WMS and computer applications (MS Office, Excel; CargoWise experience preferred). Ability to lift and move heavy materials as needed. Key Competencies Leadership & team management Attention to detail and safety awareness Organizational and time management skills Problem-solving and adaptability Requirements Minimum 5 years of management experience in a warehouse/distribution environment. Expertise in quality control, logistics, and inventory management. Working knowledge of OSHA, HAZMAT, and FDA regulations (certifications preferred). Excellent supervisory, customer service, analytical, and mathematical skills. Hands-on approach and willingness to assist where needed. All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

Our client, a well-established manufacturer serving regulated industries, is growing and seeking a Quality Inspector to join their 3rd shift. This position is ideal for someone who enjoys hands-on work and takes pride in maintaining high standards of quality. Product Quality Inspector - 3rd Shift (11PM-7AM) Training: 1st Shift (7AM - 3PM) for the first 3-6 months Responsibilities: · Perform hands-on product testing and inspections to ensure compliance with specifications · Accurately update and maintain product testing databases and quality documentation · Record data in both manual and electronic files · Communicate any non-conformance issues promptly to production teams and supervisors · Assist with documentation control and manage retain samples and related records Requirements: · Previous hands-on experience in Quality Inspection or a similar role · Strong attention to detail, organized, and results-oriented · Ability to work independently and collaboratively · Basic math skills and computer literacy required · Must be able to train on 1st shift for 3-6 months then transitioning to 3rd shift · Familiarity with ISO 9001 or other international quality standards is advantageous Why You'll Love It Here: This family-owned company offers a union environment, a culture focused on employee development, and real opportunities for career growth. If you're detail-driven, adaptable, and ready to grow, this is the role for you! Benefit offerings for full-time employment include 10 paid Holidays, and 10 PTO days, prorated based on hire date within the calendar year. Also included: Medical, dental, vision, term life and AD&D insurance, long-term disability, employee assistance program, onsite gym, and a 401k plan. Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to ******************************************* The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: • The California Fair Chance Act • Los Angeles City Fair Chance Ordinance • Los Angeles County Fair Chance Ordinance for Employers • San Francisco Fair Chance Ordinance

Location: Rochester MA (100% On-site), 1st shift only 6:30A-3:30P M-F, salary range $72K-$82K, full-time role: health insurance with an HRA, dental, vision, LTD, and a 401(k) retirement plan with an employer match. 3 weeks PTO, 1 week sick. Generous relocation package offered. Qualified candidates are encouraged to apply. Large precast concrete supplier in Massachusetts and New Hampshire, providing high-quality products for over 70 years. Their extensive product range includes septic tanks, manholes, drainage structures, bulkheads, curbing, residential steps, and retaining wall systems, all crafted to precise specifications. They cater to engineers, contractors, and homeowners, emphasizing superior performance and exceptional customer service. The Quality Control Technician (“QC Technician”) will work within the production plant and is ultimately responsible for product testing. The QC Tech will assist in the execution of quality control processes, procedures and protocol associated with the production of pre and post concrete pours. Responsibility Responsible for ACI concrete field tests Responsible for quality control inspections in manufacturing plant Inspect forms before pouring (Pre-Pour). Inspect product after removed from forms (Post-Pour) Notifies Production Supervisor if deficiencies are found. Perform and/or schedule repairs on products as needed. Housekeeping - maintain a clean work area. Including cleanliness within breakroom, restroom, and general facility areas. Expected to maintain knowledge of precast plant techniques and procedures. May assist with precast production operation as needed. Characteristics Always committed to safety. Maintain a safe work area. Follow safe work practices as outlined in the Safety Program. Always committed to quality. Follow and implement quality control measures. Excellent attendance. Reliable means of transportation to and from work. Ability to learn, organize and prioritize work and handle multiple tasks. Outstanding attitude, honesty, and ethic at all times. Expected to use sound judgment, diplomacy, and discretion. Work independently or cooperatively with others. Self-drive in carrying out the functions of the job. Requirements: ACI Concrete Field-Testing Grade 1 Certified (preferred) NPCA PQS Training Must be at least 18 years of age per federal guidelines. Good communication skills, both verbal and written to all levels of staff Ability to remain focused in busy environment. Computers and tablets skills in order to perform tasks. Ability to read blueprints and sketches.

