Quality technician jobs in Worcester, MA - 769 jobs

100% ONSITE WORCESTER MA Pay: $29-$32/hr based on shift Required: Recent Graduate with a BS in Biotechnology, Biology, Biological Engineering, Bioengineering, or other relevant science degree. Familiarity with GMP Drug production, following SOPs, Aseptic techniques Job Description: As a Manufacturing Technician, you'll collaborate with our talented engineers, quality experts, and cross-functional teams to execute crucial functions that drive our operations. You'll have the opportunity to leverage state-of-the-art programs such as LIMS, SAP, automated control systems, DCS, PLC, PI, and more. One of the unique advantages of joining this team is our comprehensive 6-week onboarding training program exclusively designed for our manufacturing technicians. You'll receive the support and resources needed to excel in your role right from the start. As a key member of our team, you'll take on a diverse range of responsibilities that encompass Upstream, Downstream, and Core Support functions. Your key responsibilities may include: Following precise verbal and written procedures in a controlled cGMP environment while prioritizing safety regulations. Meticulously documenting processes in corresponding batch records and log sheets, adhering to cGMP and established Standard Operating Procedures. Collaborating with our team to determine innovative process methods and procedures, actively contributing to the continuous improvement of our operations. Demonstrating a strong commitment to safety by diligently wearing personal protective equipment, such as gowning, safety glasses, gloves, and safety shoes. Proactively completing and maintaining training requirements to stay up to date with the latest industry standards. Occasionally going above and beyond by working overtime to meet project deadlines and deliver exceptional results. Managing inventory levels and actively participating in the shipping of finished materials. Conducting sampling and performing in-process analytical testing to guarantee product quality and integrity. Skillfully preparing equipment for operation, including cleaning and sterilization processes (CIP/SIP). Performing pH and conductivity measurements, crucial parameters for process control and optimization. Operating manufacturing equipment, such as glass washers and autoclaves. Contributing to the preparation of buffers and media, vital components of our production activities. Engaging in cell culture activities, ranging from vial thaw to production scale. Responsible for performing key column operations, Tangential Flow Filtration (TFF), and load line setup. Requirements: Bachelor's Degree in a science discipline is highly preferred with 1 year + manufacturing experience. Knowledge of cGMP operations is preferable. The ability to exercise considerable judgment and initiative, as you'll be working on assignments that require critical decision-making. A deep understanding of the implications of your work and the capacity to make well-informed recommendations for effective solutions. The capability to determine appropriate methods and procedures when faced with new assignments, showcasing your adaptability and problem-solving skills. Strong written and verbal skills, enabling effective communication. The ability to read written instructions and/or numbers at close and far ranges. Comfortable working with a computer or tablet for 50-60% of scheduled work time. The ability to thrive in a manufacturing environment with a constant sound level of 75 decibels, which is comparable to the sound of a washing machine. Occasional use of hearing protection may be required to ensure your well-being. Adaptability to spending 50% of your scheduled work time in a stationary position, where your focus and attention to detail will be paramount. Frequently move and position yourself to observe equipment readings, ensuring accurate monitoring and data collection. Work with your team to transport/move equipment weighing up to 50 lbs., with support from appropriate safety equipment. Your safety is our top priority.

Schedule: Mon-Fri (4 days in office required, 1 day optional remote) Compensation: Competitive Salary + Benefits We are a fast-growing AI language technology company seeking a US/LATAM Spanish Linguistic Quality Lead (LQL) to join our AI-focused language team on a mission to build the next generation of operational models. This is a unique opportunity for someone passionate about languages and technology, with the drive to shape the future of AI-powered communication in medical and life sciences translation. What You'll Do Lead linguistic quality assurance for US/LATAM Spanish, with a strong focus on medical device manuals, pharmaceutical content, and other regulated life sciences materials. Train large language models (LLMs) with Spanish linguistic data to enhance AI-driven translation, QA, and automation workflows. Translate, review, and edit Spanish content in active projects, ensuring accuracy, clarity, and regulatory compliance. Recruit, onboard, and manage Spanish linguistic resources (translators, editors, interpreters, interviewers) within our global network. Support project execution, ensuring linguistic excellence and cultural relevance across deliverables. Collaborate with other LQLs to drive workflow improvements and innovation, helping design future operational models. Partner with cross-functional teams at the intersection of language, life sciences, and AI. What We're Looking For Native proficiency in US/LATAM Spanish, with strong command of English. Ideal for your graduates with Spanish linguistic background. Familiarity with CAT tools (e.g., Phrase, Trados, MemoQ, XTM) is a plus but not required. Forward-thinking, creative, and energetic, with a willingness to take on challenges and think outside the box. Diligent, dependable, and committed to quality and continuous improvement. Strong organizational, communication, and problem-solving skills. Ability to work collaboratively with other LQLs, engineers, and project teams in a fast-paced, innovative environment. Work authorization in the U.S. is required. What We Offer Full-time role: Monday-Friday, with 4 days in-office and 1 day optional remote. Competitive salary + paid holidays, sick/personal days, and professional development opportunities. A modern office in Boston's Financial District. The chance to contribute to an AI-driven language team pioneering future business and operational models. A dynamic, entrepreneurial environment where your ideas and contributions have direct impact. This is an exciting role for someone passionate about Spanish language and culture, eager to explore AI-powered translation and linguistic innovation, and motivated to grow with a company shaping the future of language operations in medical and life sciences. How to Apply: Please send your CV to **********************

The Equipment Qualification Technician is responsible for verifying, qualifying, and maintaining the quality and performance of manufacturing equipment (not finished products). This role focuses on ensuring machines and production systems operate reliably, meet qualification standards, and comply with regulatory requirements in a manufacturing environment. Key Responsibilities: Perform IQ, OQ, and PQ on manufacturing equipment Verify machine performance, functionality, and compliance (not product inspection) Document qualification results, deviations, and corrective actions Work hands-on on the manufacturing floor / shop environment Support equipment setup, troubleshooting, and issue resolution Work around production lines, machines, and industrial systems Partner with Engineering, Quality, and Operations teams Participate in root cause analysis, audits, and process improvement activities Train operators and provide technical support once equipment is qualified Experience Prior experience in a manufacturing environment (required) Experience working with machines, equipment, or production lines Experience in regulated environments (GMP / ISO preferred) Technical Skills Equipment qualification or validation exposure (IQ/OQ/PQ preferred) Mechanical aptitude with hands-on troubleshooting and equipment setup Ability to follow and document technical procedures

