Quality assurance technician jobs in Worcester, MA

The Compliance Specialist CMC, Quality Assurance will perform critical QA tasks in support of GMP and non-GMP manufacturing programs and Regulatory Submissions at Client. The successful candidate will foster data integrity, quality and compliance across a broad range of Quality Assurance areas and will work closely with talented counterparts at Client to help ensure high quality standards and value delivery for our patients. Essential Duties and Responsibilities include, but are not limited to, the following: Performs QA review of executed development studies intended for regulatory submissions, included but not limited to draft batch records, analytical test records, and calibration records to ensure Developmental studies are conducted and data collected in compliance with approved protocols, appropriate Corporate guidelines, internal procedures, domestic and global regulatory guidelines and standards. Identifies and reports documentation errors and deviations from Protocols, SOPs or specifications in a timely manner. Responsible for communicating QA review, audit results and reporting. Collaborates with cross-functional stakeholders regarding quality events, ensuring quality records are clearly written and technically sound with supporting evidence. Qualifications: BS/BA in Life Sciences, Engineering, or Chemistry, with 2-3 years of related Quality Assurance experience within GMP-regulated industry, or 1-2 years with Masters degree. In lieu of a Life Sciences degree, consideration will be given to candidates with minimum of 6+ years of industry experience in biotechnological and/or pharmaceutical quality, manufacturing, or other industry requiring high technical aptitude and attention to detail.

As a Process Technician, you operate equipment to manufacture plastic containers for leading consumer brands. At our company, we take pride in maintaining our high standards for quality products & a positive team culture. We're also proud to be recognized as an America's Safest Companies by EHS Today. We Offer Set Schedules: 12-hour shifts & a rotating 2-week standard schedule of 3 days, then 4 days is 15 working days a month as a full-time associate! Stability & Growth: We follow a strong promote-from-within business practice and offer a stable job through current market uncertainty! Stability: Our business is prosperous and we're not laying off - we're hiring! Advancement: We prioritize promotion from within! You Will Operate a variety of top-of-the-line extrusion & blow-molding manufacturing equipment in a clean, safe & climate-controlled environment Monitor equipment, making adjustments to settings (heat control, water cooling temperatures, hydraulic pressure, etc.) to produce high-quality rigid plastic containers Troubleshoot equipment & perform routine preventative maintenance Assure Plastipak customer requirements are met by performing quality checks for specifications, such as bottle weights & dimensions Join with your team to identify continuous improvement opportunities focused on safety, reliability, quality & scrap reduction Grow your skills through formal & side-by-side training, and have opportunities for career advancement You Have Ability to work the following schedule: 6:45 pm - 7:15 am on a cycle of 3 days on, 2 days off, 2 days on, 3 days off, repeat. This equates to 2 weekends per month off with a 3-day weekend High School Diploma, GED or equivalent A minimum of one (1) year of experience as a Manufacturing Production Technician working with equipment used for high-volume production Working knowledge of extrusion or blow molding equipment is preferred Hydraulics, pneumatics & electrical mechanical basic knowledge Ability to troubleshoot & problem solve Ability to lift up to 50 pounds with or without a reasonable accommodation You'll Earn $18.40 & up, based on experience Night shift includes a shift differential of $.50 As a Plastipak Associate, you receive a benefits package offering the following: Wellness Programs Health Insurance Coverage, including Medical, Dental & Vision EAP, Employee Assistance Program Life Insurance Accidental Death & Dismemberment Insurance Disability Insurance: Short-Term & Long-Term Accidental Insurance Critical Illness Insurance Hospital Indemnity Insurance 401(k) Plan, with Company Matching Contribution & Profit Sharing feature Paid Time Off - 80 hours within 1st year & subsequent increases Paid Company Holidays Dependent Care Flexible Spending Account Caregiving via Care.com Pet Insurance Tuition Assistance Program Sons and Daughters Scholarship Program Travel Assistance Employee Discount Programs *Some benefits are subject to eligibility requirements Plastipak is an Equal Opportunity Employer In order to process your job application, Plastipak collects and stores the personal information that you submit via this website. Please refer to Plastipak's Privacy Policy to understand how Plastipak uses and protects the information that you provide.