Staffworks Group is hiring Full Time "Quality Workers" in Greer, SC 3rd Shift: 7:00 pm am-6:10 am, Monday through Saturday $16.00/hour Staffworks Group is an Equal Opportunity Employer Job Perks for Quality Inspectors: Climate Controlled Free/Safe Parking Weekly Pay/Benefits Entry Level Long Term Assignment As an assembly worker, you will: Documents inspection results by completing reports and logs; summarizing re-work and waste; and inputting data into a quality database. Knowledge of the manufacturing environment is a plus Maintains a safe and healthy work environment by following standards and procedures and complying with legal regulations. Problem-solving and people skills. High accuracy in work and attention to detail. Approve incoming materials by confirming specifications; conducting visual and measurement tests; and rejecting and returning unacceptable materials This is a full-time, long-term opportunity. The ideal quality worker: 18 years of age or older High school diploma or GED Follow written and verbal instructions Hand/Eye coordination Fine motor skills for repetitive tasks Ability to stand for long periods of time Able to use power tools Must wear steel-toe shoes Staffworks Group is an Equal Opportunity Employer#talroogreer

We are searching for a Quality Assurance Technologist in the Arnold, PA area Responsibilities: Monitor quality in your area - grading products and documenting results to oversee sanitation. temperatures, GMP's and more. Conduct routine inspections Identify and act on out-of-spec products Interpret safety documentation updates, and perform pre-op sanitation checks - following up to guarantee proper cleaning and sampling procedures. Requirements: Food industry experience preferred High School diploma or GED required Details: SECOND SHIFT - Must be able to train on 1st and be available to work weekends. $25/hr. Click on apply now for instant consideration for this position. Pay Details: $25.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for Employers San Francisco Fair Chance Ordinance Massachusetts Candidates Only: 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.

A manufacturing company in Norwalk, CT is looking for a Quality Control Operator. The ideal candidate will have a keen eye for detail, strong analytical skills, and a commitment to continuous improvement. Primary responsibilities will involve monitoring the production process, conducting routine inspections, and performing tests on materials and finished products. You will work closely with production teams to identify and rectify any quality issues, ensuring compliance with industry regulations and internal standards. The Quality Control Operator will also be responsible for maintaining accurate records of inspections and tests, providing feedback to team members, and assisting in the development of quality control procedures. Responsibilities Conduct routine inspections of products during various manufacturing stages. Perform tests on raw materials and finished products to ensure compliance with quality standards. Document inspection results and communicate findings to relevant team members. Identify and report any quality issues or deviations from established standards. Collaborate with production teams to implement corrective actions and improve processes. Assist in the development and maintenance of quality control procedures and protocols. Participate in internal audits and assist with external audits as needed. Requirements High school diploma or equivalent; additional certifications in quality control preferred. Proven experience in a quality control role, preferably in a manufacturing environment. Strong attention to detail and excellent analytical skills. Ability to interpret technical documents, blueprints, and quality standards. Strong communication skills, both written and verbal, with the ability to work effectively in a team. Pay is $22/hr Hours are Monday - Friday 7:50am - 4:20pm. Must be able to pass background check.

Employment Type: Intern Division: Field Operations Department: Quality Salary Range: $23 - $28/hour The Quality Intern supports the Quality department in implementing and monitoring quality management processes across multiple projects in various phases of construction. This role offers broad exposure to construction operations while working closely with Quality Program Managers to uphold and enhance project standards. Responsibilities / Essential Functions * Participate in the quality program by attending meetings, performing inspections, and verifying materials. * Assist with coordination and content development for Quality pre-operational meetings. * Provide technical support on project sites, including interpreting contract drawings and submittals. * Develop an understanding of project schedules and critical path activities. * Collaborate with Quality Program Managers on initiatives such as drain assembly analysis, finish floor build-up analysis, and water intrusion control planning. * Perform other tasks as assigned by the team. Key Skills * Excellent written and verbal communication skills. * Strong initiative and problem-solving abilities. * High attention to detail. * Effective time management with the ability to handle multiple responsibilities and meet deadlines. * Ability to work in a team environment with a primary focus on collaboration. Required Experience * Pursuing a Bachelor's Degree in Construction Management, Engineering, or a related field (preferred). * Demonstrated interest in construction management and the construction industry.