Industry: Pharmaceuticals Title: Associate, Quality Operations QA Duration: 09 months contract (+Possibility of extension) Onsite with 1x per week flexibility as needed. About the Role The QA Associate will help ensure that life-changing biopharmaceutical products are manufactured to the highest standards. The QA Associate will provide day-to-day QA support across manufacturing, validation, materials, QC, engineering and facility operations at our Norton site, partnering with cross-functional teams to maintain GMP compliance and inspection readiness. Key Responsibilities Provide raw material support, including review/approval of incoming material documentation and release for GMP use. Deliver on-the-floor QA support to manufacturing, including area clearance and changeover operations, ensuring readiness for production activities. Review and approve SOPs, master batch records (MBRs), specifications, risk assessments, and quality documents. Generate and maintain Quality-related SOPs and controlled forms. Review and approve validation documents and protocol executions to confirm compliance with approved procedures and regulatory requirements. Review and approve QC laboratory qualification documents, including equipment qualification. Perform executed batch record review and approval to ensure accuracy and compliance. Review and approve deviations, CAPAs, Change Controls and related investigations in the quality management system. Support partner audits and regulatory inspections, including document retrieval and subject matter input. Approve work orders in the maintenance system to verify equipment maintenance and calibration compliance. Collaborate with internal cross-functional teams at the Norton facility to drive continuous improvement and quality excellence. Qualification/Skills Bachelor's degree in a scientific or engineering discipline (Biology, Chemistry, Biotechnology, etc.) or equivalent experience. 2-4 years of GMP experience in Quality, Manufacturing, or QC. Knowledge of cGMP regulations (21 CFR Parts 210/211/11, ICH Q7/Q10) and Good Documentation Practices. Strong attention to detail, organizational skills, and the ability to communicate effectively across teams. Experience with quality systems (e.g., Veeva, SAP) is a plus.

Vaxess is developing a pipeline of next-generation therapeutics on our novel micro-array patch platform. With only five minutes of wear-time on the skin, the Vaxess' patch combines room temperature stability with simplified application to dramatically alter the way that drugs are delivered. Vaxess is committed to enabling products that are not only more effective, but also more accessible to patients around the world. Responsibilities Perform cGMP manufacturing operations according to documented procedures or batch records Operate automated manufacturing equipment and record relevant in-process data. Complete production and testing records following Good Documentation Practices (GDP) Handle, assemble, and visually inspect products, including use of a microscope, automated inspection systems, or other optical systems. Contribute to root cause analysis (RCA) and help contribute to manufacturing investigations Support manufacturing related R&D efforts as needed Perform other assigned duties related to manufacturing, quality control, and/or facility operations. Qualifications 2 + years' relevant experience working in regulated environments in medical device or biopharmaceutical industries; experience working in a clean room is preferred High school diploma minimal, associate's degree or trade certifications preferred Good written and verbal communication skills, attention to detail, and a demonstrated ability to work effectively within a team Ability to stand or sit for a full shift on a manufacturing line Entrepreneurial spirit and drive to positively impact global human health At Vaxess, we're bringing together exceptional talent to drive our product development forward. We value collaboration, curiosity, and a dynamic work environment. To apply, please submit your CV/resume to ****************** .

Pay Range $41-$43 per hour hybrid role (3 days onsite/week) Work Schedule: Dayshift This position will, under BPO supervision, execute deliverables for a project to implement new, fully Electronic Lab Notebook (ELN) system. This is a non-laboratory testing position. This position will be responsible for performing activities towards the design, configuration, and validation of the new ELN system, recreation and/or migration of required master data, and involvement in deployment of production instances at the site(s). This position will be expected to adhere to established procedures (Standard Operating Procedure, Work Instruction) for safety and cGMP/CFR requirements which includes, but is not limited to, expectations of training and documentation practices. This position will work in a team environment, collaborating with various colleagues in the network to ensure project commitments are met. They will report status/updates of key responsibilities and escalate any issues through the project management team. Key Responsibilities for the new ELN system: Participate in process engineering activities Facilitate the development of new business SOPs, Forms, Manuals, etc. using new processes/workflows Participate in system requirement, software configuration, and design activities Receive and/or verify master data for the site(s) Coordinate ELN Template development and review with site SMEs Support the development and review of Operational Qualifications Execute User Acceptance Testing & Data Migration Verification Review and provide input on training materials Support training material development by providing inputs and reviews Support site Instrument Qualification activities such as planning and execution Basic Qualifications Bachelor's degree and 2 years of industry Quality Control or Quality experience OR Associate's degree and 6 years of industry Quality Control or Quality experience OR High school diploma / GED and 8 years of industry Quality Control or Quality experience Preferred Qualifications (Top 3 first, listed in order) GxP experience, specifically practices and requirements in the testing of biopharmaceuticals. Experience and knowledge in using electronic lab notebook systems (Biovia OneLab, ThermoFisher Sample Manager, LabWare, Benchling, etc.). Advanced proficiency in Microsoft Office (i.e., Outlook, Word, Excel, PowerPoint). Experience in the use of other industry systems such as Veeva & Empower. Experience in testing or with processes involving analytical methods. Excellent problem-solving capabilities and attention to detail. Experience of collaboration within and across functional areas. Excellent written and verbal communication skills. Experience in development and validation testing of software used in a GMP environment.