Job Title: Manufacturing Quality Technician Duration: 6 + Months Pay rate: $27 - 30/hr(Without benefits) 3 Days a Week - 6pm-6am The Associate Manufacturing Technician will operate, troubleshoot, and maintain advanced automated equipment used in producing medical devices. The role involves cross-training across multiple technologies-laser welding, heat staking, PCB handling/testing, robotic automation, metal forming, discrete component assembly, and medical packaging. This position requires strong mechanical aptitude, problem-solving ability, and comfort working in a fast-paced, highly regulated manufacturing environment. Key Responsibilities Set up, operate, and perform basic maintenance on automated manufacturing equipment with minimal supervision. Monitor machines, maintain raw material feeds, clear faults/stoppages, and adjust processes using HMIs. Conduct equipment inspections; create work orders for corrective or preventive maintenance. Troubleshoot mechanical issues, ensure product quality, and use measurement tools to verify tolerances. Support new product transfer, process development, and equipment/process v alidations. Participate in issue investigation and corrective actions within equipment cells. Manage material handling, documentation, inventory updates, and follow all GMP/SOP requirements. Maintain a clean manufacturing/cleanroom environment and collaborate across teams to improve processes. Qualifications High school diploma/GED or 3+ years manufacturing experience. Basic math skills; proficient in English. Mechanical aptitude with ability to operate, debug, or maintain automated equipment. Preferred: experience with HMIs, robotics, discrete assembly, medical devices, laser/heat staking/ultrasonic welding, and cleanroom work. Familiarity with measurement tools (micrometers, calipers, gauges). Physical Requirements Standing/walking most of the shift; ability to lift up to 20 lbs. Frequent reaching, pushing, and pulling. Dexian is a leading provider of staffing, IT, and workforce solutions with over 12,000 employees and 70 locations worldwide. As one of the largest IT staffing companies and the 2nd largest minority-owned staffing company in the U.S., Dexian was formed in 2023 through the merger of DISYS and Signature Consultants. Combining the best elements of its core companies, Dexian's platform connects talent, technology, and organizations to produce game-changing results that help everyone achieve their ambitions and goals. Dexian's brands include Dexian DISYS, Dexian Signature Consultants, Dexian Government Solutions, Dexian Talent Development and Dexian IT Solutions. Visit ******************* to learn more. Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status

•Assist with laboratory testing to help diagnose various pet and other animal illnesses, injuries, and diseases; process specimens; help with a variety of laboratory tasks • Assist with lab inventory, procuring supplies, and stocking shelves. *Assist with moving samples around the lab, loading analyzers, and general lab maintenance and cleanliness • Support and maintain various processes, systems, and databases. • Perform recordkeeping ad data collection • Perform administrative duties such as answering phones and preparing parcel deliveries, files requisitions, and performs duties in support of billing, pricing, and sample transportation. What You Need to Succeed: • Ability to read and interpret documents such as safety rules, standard operating procedures (SOPs), material safety data sheets (MSDSs), operating and maintenance instructions, government rules and technical procedures. • Ability to prioritize and multi-task • Strong initiative and follow through • Attention to detail • Ability to work independently and as a team contributor • Must demonstrate a high level of customer service • Good computer skills: Microsoft Office and SAP preferred • You meet the physical requirements that go with working as a Lab Associate - May transport hazardous waste within the facility and may occasionally lift and move up to 25 pounds.

This is a full-time, onsite position for a Level I Research Laboratory Technician responsible for performing technical procedures and providing comprehensive support for research activities under minimal supervision. The role requires application of standard scientific techniques, analytical principles, and adherence to a challenging, non-traditional schedule. Title: Research Laboratory Technician I (Onsite - Northampton, MA) Location: Northampton, MA Schedule: Staggered schedule (alternates weekly): 5:45 PM EST to 6:15 AM EST (Night Shift) with Working Weekends. Equipment: No personal laptop required. Experience Level: 0-5 Years of Experience Primary Responsibilities: Technical Execution: Perform specialized tests and procedures utilizing complex laboratory equipment. Scientific Consultation: Confer with senior laboratory personnel regarding research procedures, techniques, and recommend practical modifications as needed. Data Analysis & Reporting: Execute statistical calculations, analyze experimental data, and prepare detailed reports summarizing results. Research Support: Conduct literature reviews to gather abstracts and critical information for ongoing research projects. Logistics & Procurement: Procure and order supplies, materials, and experimental components necessary for lab operations and research needs. Specialized Tasks (May Include): Supervise the care of research animals, perform minor animal surgery, or collect animal tissues and specimens for laboratory analysis. Required Qualifications: Education/Experience: Degree in a related scientific discipline (Biology, Chemistry, or other scientific fields) preferred, but equivalent work experience is accepted. Technical Knowledge: Demonstrated knowledge of complex laboratory techniques, equipment operation, scientific terminology, materials, and substances. Skills Skilled in the use of diverse laboratory equipment. Required ability to perform and analyze statistical calculations and prepare accurate technical reports. Ability to work effectively under minimal supervision.