Quality Inspector III - Weekdays About Us Founded in 2015 to develop the world's first industrially scalable laser metal additive manufacturing solution, our client is reshaping how the world manufactures critical products. They build and operate advanced digital infrastructure that enables innovation, accelerates growth, and supports sustainability across aerospace, defense, medical, and other essential industries. Through vertically integrated capabilities, including scalable additive manufacturing and precision machining, they deliver true end-to-end production at scale by combining cutting-edge technology with a foundation of proven industrial craftsmanship. Their team brings deep expertise in manufacturing, materials science, software, automation, and operations, united by a shared commitment to quality, curiosity, and accountability. They foster an inclusive culture where people take ownership, solve meaningful problems, and continuously learn, because diverse perspectives lead to better outcomes. Job Purpose As a Quality Inspector III at our client, you will work in a diversified role within the Quality Inspection team dedicated to ensuring every product delivered meets the highest standards of precision, safety, and reliability. By applying expertise in inspection methods, quality systems, and problem-solving, this role safeguards customer trust, drives continuous improvement, and supports innovation in metal additive manufacturing. This position operates on the weekday shift: Monday-Friday, 6:00 AM to 2:30 PM. Key Responsibilities Perform First Article Inspections (FAI) and routine part inspections using calipers, micrometers, and other gauges. Verify that materials, equipment, processes, and products comply with quality specifications. Develop and validate inspection and test methods; assist in creating SOPs and inspection protocols. Monitor, analyze, and report on product quality metrics. Support compliance with customer, internal, and industry requirements (AS9100, ISO 9001, ISO 13485) through audits and gap analysis. Assist in developing and implementing process controls, corrective actions, and continuous improvement initiatives. Ensure workflows, processes, and products comply with safety regulations. Investigate and troubleshoot product or production issues. Inspect manufactured parts, issue non-conformance reports, and facilitate MRB hardware disposition and corrective action tasks. Work independently and manage daily priorities with minimal supervision. Communicate and collaborate with operations personnel to ensure production needs are met. Initiate and communicate identified nonconformances. Qualifications 5+ years of experience performing part inspections with strong drawing interpretation skills. Extensive knowledge of GD&T principles. Experience with First Article Inspections (FAI), Test Method Validation (TMV), and developing inspection methods. Proficiency in AQL sampling techniques. Skilled in performing dimensional and visual inspections. Experience with root cause analysis, data analysis, and troubleshooting. Experience in medical device, aerospace, or defense manufacturing required. Hands-on experience with advanced inspection equipment and software, including CMMs, PCMMs, vision systems, profilometers, and blue-light scanners (e.g., Zeiss, Faro, Keyence). Ability to troubleshoot issues encountered with inspection equipment. Self-motivated, hands-on team player with excellent communication skills; adaptable to fast-paced environments and excited by new challenges in metal additive manufacturing.

Engineering Technician - Medical Device R&D temp to perm Marlboro, MA Support engineers in the development and testing of single-use medical devices. This hands-on role involves working with Engineers testing prototypes, performing validation and system testing, and accurately documenting results in a regulated environment. Responsibilities Perform validation, strength, and system testing on medical devices Work with tubing and small mechanical components Set up and maintain test equipment; perform basic troubleshooting Document test results and communicate findings to engineers Support calibration and quality documentation requirements Qualifications Associate degree or equivalent hands-on experience 1+ year experience in technical, lab, R&D, or manufacturing role Strong mechanical aptitude and troubleshooting skills Ability to follow procedures and document work accurately Medical device or regulated environment experience preferred.

Carlisle Weatherproofing Technologies (CWT) is a leading building envelope solution supplier that effectively drives energy efficiency and sustainability in commercial and residential applications. We are seeking a QC Tech in our East Providence, RI Plant. Job Summary Ability to perform various quality control tests on products to verify that all products meet or exceed minimum Quality Requirements. Ability to perform product inspections on Heading, Stamping, Escomatics, Heat Treating Departments and Supplier deliveries and shipping departments to ensure quality products are produced and shipped out to the customer. Standard work week 40 hours a week with occasional overtime, no travel required. Duties and Responsibilities: * Inspect materials, products, or equipment to detect defects * Use dimensional measuring devices to ensure products meet job order specifications or equipment to detect defects or malfunctions. * Enter all test results into company database and manage documents. * Communicate quality issues with Quality Supervisor, Production, Shipping and scheduling daily. * Enforce safety regulations. * Contribute to root cause analysis regarding quality issues, identify and implement appropriate corrective actions. * Creating and following up with non-conformance reports * Creating Certificates of Conformance for customer shipments when required * Assist internal quality audits. * Assist Production teams with process changes, quality plan documentation, and test requirement updates. * Generate SOP's, inspection Reports and Work Instructions as needed * Help to drive continuous quality improvement and scrap reduction across the site. * Perform quality assurance tests and visual inspections of raw materials, intermediary products, and finished goods per work instructions. * Other duties as assigned Required Knowledge/Skills/Abilities: * Math Skills proficiency up to Algebra and Trigonometry. * Must demonstrate safe working practices and possess great attention to detail. * Ability to follow CWT's policies, procedures, and process * Good communication, organization, and time management skills (multi-tasking). * Basic computer, mathematics, and problem-solving skills; ability to use a calculator. * Ability to use measuring devices (gauges, tapes, rulers, Optical Comparator, Thread gages, Hardness Testers). * Team player able to follow instructions from both management and peers. * Ability to learn and operate new equipment as needed. * Working knowledge of ISO9001:2015 Quality Management System and ISO14001 Environmental Management System (min 1-2 years Preferred). Education and Experience: * Required: * Education - High School diploma or GED required. * 1-2 years related experience required. Working Conditions: * This position conducts its work in a manufacturing environment with exposure to some odors. Use of the following equipment in the course of the job duties: * Universal testing machine. * Power Tools. * Dimensional measuring devices. * Tape Measure. * Moisture Meter. Hardness Tester * Forklift/Clamp Truck. * Computer and Phone. Personal Protective Equipment (PPE) Used: * Eye and hearing protection is required at all times on the production floor. * Safety toe shoes (steel/composite) * Hi-Vis Vests * Other PPE as defined by management within assigned department. BENEFITS AND PERKS Our employees' well-being is crucial to Carlisle's success. Despite the nationwide increase in healthcare costs, Carlisle has maintained the same employee premiums for four consecutive years by absorbing the rising medical insurance expenses. Furthermore, you have the flexibility to tailor a benefits program that perfectly suits your needs. Benefits offered: * Medical, Dental, and Vision insurance- DAY 1 * Life and Accidental Death & Dismemberment Insurance * Leave & Disability Income Protection (FMLA, LOA, PPL, STD, LTD) * Employee Assistance Program (EAP) * Health Advocate - health care concierge service * PTO - sick days, 11 holidays, vacation * 401K Retirement Savings Plan with company match * Employee Stock Purchase Plan * Flexible Spending accounts (commuter benefits, flexible spending accounts, health savings account) * College Scholarships for Dependents * Tuition Reimbursement Job Summary Ability to perform various quality control tests on products to verify that all products meet or exceed minimum Quality Requirements. Ability to perform product inspections on Heading, Stamping, Escomatics, Heat Treating Departments and Supplier deliveries and shipping departments to ensure quality products are produced and shipped out to the customer. Standard work week 40 hours a week with occasional overtime, no travel required. Duties and Responsibilities: * Inspect materials, products, or equipment to detect defects * Use dimensional measuring devices to ensure products meet job order specifications or equipment to detect defects or malfunctions. * Enter all test results into company database and manage documents. * Communicate quality issues with Quality Supervisor, Production, Shipping and scheduling daily. * Enforce safety regulations. * Contribute to root cause analysis regarding quality issues, identify and implement appropriate corrective actions. * Creating and following up with non-conformance reports * Creating Certificates of Conformance for customer shipments when required * Assist internal quality audits. * Assist Production teams with process changes, quality plan documentation, and test requirement updates. * Generate SOP's, inspection Reports and Work Instructions as needed * Help to drive continuous quality improvement and scrap reduction across the site. * Perform quality assurance tests and visual inspections of raw materials, intermediary products, and finished goods per work instructions. * Other duties as assigned Required Knowledge/Skills/Abilities: * Math Skills proficiency up to Algebra and Trigonometry. * Must demonstrate safe working practices and possess great attention to detail. * Ability to follow CWT's policies, procedures, and process * Good communication, organization, and time management skills (multi-tasking). * Basic computer, mathematics, and problem-solving skills; ability to use a calculator. * Ability to use measuring devices (gauges, tapes, rulers, Optical Comparator, Thread gages, Hardness Testers). * Team player able to follow instructions from both management and peers. * Ability to learn and operate new equipment as needed. * Working knowledge of ISO9001:2015 Quality Management System and ISO14001 Environmental Management System (min 1-2 years Preferred). Education and Experience: * Required: * Education - High School diploma or GED required. * 1-2 years related experience required. Working Conditions: * This position conducts its work in a manufacturing environment with exposure to some odors. Use of the following equipment in the course of the job duties: * Universal testing machine. * Power Tools. * Dimensional measuring devices. * Tape Measure. * Moisture Meter. Hardness Tester * Forklift/Clamp Truck. * * Computer and Phone. Physical Requirements: OCCASIONALLY FREQUENTLY CONTINUOUSLY (0-30%) (31-60%) (61-100%) LIFTING OR CARRYING * 1-10 LBS X * 11-20 LBS X * 21-40 LBS X * 41-50 LBS X * 51 OR MORE LBS PUSHING OR PULLING: * 1-40 LBS X * 41-50 LBS X * 51 OR MORE LBS X BENDING OR STOOPING X REACHING ABOVE SHOULDER LEVEL X DRIVING AUTOMATIC EQUIP. VEHICLES X OPERATE MACHINERY OR POWER TOOLS X CLIMBING (LADDERS, STAIRS, ETC.) X X WALKING X STANDING X SITTING X WORKING IN EXTREME TEMPERATURES X REPETATIVE MOTION INCLUDING BUT NOT LIMITED TO: WRISTS, HANDS AND/OR FINGERS) X X VISION X HEARING X DEXTERITY X HAND EYE COORDINATION X Personal Protective Equipment (PPE) Used: * Eye and hearing protection is required at all times on the production floor. * Safety toe shoes (steel/composite) * Hi-Vis Vests * Other PPE as defined by management within assigned department.