The Quality Technician - FAI Specialist is responsible for coordinating and supporting the creation of AS9102 First Article Inspection Reports (FAIR) in alignment with industry and customer specific requirements. This position works alongside various other departments and is vital to ensuring success of the AS9102 program. Duties/Responsibilities: Navigates internal company software and database systems to gather information. Accurately completes AS9102 Reports (FAIR) and other dimensional inspection reports as required. Interpret drawings, specifications and customer requirements. Works effectively and communicates with various departments, including: Planning, Marketing, Quality, QC Inspection and Source Inspection. Assures accuracy of FAI programs and records. Assists with identifying opportunities for improvement within the FAIR process to aid in the success of the Quality Department. Maintain a positive work environment by acting and communicating in a manner so that you get along with customers, clients, vendors, co-workers and management. This position may require overtime for coverage on alternate shifts and weekends. Will be required to perform other duties as requested, directed or assigned. Requirements: High School diploma or General Education Degree (GED). Previous experience as a First Article Inspection Specialist is preferred but not required. Must be able to use a computer to maintain records, develop reports, and analyze data and document discrepancies as well as using a computer to perform all other related aspects of the position. Must have excellent communication skills and ability/flexibility to work in a fast-paced environment. Must be able to read and interpret technical drawings, prints and industry/customer specifications. Must be able to read and interpret GD&T requirements. Must be able to display a thorough attention to detail and organization. Amphenol offers a competitive salary and benefits. The candidate must be able to legally work in the United States; we are unable to provide sponsorship. Position requires candidate to be a U. S. person as defined in ITAR, 22 CFR 120. 15 (U. S. Citizenship or Resident Alien Status) and defined by 8 U. S. C. 1101(a) (20). Amphenol is a proud Equal Opportunity Employer as to all protected groups, including Individuals with Disabilities and Protected Veterans. For consideration for this position, please apply online to: ********************* acquiretm. com APC878