JOB TITLE: Quality Technician DEPARTMENT: Quality REPORTS TO: Quality Assurance Supervisor PAY: $21.00 - $23.00 per hour HOURS / SHIFT: 1st Shift / 5:30am - 2:00pm BENEFITS & PERKS: Finlays Solutions is committed to supporting the career advancement and wellbeing of our employees. We offer a range of comprehensive benefits, including a wellness program, learning and development allowance, and opportunities for mentorship and job shadowing, designed to support both personal and professional growth. We encourage continuous learning, collaboration, and the exploration of new skills and career pathways, helping you build a global network and thrive within an inclusive, supportive environment in our organization. Other employee benefits include: Health, Dental, and Vision Insurance 401(k) Company Matching Eligibility for Monthly / Annual Bonuses Paid Time Off (PTO) plus 10 Paid Holidays and Paid Volunteer Days Off Volunteer / Community Involvement DESCRIPTION: The Quality Technician will provide logistical support of the Food Safety and Quality Assurance Department and quality related aspects of the Production Department. Inspect all areas of facility and grounds to ensure constant compliance with GMP's, SSOP and HACCP Procedures. Maintain databases and other documentation required for Quality Assurance. Performs laboratory testing in support of Quality Assurance and Food Safety. Each responsibility is performed in accordance with food safety procedures. ABOUT US: Since 1750, Finlays Solutions has been the trusted leader in supplying tea, coffee, and botanical extracts to the world's leading beverage brands. Focused on delivering exceptional beverage solutions, we empower our customers to create moments of joy with every sip. Our team is built on values of acting for the long-term, taking accountability, doing better each time, and succeeding together. When you join us, you're not just taking on a job; you're becoming part of a customer-centric culture driven by collaboration, expertise, and innovation. If you're looking for a place to grow, share your ideas, and make an impact, we'd love to have you on our team. RESPONSIBILITIES: Work involves some irregular work schedule. Must be able to lift and routinely carry up to 35 pounds. Required to stand or walk up to 100% of the duty time. Requires some bending and stooping Will be recognized by all staff as having authority and accountability delegated by the Food Safety and Quality Assurance Manager and as specified in written procedures and plans to guide staff in duties related to Food Safety and Quality Assurance. Maintains databases and other documentation related to the department for the purposes of monitoring, evaluating, tracking, and trending interdepartmental data and to ensure constant compliance with standards, specifications, and regulatory requirements. Provides logistical support to ensure accurate labelling of finished goods in accordance with regulatory and customer requirements. Conducts and records laboratory testing to verify conformance to established standards and confirmation that critical control points do not exceed critical limits as established in HACCP Plans. Respond to all non-conformances to apply corrective actions and implement preventative measures. Respond to Production, Quality Assurance and Food Safety concerns by reporting problems to the Quality Assurance Manager. TESTING/ANALYSES TYPICAL RESPONSIBILITIES: Logs, processes, and tracks samples. Conducts qualitative and quantitative physical testing. Evaluate materials for compliance to standards and specifications. Operates laboratory equipment, such as analytical balances, pH meters, brix meters, water activity meters, and ATP meters. Prepare standard solutions for calibration and analyses. EQUIPMENT OPERATION AND MAINTENANCE TYPICAL RESPONSIBILITIES: Learn to evaluate methods and instrument operation problems and to review or analyze test results to locate malfunctions or inconsistencies. Maintains and calibrates lab equipment. Maintains supply of solutions, reagents and other lab testing materials. Must be able to make decisions pertaining to acceptance and rejection of manufactured goods. Hold or release of goods. Halting or allowing production. Application of corrective actions and preventive measures. QUALIFICATIONS & REQUIREMENTS: Bachelor's Degree: Degree Preferred. Experience in food processing or related field is preferred. Professional Experience: 1-2 years working experience in Quality and Food Safety Systems, ideally in a Food Safety Team Leader role. Other Working Experience: Experience in the food and beverage industry preferred. WORK ENVIRONMENT & PHYSICAL REQUIREMENTS: Work Environment: Onsite position in Lincoln, RI manufacturing facility Food processing/manufacturing environment Laboratory setting for testing and analyses Inspection of all facility areas and grounds Irregular work schedule required Physical Requirements: Must be able to lift and routinely carry up to 35 pounds Required to stand or walk up to 100% of duty time Requires some bending and stooping Ability to move throughout facility for inspections and quality checks Ability to operate laboratory equipment (analytical balances, pH meters, brix meters, water activity meters, ATP meters) EQUAL OPPORTUNITY STATEMENT: Finlays Solutions is an equal employment opportunity employer seeking diversity in qualified applicants for employment. All applicants will receive consideration for employment without regard to race, ethnicity, color, gender, gender identity, age, religion, national origin, ancestry, disability, perceived disability, medical condition, genetic information, veteran status, sexual orientation, or any other protected status, as defined by applicable law. Finlays Solutions employs individuals that are 18 years of age or older. This position is not eligible for Visa Sponsorship.

Job DescriptionDescription: About Quantic Evans: Quantic Evans is a proud member of the Quantic™ Electronics Family.Quantic™ Electronics, an electronic component company, is a trusted partner in military, aerospace, industrial, and commercial markets with over a century of combined experience as a reliable problem-solver. Being part of Quantic's portfolio has allowed Quantic Evans to continue developing cutting-edge capacitor technology alongside other world-class technology companies representing mission-critical electronics' future. With sites in East Providence, RI, and Sanford, ME, Quantic Evans manufactures high-energy density capacitors for demanding mission-critical applications. We have the most power-dense capacitor technology in the industry. We are routinely specified for defense, aerospace, and energy exploration applications where high reliability and SWAP (space, weight, and power) savings are critical design considerations. Quality Screening Technician 1, East Providence, RI Reporting to the Customer Quality Manager, the Quality Screening technician will be responsible for testing and inspecting capacitors and capacitor banks made by Quantic Evans, ensuring they meet order specifications and quality standards. Expected Hours: Full time Monday to Friday 6:00 AM to 2:30 PM Responsibilities: Product Reliability Tester (45%): Perform long-term reliability testing on assemblies, including life, thermal exposure, vibration, voltage surge testing Perform continuous monitoring testing on assemblies including fine leak test and shock. Perform special screening of finished assemblies in accordance with customer requirements. Perform electrical and functional tests on capacitor assemblies and capacitor banks for capacitance, Equivalent Series Resistance (ESR), and Direct Current Leakage (DCL). Use testing equipment to diagnose issues and ensure product functionality. Document test procedures and results. Customer Quality Support (40%): Compile and provide data for Lot Acceptance Test (LAT) reporting by the Customer Quality Manager. Research shipped product history including production records, serial/lot numbers, and test records to support customer specific inquiries. Coordinate customer returns including logging, tagging and preparation of returned products for evaluation and analysis. Work with Customer Quality Manager and Engineering to identify defects/failure modes of products Provide input for problem solving reports and organize supporting materials. In-Process Inspector (15%): Monitor production processes and perform regular quality checks. Identify and address potential quality issues during manufacturing. Work closely with production teams to implement quality improvements. Additional duties as assigned Requirements: Criteria For Success Must be considered a U.S. Person eligible to work in the United States Requires 1 to 3 years of inspection experience in a manufacturing environment. High school diploma or Equivalent, Technical school preferred Ability to read and write in English Ability to communicate in English Knowledge and understanding of scientific/ engineering notation. Capability to set up and use test equipment and measuring tools such as calipers, micrometers, indicators, multimeters, megohmmeters, and precision impedance meters. Prior experience with ISO 9001 and / or AS9100 standards desired Must possess a collaborative team-oriented mindset and personality with a hands-on, can-do attitude. Excellent organizational skills and attention to detail. Microsoft Windows and Office suite (Excel, Word) Work Environment and Physical Demands: General office and manufacturing environment. Exposure to hazards associated with manufacturing equipment and tools. Visual acuity for reading measurements, assembly instructions, and monitoring equipment. Requires manual dexterity and the ability to manipulate small objects. Ability to lift, push, and pull up to 20 pounds Sitting, bending, pushing, and pulling motions Requires sitting for long periods Walking to various stations or areas of the production floor. Upper body range of motion Ability to discern alarms and respond to machinery sounds, and verbal instructions in a noisy environment. Will be required to wear appropriate PPE as outlined by company safety protocols. EEO/AA Quantic is an affirmative action/equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, work-related mental or physical disability, veteran status, sexual orientation, gender identity, or genetic information. We participate in E-Verify. U.S. EXPORT CONTROLS As a U.S. defense manufacturer, [Company Name] is required to safeguard U.S. defense-related and other export-controlled articles, technologies, and services from unauthorized access, export, or re-export. The transfer of U.S. export-controlled articles, technologies, or services (including manufacturing processes) to individuals or entities that do not qualify as “U.S. persons,” as defined by 22 CFR 120.62, is prohibited without prior authorization from the appropriate U.S. government agencies, such as the Department of State's Directorate of Defense Trade Controls (DDTC). Under 22 CFR 120.62, a “U.S. person” is defined as a lawful permanent resident as per 8 U.S.C. 1101(a)(20), or a protected individual under 8 U.S.C. 1324b(a)(3). It also includes any corporation, business association, partnership, society, trust, or other entity that is incorporated to do business in the United States, as well as governmental entities at the federal, state, or local levels. It does not include foreign persons as defined in § 120.63. To ensure compliance with U.S. export control regulations, candidates for this position are required to undergo an Export Compliance Assessment. As part of this process, candidates may be asked to provide documentation verifying their status as “U.S. persons” or “foreign persons,” in accordance with U.S. regulation, to determine whether prior authorization is required to perform specific job duties related to this position