RELOCATION ASSISTANCE: No relocation assistance available CLEARANCE TYPE: NoneTRAVEL: NoDescriptionAt Northrop Grumman, our employees have incredible opportunities to work on revolutionary systems that impact people's lives around the world today, and for generations to come. Our pioneering and inventive spirit has enabled us to be at the forefront of many technological advancements in our nation's history - from the first flight across the Atlantic Ocean, to stealth bombers, to landing on the moon. We look for people who have bold new ideas, courage and a pioneering spirit to join forces to invent the future, and have fun along the way. Our culture thrives on intellectual curiosity, cognitive diversity and bringing your whole self to work - and we have an insatiable drive to do what others think is impossible. Our employees are not only part of history, they're making history. Northrop Grumman's Space Sector is seeking a Quality Control Technician - Level 2 to join our team in Devens, MA. This position is 100% onsite and cannot accommodate telecommute work. AOA Xinetics (AOX), a wholly-owned Northrop Grumman Space Systems Business Unit, is a leading supplier of complex electro-optic and photonic systems and subsystems that control and manipulate light waves for a variety of applications. Reporting to the Quality Manager, the Quality Control Technician - Level 2 should have technical strengths in verification of requirements specified for operations, products, processes, and documents. Must possess the ability to plan and organize work in order to effectively and successfully accomplish assigned tasks. Have the ability to work multiple programs while maintaining attention to detail. Accurately interpret drawings and specifications. Working knowledge and understanding of GD&T is essential for this role. Be strategic in the identification of technical needs and solutions coupled with a strong program execution focus. Possess excellent communication skills and effectively interface with AOX technical and non-technical department members, suppliers, and customers. This position will work a 9/80 schedule, with every other Friday off. In this job, you will: Verify optical, ceramic, and mechanical components and sub-systems. Verify electrical assemblies and wiring harnesses. Recommend verification or test methods and statistical process control procedures for achieving required levels of product compliance and reliability. Propose changes in design to improve measurement assessments, systems and/or process reliability. Review and verify optical and electrical testing methods and results. Witness and verify product performance testing. Compile data and define changes required in product design, test equipment, test procedures, manufacturing processes, or new testing requirements. Evaluate product compliance to specified requirements and readiness to release. Other assignments presented by the Quality Manager. Compile data and evaluate safety critical components and constructions in system design, equipment and procedures to mitigate risks. Develop safety documents as required to support customer and test/certification requirements. Design and implement Quality plans for use in verifying in-coming product Quality. Perform product safety and EMI testing on systems and sub-assemblies as required. Research, evaluate and qualify supplier approval requirements, perform first article qualifications, perform internal audits, monitor and manage internal and supplier corrective actions Participate in MRB as needed. Basic Qualifications: High School diploma or equivalent and 2 years additional education and/or related experience. or an Associate Degree in Quality, Manufacturing or Technology and Quality Assurance Verification No clearance required to start Operating Coordinate Measuring Machinery (CMM) Strong problem solving and collaboration skills and verbal/written communication skills Intermediate Microsoft Office skills US Citizenship is a requirement for employment Preferred Qualifications: Experience in DoD, Aerospace and/or Semiconductor Fabrication Manufacturing QC/Verification experience with optical, ceramic, and/or electro-optical sensors and systems verification, precision optics, opto-mechanical and electrical products COTs product development Experience working in or implementing Copy Exact control systems Experience in reliability prediction and in-use reliability measurements FMEA, RCCA, Risk management, or Quality auditing experience Experience implementing ISO 9000, AS9100, TL9000, TS16949, ISO 13485, and/or CMMI for Development Physical Requirements: Occasional travel to our East Harford facility and/or supplier sites for source verification or supplier evaluation Excellent hand/eye coordination and manual dexterity Ability to sit or stand for extended periods of time and light physical effort required Curious about all the exciting developments with the Northrop Grumman Space Sector? Click the link below: ************************************* Working at Northrop Grumman is more than just a paycheck. We offer a comprehensive Total Rewards and benefits package designed to help you thrive at work and in life. For more information on our Total Rewards package, please visit our Total Rewards site. Northrop Grumman Total Rewards Primary Level Salary Range: $51,400.00 - $85,600.00The above salary range represents a general guideline; however, Northrop Grumman considers a number of factors when determining base salary offers such as the scope and responsibilities of the position and the candidate's experience, education, skills and current market conditions.Depending on the position, employees may be eligible for overtime, shift differential, and a discretionary bonus in addition to base pay. Annual bonuses are designed to reward individual contributions as well as allow employees to share in company results. Employees in Vice President or Director positions may be eligible for Long Term Incentives. In addition, Northrop Grumman provides a variety of benefits including health insurance coverage, life and disability insurance, savings plan, Company paid holidays and paid time off (PTO) for vacation and/or personal business.The application period for the job is estimated to be 20 days from the job posting date. However, this timeline may be shortened or extended depending on business needs and the availability of qualified candidates.Northrop Grumman is an Equal Opportunity Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class. For our complete EEO and pay transparency statement, please visit *********************************** U.S. Citizenship is required for all positions with a government clearance and certain other restricted positions.

The primary result expected from the Quality Control Technician will be to assure product quality by preparing samples, conducting quality control inspection and testing of components, dispersions, and finished goods, determining adjustments for batches that do not conform to requirements, documenting inspections, and insuring calibration of testing equipment. Essential Duties & Responsibilities: * Perform testing of production batches, incoming raw materials, finished goods, and components to determine conformance to specifications. * Judge as "fit for release" production batches, incoming raw materials, finished goods, and components that are in conformance to all specifications and visually acceptable. * Determine and communicate batch adjustments for any batches that do not conform to requirements, utilizing batch history, adjustment guidelines, and consultation with the Senior QC Technician, Assistant Supervisor, or QC Manager. * Perform validation testing during filling to insure integrity of finished goods, including labeling, packaging, and fill weights. * Communicate current status of inspections to Senior Technicians, Assistant Supervisor, or QC Manager. * Communicate issues with work instructions and procedures to Senior Technicians, Assistant Supervisor, or QC Manager. * Document inspection results. Required Experience: * 1-3 years of production/manufacturing/quality control experience preferred but not required. * High school diploma or equivalent, Associate's or Bachelor's degree a plus * Some background in physical sciences and algebra * Ability to accurately read and enter computer data through a variety of tests * Proficiency in Excel, Word, and other MS Office applications * Experience in SAP recommended but not required Rust-Oleum is an equal opportunity employer. Employment selection and related decisions are made without regard to sex, race, age, disability, religion, national origin, color, or any other protected class.