1253 W Central Street, Franklin, Massachusetts 02038 Work Shift: 8hr-3rd Shift (United States of America) The Quality Technician will audit, test and measure finished goods to ensure customer standards are met as well as follow our company's Good Manufacturing Practices. JOB SUMMARY: The Quality Technician will audit, test and measure finished goods to ensure customer standards are met as well as follow our company's Good Manufacturing Practices. ESSENTIAL DUTIES & RESPONSIBILITIES: * Ensure compliance with corporate and plant safety standards and with applicable laws and regulations issued by regulatory agencies. * Apply statistical tools and techniques to monitor plant performance and finished goods. * Complete laboratory testing and collect samples at established intervals. * Continually seek process improvements and make recommendations to management. * Audit compliance with GMP policies. * Performs process inspections during molding, packaging and loading. * Audit for compliance to control plan requirements including process parameters. * Perform incoming inspection of raw materials. * Complete dimensional checks and report on product. * Perform in-process inspections of manufactured product during molding, packaging and loading. * Perform cycle counts and/or inventory of finished goods as required. * Communicate quality issues and out of specifications conditions to appropriate personnel and with shift leaders. * Other duties as assigned by management. * Reasonable mandatory overtime may be required due to business needs. Qualifications: The requirements listed below are minimum requirements for the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education and/or Experience: * The technician position requires a high school diploma or its equivalent. * One year of related experience. * ASQ certification or equivalent preferred Competencies: * Safe work practices * Influencing skills * Knowledge of basic statistics * Metrology skills including calibration * Able to manage multiple priorities & meet deadlines * Good computer skills * Uses logical approach to problem solving in Production & Continuous Improvement * Understands the role of Quality in a manufacturing organization and a Quality Operating System Targeted Pay Range: $20.63 - $26.39 Altium Packaging, Our Culture Differentiates Us! We incorporate our Guiding Principles into all aspects and at all levels of the organization and use them as a framework for decision-making. We believe our Guiding Principles foster a culture of excellence that benefits both employees and customers. Our Guiding Principles * Act with Integrity & in Compliance * Drive Value Creation * Be Disciplined Entrepreneurs * Focus on the Customer * Act with Humility * Treat others with Dignity and Respect * Seeking Fulfillment in your Work We Believe in Rewarding our Most Important Resource - Our People! We show our commitment to Total Rewards by providing a competitive, comprehensive benefits package. In addition to medical, dental and vision plans, company holidays and vacation days, tuition reimbursement, learning and training opportunities, bonus potential, and a 401(k) plan with company contributions, Altium Packaging locations offer rewards and recognition programs and opportunities to make a difference in the community. EEO Statement We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, and basis of disability or any other federal, state or local protected class. Take your career to the next level at Altium Packaging!

Job DescriptionAbout UFP MedTech: UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company's single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: Medical, Dental, Vision, Life, Disability Insurance 401K with a matching contribution Paid time off, Paid holidays, Employee discounts and much more! Location: This position will be on-site full-time in Chicopee, MA. The position holder will need to be within commuting distance (within 45 min). Quality Technician Summary: The Quality Technician performs diversified duties to monitor and ensure the proper quality testing of company products. This role provides support related to corrective action containment, component measurement / testing, product certification and administrative tasks. Quality Technician Essential Duties and Responsibilities: Audits quality testing and documentation completed by operators, and reviews quality testing results to ensure proper testing has been conducted, results properly recorded and that results are within specification and without documentation errors. Reads, reviews and interprets statistical run charts to detect trends in product quality line fall-off and report to appropriate personnel. Ensures all ISO or other quality standards and procedures are being followed. Authorizes release of finished goods based on quality audits. Participates in Root Cause Investigations and provides corrective actions to customer SCARs. Conducts any required special testing, failure analysis, etc. Provides instruction, guidance and direction for manufacturing employees in determining acceptable products. Performs regularly scheduled calibration of measuring and test equipment and arrange external calibration services. Performs all other duties as assigned or needed. Quality Technician Qualification Requirements: High school diploma, and 2+ years of related work experience. Experience with Quality Standards - ISO 9001 and / or ISO 13485. Bi-lingual in Spanish strongly desired. Able to read and understand blueprints and other specifications. Able to use micrometers, calipers, video measuring equipment and other common inspection tools. Basic knowledge interpreting SPC control charting. Ability to interact with different levels of the organization. Strong oral communication and interpersonal skills. Experience with Microsoft Office applications. UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #MEDTECH #CHIC