Quality Technician I Wage: $23.65 + $2.00 shift differential shift: 2nd Shift- 2:30pm-11:00 pm From a small family business to a multi-billion dollar global company, Sonoco has been changing the face of products and packaging since 1899 - all while keeping the heart of “People Build Businesses” alive. Our talented people are at the core of our growth, constantly reinventing the Sonoco wheel with brilliant solutions every year. Today we are a world leader in global packaging solutions with diversified operations in over 34 countries. We're extremely proud of our portfolio of brands, our achievements in sustainability and industrialization and the groundbreaking work accomplished by our people. While reporting to the Quality Manager as a Quality Technician you will be require to use problem-solving techniques in routine job activities and team settings, performs all responsibilities in a manner, which ensures the quality expectations of every customer, both internal and external, are met or exceeded. Measures critical product/process variables, records or reports using appropriate tools and utilizes information to continuously improve. If unable to maintain processes within established limits or meet specifications, is fully authorized to stop the operation and seek assistance. What you will be doing: · Conduct required off-line testing for products. ·Ensure all customer feedbacks are completed on-time, root cause is identified and implemented. ·Assist in analyzing all customer feedbacks for trends and continuous improvement. · Involved in corrective action and preventive action process. ·Assist in process capability studies as deemed necessary. ·Assist and/or train plant personnel in GIQ quality system. · Assist in maintaining customer property. ·Assist in maintaining process for document control. ·Document COA's, COC's as required. ·Participates on customer visits. ·Defines quality concepts and quality processes, including statistical basics, etc.; applies quality tools; interprets information and data; applies team concepts. ·Where applicable, support the food safety team to organize its work, ensure relevant training and education of the food safety team members, ensure the food safety management system is established, implemented, maintained and updated, and report to the organization's top management on the effectiveness and suitability of the food safety management system We'd like to hear from you if: · Ability to push, pull, lift and/or carry up to 50 pounds on a frequent basis and up to 75 pounds on an occasional basis. · Ability to frequently bend, stand, stoop and grasp. · Ability to manipulate small parts on a consistent basis. ·Must know which measurement and test equipment (M&TE) tools are appropriate for various tasks and how to assess tool accuracy and precision; understands the concept of standards traceability for M&TE. ·Understands and applies basic inspection and testing techniques, including various types of sampling plans. ·Understands and applies various quality audit types and their components, tools, and techniques. ·Must be able to control nonconforming material. ·Performs miscellaneous job-related duties as assigned. At Sonoco Products Company, we offer a comprehensive total rewards package, including competitive pay and benefits. *Benefits listed below are for employees located in the U.S. Specific benefits and wellbeing programs may vary depending on your location (within the U.S. or global), or if you are a union employee. Benefits Medical, dental, and vision coverage for you and your dependents, including FSA and HSA options 401(k) retirement plan with company match Wellbeing tools and resources to support holistic health, including an Employee Assistance Program with a variety of services Paid time off and holidays to recreate, rejuvenate and care for the health of yourself and family Variety of company paid and voluntary employee-paid insurance plans including life, personal accident, and disability insurance Tuition reimbursement We are an equal opportunity employer, and we strictly prohibit and do not tolerate discrimination against employees, applicants or any other covered persons because of race, color, religion, national origin or ancestry, sex, pregnancy, sexual orientation, marital status, gender identity or expression, age, disability, genetic information, veteran status, or any legally protected characteristic.

At Spindrift, we're making every beverage a positive force of nature. Founded in 2010, we believe the best flavors come directly from nature. That's why every Spindrift beverage is made the hard way-with real squeezed fruit, never from concentrate. From sourcing the best-tasting fruit globally to maintaining a carefully honed manufacturing process, we believe in doing things the hard way, the intentional way, the better albeit more challenging way, the right way - because, in the end, it's worth it. Spindrift sparkling water is available nationwide, and Spindrift Spiked and Spindrift SODA is available in select markets. We are also a proud member of 1% for the planet, donating to environmental causes. Spindrift is headquartered in Newton, MA. The Quality Technician Role The Quality Technician will be responsible for supporting the Spindrift quality program across Spindrift's beverage portfolio, assist with maintenance of the retain library, assistance with recruiting and training internal sensory panelists, assist with collecting, synthesizing and archiving data as it relates to quality initiatives. Responsibilities include: * Assisting the Sensory Analyst with managing the Spindrift sensory program by supporting new panelist onboarding and training, product retain tastings onsite, raw material evaluations, and standard production retains * Assisting with managing the Product Retain Library to ensure it is neatly organized at all times, including maintaining an orderly process of receiving/processing product retains into the library upon arrival and the disposal/removal of out-of-date code samples * Supporting the creation and organization of quality documentation (i.e. SOPs, protocols, training documents and more as needed) * Collaborating with various teams within operations on the following activities: * Finished product releases as needed, including review of finished micro reports and sensory evaluations * Production holds as needed, including performing sensory evaluations on finished product and communicating results to relevant parties * Assist with qualification of new suppliers, including performing required sensory evaluation of raw materials to determine acceptability for use * Data entry and approval for specified raw materials into quality management system * Assist with consumer complaint process, to include but not limited to: data entry, sample collection, investigation support