Daily follow-up of supplier-related quality issues on the shop floor - Identification and documentation of defects and non-conformances - Taking photos and videos to support quality records and reporting - Supporting and monitoring supplier rework activities on site - Liaising with Quality and Manufacturing teams to close quality issues - Supporting basic root-cause and problem-solving activities - Ensuring quality and safety compliance within the factory environment We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to ********************.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: **************************************************** Skills and Requirements Previous experience in a manufacturing or shop-floor quality role - Experience in HVDC, power transformers, or heavy electrical equipment is desirable - Strong attention to detail and a hands-on working approach - Confident working directly on the shop floor - Basic computer skills (Word, Excel, PowerPoint) - Able to work independently and communicate clearly with multiple stakeholders

Element has an opportunity for a Cleanroom Quality Technician. The Cleanroom Quality Technician is responsible to ensure that all company and customer technical and regulatory requirements are followed within the Precision Cleaning Division. This person will be responsible to ensure processing tanks are cleaned, filtered and meet specification requirements by performing weekly titrations. Cleaning of the cleanroom will be performed on a daily, week, monthly basis to help prevent and eliminate potential risk of foreign object debris. Documents corresponding with each machine will be collected, scanned and organized on a monthly basis. All duties will be communicated with the department manager. Salary: $20- $24/hr DOE Responsibilities Essential Duties and Responsibilities include the following. Other duties may be assigned. • Administers and inventories the certifications of purchased items. • Back up for review & approve PCD finished job certifications. • Works with crafts to dispose of unwanted chemicals and supplies. • Performs a daily, weekly and monthly cleaning of the certified Cleanroom. • Change chemical tanks periodically throughout the week as per schedule. • Is responsible for keeping quality records organized and easily located on company's servers. Administer and perform: • PCD Preventive Maintenance program. • PCD Calibration program. • Updates of the PCD “uncontrolled” within the quality masters' folders. Skills / Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Common knowledge of basic hand tool use. Microsoft Office Skill are a plus. Lifting of up to 25 lbs. is expected. Mechanical aids are available for weights over 25 lbs. Will be exposed to mild alkaline and acidic based detergents and organic solvents. Company Overview Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to ‘Make tomorrow safer than today'. When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access. While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development. Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization. Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming “the world's most trusted testing partner”. All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws. The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c) “If you need an accommodation filling out an application, or applying to a job, please email ***********************”

Job Description Join the worldwide leader in playing cards and in “play” solutions. Play is what keeps us going, and it always has been our greatest motivation. That's why we live different, play different. The Quality Technician Level 2 plays a crucial role in maintaining the high standards in the production process. They utilize their skills and knowledge to inspect products or processes to ensure they meet predefined specifications and recommend improvements with the goal of delivering high quality products to our customers. What You'll Do as a Quality Technician Level 2: Complete visual and or mechanical inspections of product and processes Use measuring instruments, along with fixtures and gauges to determine product quality. Perform essential functions of In-Process, Final Assembly, and Incoming inspections including recording inspection data to the specified documents or electronic data bases. Perform defect tracking and analysis to ensure appropriate corrective actions are implemented upon identification of a defect. Use sampling plans to determine the correct samples required from a Lot of product. Process audit data and DMR's electronically in the ISO9001 ISIR Corrective Action System. Perform Finished Goods Warehouse audits. Perform all aspects of the FEP Samples Assembly process and QSAM audits process. Technicians are required to be knowledgeable in Q-S.A.M. work instructions. We're Looking for a Quality Technician Level 2 with: Previous experience as a Quality Technician Knowledge of sampling plans for inspection Functional knowledge of calibration requirements, preferably related to games manufacturing Understanding of systems used to submit product samples for toxicity & certification testing. Trained to use instrumentation and ability to record the measured data. Computer skills to recording required inspection data Solid knowledge of the ISO9001 ISIR Corrective Action System. Ability to transition easily within any of the Quality areas related to this facility. Benefits a The Quality Technician Level 2 Can Expect from Cartamundi: Competitive pay Climate controlled facility 401(k) with company match Health, dental, and vision insurance starting day one HSA (Health Savings Account) and FSA (Flexible Savings Account) Life insurance Short-Term and Long-Term Disability Paid time off Tuition reimbursement Employee discounts on daycare, gym memberships, travel, and much more Physical requirements and working conditions: Our manufacturing Plant is comprised of enclosed office and manufacturing space. This position requires the ability to: Move throughout the entire facility to attend to various issues Work effectively in teams across functional groups with strong communication skills Perform sedentary work on computer systems Lift and transfer materials weighing up to 25 pounds frequently Bend, reach shoulder height, push and pull This Quality Technician Level 2 position is located on-site in our East Longmeadow Facility Apply today and discover the magic of making a difference at Cartamundi! Cartamundi does not discriminate based on race, sex, color, religion, age, national origin, marital status, disability, veteran status, genetic information, sexual orientation, gender identity or any other reason prohibited by law in provision of employment opportunities. This employer participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. For more information on E-Verify, or if you believe that your employer has violated its E-Verify responsibilities, please contact DHS dhs.gov/e-verify . Candidates must be 18 years old to work for Cartamundi. About Cartamundi: At Cartamundi, we're all united by our common belief that world is better with play. Play is what keeps us going, and it always has been our greatest motivation. That's why we live different and play different. To us, it is not just an activity. It is a guiding mindset that reminds us to have fun, to be fair, to connect with people - across cultures and generations - and to embrace shared experiences. We are a worldwide leader in playing cards and in “play” solutions. Our owned brand portfolio includes a suite of heritage brands which go back as far as 1848, including global brands like Bicycle , HRO , Bee , Copag , Shuffle and many locally loved brands. These brands combine craftsmanship with innovation as the basis for their continued relevance and positive contribution to the local communities that love and use these brands. At Cartamundi, we have significant expertise in printing; our presses have been running since 1765. Today, our company has become the largest playing cards and board game manufacturer in the world and the trusted partner of leading toy companies. We make well-known brands such as Monopoly , Uno , Magic: The Gathering , Guess Who , Pokémon , Trivial Pursuit every day. As we look into the future and how entertainment evolves, we are bringing the digital world to the physical world and vice versa. We have a dedicated team of experts that is looking into future technologies, products, applications that can get our consumers and communities to truly live different and play different. We are still a family-owned company with headquarters in Belgium and have a global network of 16 manufacturing facilities, 6 design centers, 1 digital studio and 1 global R&D center.