Title: Operations Quality Technician Duration: 6 Months with possible extension PM shift: Friday - Sunday 6pm - 6: 30am As long as they work out, they should be converted to FTE after 90 days. The Operations Quality Technician will be a critical contributor in a mission that truly represents a once-in-a-lifetime opportunity to join a company that is making significant investments in establishing US manufacturing, expanding internationally, and delivering a consistent cadence of product innovations to the market and investing in its people. The successful candidate will be responsible for ensuring our manufacturing site produces and distributes products which meet or exceed all established quality standards and will be responsible for ensuring our processes and procedures are compliant with corporate policies and federal law. The individual will be trained in performing Incoming, In-process inspections in the cleanroom, or assessing the final product's efficacy prior to market release. In addition to those activities, this position may also be required to support production operations, metrology, microbiology, or other manufacturing functions as business needs arise. This position requires a strong attention to detail, problem solving skills, and willingness to work in a fast-paced manufacturing environment. Responsibilities: Inspect and record results of work on Incoming raw material, In-process, or Lot Qualification at various stages of the production process, distribution process to determine and maintain the quality and reliability of our product. Assess and complete inspection reports and records including the entry of data into various electronic systems. (For example -Word, Excel, SAP, Electronic DHR systems, Oracle Agile, and others). Generate, review, and maintain quality records in support of the Quality System. (For example -device history records and training records) Ensure the equipment calibration status is within the timeframe of use. Assist the Quality Manager in notified body and regulatory authority audits and inspections. Works from specifications, work plans, procedures, and general instructions from either Quality Engineers, Quality Supervisor, or the Quality Manager. Required to maintain and enforce cGMPs. Safely follow standard operating procedures including but not limited to quality standards, material handling, and record keeping. Must follow all Good Manufacturing Practices (GMPs), Good Documentation Practices (GDPs), and Good Laboratory Practices (GLPs). Notifies Quality or Operations Leadership of any discrepancies to ensure quality standards and safety of operations are maintained at all times. Maintain a clean work environment suitable for medical device manufacturing and cleanroom production. Performs other duties as required Required Skills and Competencies: Excels at the organization and maintenance records accurately. Self-starter capable of dealing with a variety of tasks in a fast paced, multi-tasking environment. Must be proficient in English language to be able to read documentation, communicate, and write. Mathematics -Basic mathematics skills (adding, subtracting, multiplying, dividing) Autonomy - Capable of working independently with minimal instruction from their supervisor. Education and Experience Minimum Requirements: High School diploma Preferred Competencies: Familiarity with measurement instrumentation such as micrometers, calipers, tensile testers, video microscopes, and optical gauging products preferred. Experience working in a lab setting environment in the medical device industry. The ability to use stereoscopes and varying microscope setups. Physical Requirements: Required to stand for up to 75% of working time per shift, with walking at least 50% of working time per shift. Required to reach above shoulder frequently and below waist occasionally. Required to push and pull. Ability to lift up to 20lbs occasionally, 5-20lbs frequently. Vision capability to inspect small parts/components/labeling (Corrective lenses allowed) Start Date - End Date: Jan 9 -Jul 7, 2026

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 #IND3

At Spectrum Control, most departments operate on a 4-day, 10-hour work schedule in exchange for a 3-day weekend. We offer competitive wages and PTO, plus our benefits begin on day 1 of employment. Come join a workforce where we put you first! JOB SUMMARY: The Quality Technician inspects and tests materials and equipment to ensure compliance with specified drawings and procedures. ESSENTIAL JOB FUNCTIONS: Verify and inspect materials to match PO and MRP requirements in accordance with specification drawings, military standards, commercial standards, sampling plans and internal procedures as required. Perform screening of materials as specified on incoming inspection travelers and/or shop travelers. Perform first piece inspection actions and completion of AS 9102 forms required under AS9100 where applicable. Inspect devices under high-powered microscopes for verification of compliance or defect identification and initiate and submit deficiency forms on any non-compliant materials as outlined by company MRB procedures. Perform functional electrical measurements using LCR meters, multimeters and other test equipment. Program, set-up and operate the coordinate measuring machine (CMM) and perform basic maintenance and calibration on the CMM where necessary. Inspect detailed machined parts and assemblies per print requirements if in a machine shop setting. Conduct first article, first piece, in process and final inspection. Ensure compliance using mechanical measuring devices including, but not limited to: calipers, dial gauges and optical comparators and facilitate testing to ensure compliance. Maintain and organize quality documentation. Maintain critical task training and certification records. Perform quality and process improvement audits and assist manufacturing inspectors with internal and external inspections as directed. Perform other inspection, testing or quality related tasks as needed. QUALIFICATIONS: Education: High School or Equivalent Experience Years: 1-3 years Experience Type: Production, Quality Related Field OR Equivalent combination of education and experience Microsoft Office and web proficiency Able to read and interpret blueprints, operating and maintenance instructions, ISO 9000 and 9001 company procedure manuals, specifications and geometric tolerancing and bar graphs Ability to do basic math in all units of measure using whole numbers, common fractions and decimals Ability to use SolidWorks software where applicable Understanding of LAN and information systems IPC-A-610 and J-STD-001, IPC 600/3012 certification in certain areas WORK ENVIRONMENT: Manufacturing Floor Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities 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) Third-Party Recruiters Please note, that per Spectrum Control Policy, we do not accept unsolicited resumes from third-party recruiters unless such recruiters are engaged to provide candidates for a specified opening and in alignment with our values and expectations. Any employment agency, person or entity that submits an unsolicited resume does so with the understanding that Spectrum Control will have the right to hire that applicant at its discretion without any fee owed to the submitting employment agency, person or entity. If you or your agency are interested in becoming an approved vendor please contact ************************************.

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.

The primary result expected from the Quality Control Technician will be to assure product quality by preparing samples, conducting quality control inspection and testing of components, dispersions, and finished goods, determining adjustments for batches that do not conform to requirements, documenting inspections, and insuring calibration of testing equipment. Essential Duties & Responsibilities: Perform testing of production batches, incoming raw materials, finished goods, and components to determine conformance to specifications. Judge as “fit for release” production batches, incoming raw materials, finished goods, and components that are in conformance to all specifications and visually acceptable. Determine and communicate batch adjustments for any batches that do not conform to requirements, utilizing batch history, adjustment guidelines, and consultation with the Senior QC Technician, Assistant Supervisor, or QC Manager. Perform validation testing during filling to insure integrity of finished goods, including labeling, packaging, and fill weights. Communicate current status of inspections to Senior Technicians, Assistant Supervisor, or QC Manager. Communicate issues with work instructions and procedures to Senior Technicians, Assistant Supervisor, or QC Manager. Document inspection results. Required Experience: 1-3 years of production/manufacturing/quality control experience preferred but not required. High school diploma or equivalent, Associate's or Bachelor's degree a plus Some background in physical sciences and algebra Ability to accurately read and enter computer data through a variety of tests Proficiency in Excel, Word, and other MS Office applications Experience in SAP recommended but not required Rust-Oleum is an equal opportunity employer. Employment selection and related decisions are made without regard to sex, race, age, disability, religion, national origin, color, or any other protected class.

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 ***********************”