Element has an opportunity for a Cleanroom Quality Technician. The Cleanroom Quality Technician is responsible to ensure that all company and customer technical and regulatory requirements are followed within the Precision Cleaning Division. This person will be responsible to ensure processing tanks are cleaned, filtered and meet specification requirements by performing weekly titrations. Cleaning of the cleanroom will be performed on a daily, week, monthly basis to help prevent and eliminate potential risk of foreign object debris. Documents corresponding with each machine will be collected, scanned and organized on a monthly basis. All duties will be communicated with the department manager. Salary: $20- $24/hr DOE Responsibilities Essential Duties and Responsibilities include the following. Other duties may be assigned. * Administers and inventories the certifications of purchased items.• Back up for review & approve PCD finished job certifications.• Works with crafts to dispose of unwanted chemicals and supplies.• Performs a daily, weekly and monthly cleaning of the certified Cleanroom.• Change chemical tanks periodically throughout the week as per schedule.• Is responsible for keeping quality records organized and easily located on company's servers. Administer and perform:• PCD Preventive Maintenance program.• PCD Calibration program.• Updates of the PCD "uncontrolled" within the quality masters' folders. Skills / Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Common knowledge of basic hand tool use. Microsoft Office Skill are a plus. Lifting of up to 25 lbs. is expected. Mechanical aids are available for weights over 25 lbs. Will be exposed to mild alkaline and acidic based detergents and organic solvents. Company Overview Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to 'Make tomorrow safer than today'. When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access. While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development. Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization. Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming "the world's most trusted testing partner". All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws. The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c) "If you need an accommodation filling out an application, or applying to a job, please email ***********************"

Cooling performance limits high-power computing, semi-conductor fab, cell networks, photonics, power electronics, and most of our digital world. Alloy Enterprises enables customers to break through these constraints with novel complex metal components that dramatically improve heat dissipation in high-performance systems. Alloy's patented Stack Forging™ process enables complex micro-geometries, resulting in single-piece, leak-tight parts that deliver superior cooling performance, lower pressure drops, and exceptional reliability. Founded in 2020, Alloy is a 55-person hardtech startup that has raised over $50M in capital and is shipping components to customers manufacturing servers, lasers, semiconductor equipment, and defense systems. About the role Alloy is seeking an experienced and dynamic Quality Technician, who will be responsible for supporting the quality assurance and control processes by conducting product inspections, testing materials and components, documenting results, and ensuring compliance with internal and external quality standards. The ideal candidate will demonstrate strong attention to detail, a proactive approach to problem-solving, and familiarity with inspection tools and methods. This role generally requires 5 days onsite per week. Responsibilities *Responsibilities are subject to change based on shifting business needs Perform in-process and final inspections on products, materials, and components. Conduct routine testing using measuring instruments (e.g., calipers, micrometers, gauges). Document inspection results and test data accurately and completely. Identify non-conforming materials or products and initiate non-conformance reports (NCRs). Support root cause analysis and corrective/preventive actions (CAPA). Maintain and calibrate inspection and test equipment. Assist with audits, including ISO or customer audits, by preparing relevant documentation. Interpret engineering drawings, technical specifications, and work instructions. Work collaboratively with production and engineering teams to resolve quality issues. Participate in continuous improvement initiatives. Other quality tasks as needed or assigned. Requirements High school diploma or equivalent; associate degree or technical certification preferred. 1-3 years of experience in a quality inspection or technician role (manufacturing environment preferred). Knowledge of ISO 9001 quality control standards preferred Proficient in using measuring and inspection tools and reading technical drawings. Basic understanding of statistical process control (SPC) and sampling techniques. Strong computer skills, including Microsoft Excel and quality management software. Excellent attention to detail and organizational skills. Familiarity with GD&T (Geometric Dimensioning and Tolerancing) preferred. Additional requirements This position will require access to information subject to control under U.S. export control laws and regulations, including the Export Administration Regulations (“EAR”) and International Traffic in Arms Regulations (“ITAR”). Please note that any offer for employment will be conditioned on authorization to receive controlled items without sponsorship for an export license. Regarding Sponsorship Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa, including H-1B, H-1C, H-2A, H-2B, H-3, F-1 or OPT at this time. Equal employment opportunity We are committed to creating an equitable and inclusive environment for all our employees and seek to build a team that reflects the diversity of the people we hope to serve with our products. We are proud to be an equal opportunity employer.

About UFP MedTech: UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company's single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: * Medical, Dental, Vision, Life, Disability Insurance * 401K with a matching contribution * Paid time off, Paid holidays, Employee discounts and much more! Location: This position will be on-site full-time in Chicopee, MA. The position holder will need to be within commuting distance (within 45 min). Quality Technician Summary: The Quality Technician performs diversified duties to monitor and ensure the proper quality testing of company products. This role provides support related to corrective action containment, component measurement / testing, product certification and administrative tasks. Quality Technician Essential Duties and Responsibilities: * Audits quality testing and documentation completed by operators, and reviews quality testing results to ensure proper testing has been conducted, results properly recorded and that results are within specification and without documentation errors. * Reads, reviews and interprets statistical run charts to detect trends in product quality line fall-off and report to appropriate personnel. * Ensures all ISO or other quality standards and procedures are being followed. * Authorizes release of finished goods based on quality audits. * Participates in Root Cause Investigations and provides corrective actions to customer SCARs. * Conducts any required special testing, failure analysis, etc. * Provides instruction, guidance and direction for manufacturing employees in determining acceptable products. * Performs regularly scheduled calibration of measuring and test equipment and arrange external calibration services. * Performs all other duties as assigned or needed. Quality Technician Qualification Requirements: * High school diploma, and 2+ years of related work experience. * Experience with Quality Standards - ISO 9001 and / or ISO 13485. * Bi-lingual in Spanish strongly desired. * Able to read and understand blueprints and other specifications. * Able to use micrometers, calipers, video measuring equipment and other common inspection tools. * Basic knowledge interpreting SPC control charting. * Ability to interact with different levels of the organization. * Strong oral communication and interpersonal skills. * Experience with Microsoft Office applications. UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #MEDTECH #CHIC