About LightForce LightForce is a 3D printing technology company focused on the orthodontic space. Our digital platform empowers orthodontists with 3D-printed tooth-moving tools. In 2019, we launched our first product - the world's only, fully customized 3D printed bracket system and digital treatment software. We are proud to be one of the fastest growing companies in the industry. Learn more at: ********* Description The Quality Technician is an integral part of the Physical Manufacturing Quality Assurance Team providing hands-on support of production and engineering efforts. The ability to translate Quality Team goals into action at the operator level and to communicate day-to-day observations to the engineering and management team provides a key linkage between production processes and support staff. This role provides direction support to the Quality Engineering Team and has the opportunity to take part in a variety of project efforts. A key function of the Technician role is routine measurement of key product features as part of process inspection and control efforts. Other visual inspections and mechanical/performance tests will be expected. This position will report to the Quality Manager. We are hiring for Monday-Friday, 2nd shift 3p-11p Essential Duties and Responsibilities Conduct testing of production parts per testing protocols and work instructions with minimal supervision Perform specific tests and inspections of production parts in support of validation and continuous improvement efforts Records and documents observations during inspection, testing, and control Support investigation of customer complaints and internal non-conformances Investigate potential non-conformances and provide input for decisions of dispositioning quarantined material Aid in training and retraining of Final Inspectors and other Production Staff Education and Experience High-school education or equivalent required 0-1 years of experience working in medical device or other highly regulated manufacturing environment Required Qualifications Excellent hands-on technical skills, ability to apply advanced troubleshooting skills on the manufacturing floor Experience inspecting small parts using microscopes and/or other visual magnification aids Must demonstrate acute attention to detail and organizational skills Critical understanding of the importance of documentation and data traceability Familiarity with executing Standard Operating Procedures in a manufacturing or assembly environment Basic knowledge of computer usage, email communication, and Microsoft Office and/or Google office functions Basic understanding of acceptance testing and ability to evaluate tolerances per product specifications Fluent speaker of English with the ability to communicate technical details verbally and in writing Preferred Qualifications Post-secondary technical education or professional certifications are a plus Associates or Bachelors degree in Manufacturing is a plus Advanced experience in data analysis tools (advanced skills in Excel and others) is a plus Knowledge in Quality Management Systems is a plus Previous experience in a Quality Inspection role is a plus Physical Demands Frequent standing, walking, bending, reaching, hand, and finger manipulation Perform work activities with production chemicals, adhesives and epoxies, using required personal protective equipment Work Environment Office environment up to 90% Work is sometimes performed in an open office, sedentary position Limited temperature fluctuations, heated and air conditioned environment Work is performed near moving mechanical parts and occasionally with sensitive chemicals The noise level in the work environment is usually moderate 1st and 2nd shifts available Perks and Benefits (US employees only) Unlimited PTO for exempt employees 10 paid holidays per year Generous premium coverage for medical and dental plans Access to employee paid vision plan Group plan voluntary life insurance Fringe benefits 401k retirement plan Paid parental leave Workplace perks such as food/coffee To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. 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 liabilities. LightForce Orthodontics is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state, or local law.

Requirements Be responsible for driving and maintaining your company vehicle which you will take home with you for use during work hours Ability to communicate professionally and clearly with manager and co-workers via phone, text, email, and in-person Mechanically inclined Must have a valid driver's license with a clean driving record and be able to pass pre-employment screenings Ability to lift up to 60 pounds without assistance; up to 150 pounds with assistance Ability to sit or stand for at least 30 minutes Ability to twist and bend at the waist repeatedly Draft Line Quality Technician Benefits: (Part time positions may not include all benefits listed) Competitive Salary Commissions paid for leads generated in the field Medical/Dental/Prescription/Vision plans Paid Time Off 9 paid holidays 401(k) with generous employer match Annual boot reimbursement Employer paid benefits such as life, short-term and long-term disability insurance plans Flexible Spending Accounts (Medical, Dependent care, and Commuter) We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Salary Description $18.00 - $20.00 per hour

The primary result expected from the Quality Control Technician will be to assure product quality by preparing samples, conducting quality control inspection and testing of components, dispersions, and finished goods, determining adjustments for batches that do not conform to requirements, documenting inspections, and insuring calibration of testing equipment. Essential Duties & Responsibilities: Perform testing of production batches, incoming raw materials, finished goods, and components to determine conformance to specifications. Judge as “fit for release” production batches, incoming raw materials, finished goods, and components that are in conformance to all specifications and visually acceptable. Determine and communicate batch adjustments for any batches that do not conform to requirements, utilizing batch history, adjustment guidelines, and consultation with the Senior QC Technician, Assistant Supervisor, or QC Manager. Perform validation testing during filling to insure integrity of finished goods, including labeling, packaging, and fill weights. Communicate current status of inspections to Senior Technicians, Assistant Supervisor, or QC Manager. Communicate issues with work instructions and procedures to Senior Technicians, Assistant Supervisor, or QC Manager. Document inspection results. Required Experience: 1-3 years of production/manufacturing/quality control experience preferred but not required. High school diploma or equivalent, Associate's or Bachelor's degree a plus Some background in physical sciences and algebra Ability to accurately read and enter computer data through a variety of tests Proficiency in Excel, Word, and other MS Office applications Experience in SAP recommended but not required Rust-Oleum is an equal opportunity employer. Employment selection and related decisions are made without regard to sex, race, age, disability, religion, national origin, color, or any other protected class.