Quality control inspector jobs in Pawtucket, RI - 312 jobs

The Middlesex Corporation is a nationally recognized and award-winning leader in the heavy civil construction industry. Since 1972, the family business founded by Robert W. Pereira has developed an extensive client and project list through its consistent efforts to safely build America's infrastructure. The Middlesex Corporation specializes in building and reconstructing highways, bridges, marine, rail, and transit facilities through its collaborative team approach and focus on core values. In addition, Middlesex Asphalt in Central Florida is one of the largest and most productive asphalt plants in the United States with Middlesex Paving earning an equally solid regional presence and reputation. Position Summary: The MRM Quality Control Technician is responsible for ensuring the quality, consistency, and compliance of ready mixed concrete and aggregates produced by Massachusetts Ready Mix. This role performs routine plant and field testing, inspections, and documentation to verify materials meet applicable job specifications, Department of Transportation requirements, and industry standards. PI53309b218c6b-37***********9

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

Primary Skills: Robotics testing (Expert), Automaton Testing (Proficient), Documentation (Proficient), Test Plans (Proficient), bug management (Proficient), Contract Type: W2 Duration: 6+ months with possible extension Pay Range: $45.00 - $50.00 per hour #LP Job Summary: We are looking for a Quality Assurance Technician II to join our team, dedicated to operating and supporting robotic technology at sortation centers. This role involves executing test plans, collecting and analyzing data, and reporting results under the guidance of Test Engineers and Engineering Leads. The successful candidate will work closely with sortation center personnel to ensure the successful integration of new technologies into our product development process. Key Responsibilities: Execute test plans developed by Global Engineering Test Engineers. Collect and analyze data from testing processes to identify areas for improvement. Engage with Test Engineers, TE Manager, and Engineering Leads for guidance and direction. Collaborate with local sortation site personnel including Operations, RME, WHS, etc. Report results and findings to stakeholders and suggest recommendations for enhancements. Must Have Skills: Operate and test robotic technologies at sortation centers, supporting onboarding into RDPI's product development process Execute engineering test plans and test cases developed by RDPI Global Engineering Test Engineers Collect, analyze, and report test data and results with accuracy and clarity Work under direct guidance from Test Engineers, TE Managers, and Engineering Leads to support testing objectives This role offers the chance to work with cutting-edge robotic technologies and contribute to the development of new processes within a leading global company. If you are passionate about quality assurance and have a knack for working with innovative technologies, we'd like to hear from you. ABOUT AKRAYA Akraya is an award-winning IT staffing firm consistently recognized for our commitment to excellence and a thriving work environment. Most recently, we were recognized Inc's Best Workplaces 2024 and Silicon Valley's Best Places to Work by the San Francisco Business Journal (2024) and Glassdoor's Best Places to Work (2023 & 2022)! Industry Leaders in IT Staffing As staffing solutions providers for Fortune 100 companies, Akraya's industry recognitions solidify our leadership position in the IT staffing space. We don't just connect you with great jobs, we connect you with a workplace that inspires! Join Akraya Today! Let us lead you to your dream career and experience the Akraya difference. Browse our open positions and join our team!

Job Title: Receiving Inspector Shift 1st Shift: 8:30 AM - 5:00 PM 2nd Shift: 12:30 PM - 9:00 PM Days: Monday - Friday Pay Rate: $19.10/hour Employment Type: Temp-to-Perm Job Summary The Receiving Inspector is responsible for inspecting incoming and returned medical devices to ensure they meet quality, regulatory, and documentation standards. This role includes verifying sterility, temperature conditions, labeling, and required paperwork before products are placed into inventory. The position requires accurate data entry to track inspection status and working in a regulated warehouse environment. SAP and WMS Manhattan systems training provided. Candidates must be able to lift up to 40 lbs and pass a background check and drug screening (including marijuana). Department Openings Returns Department - 2 Openings Process and inspect returned products only Perform accurate data entry and system documentation Use pallet jacks as needed (experience preferred; training provided) Maintain strong attention to detail and organization Complaints Department - 1 Opening Inspect used medical devices returned from hospital surgery departments Comfort with handling open/used products, including exposure to blood, is highly desirable Must be comfortable working around blood Prepare and send clear, professional written communications regarding inspection findings What You'll Need High school diploma or equivalent experience Good computer skills and data entry Strong attention to detail and organizational skills Good written and verbal communication skills Ability to lift up to 40 lbs Previous experience in inspection, quality control, or a regulated environment is a plus Pay Details: $19.10 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for Employers San Francisco Fair Chance Ordinance Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

**Fall 2026 Co-Op - MES and Quality - Burlington, MA** As a **Fall 2026 Co-Op - MES and Quality Co-Op** ** ** in **Burlington, MA** at Keurig Dr Pepper (KDP), you will be a part of the beverage revolution. You will be working in a fast-paced, highly technical manufacturing environment that produces some of KDP's most popular beverages. Each co-op will lead high-impact projects and will be provided with opportunities to grow professionally. Come learn what it takes to succeed at an industry-leading company and help contribute to our ongoing success. You will be able to directly participate in the implementation of new technology that improves our manufacturing process. **Shift/Schedule:** + The KDP 2026 Fall Co-op Program will run from July 13 - Decemeber 11, 2026 + Full-time; 40 hours per week + Monday-Friday + 8:00am until 5:00pm + In-Person **As a Co-op you will:** + Gain knowledge in executing operational plans and projects, including data analytics and developing visualizations for DMS (Daily Management Systems) and QMS(Quality Management Systems). + Participate in AGILE project management and lead the development, verification, and testing of Data Analytics dashboards and visualization tools. + Influence software capabilities to achieve six sigma quality performance and enhance Quality Management System. + Assist with TPM (Total Productive Maintenance) implementation and Lean activities, including participation in Continuous Improvement or Kaizen events. + Test and verify new technology systems implemented for the Quality management and Manufacturing process. **Elements of the KDP Co-op Program include:** + Engaging and partnering on innovative projects to gain experience in a challenging, cross functional team environment + Participate in meet & greets and lunch & learns with KDP executives and other organization leaders + Receive professional development training such as networking, professional skills development and presenting + Be paired with a mentor to enhance your knowledge of other parts of the business and build your network + Complete a project from start to finish and present it and your takeaways to your team, department vice president and other KDP stakeholders **Total Rewards:** + $31/hour + Paid bi-weekly + $5,000 Sign-on Bonus, paid within first 30 days of employment **Requirements:** + Must be an undergraduate currently enrolled in a full-time academic program from an accredited college or university, majoring in Information Technology, Computer Science, Analytics, Engineering or another related field + Available to work 40 hours per week (M-F, 8am-5pm) + Excellent organizational skills and attention to detail with a demonstrated ability to manage multiple projects, prioritize requests, and meet deadlines + Strong communication skills including excellent listening, written, and verbal abilities + Ability to work cross-functionally, be independently driven, and a self-starter + Strong skills in Microsoft Excel and PowerPoint **Please note:** You must be work authorized in the United States on a full time basis without the need for employer sponsorship now or in the future. The Company cannot offer employment to F-1 (student) visa holders who require employer sponsorship in the future or cannot work now on a full time basis. We incorporate HireVue, an automated interview tool, into our campus recruitment process. Please visit this link (************************************************** to learn more about HireVue and how to prepare. *We recommend checking with your campus career center for additional preparation resources such as InterviewStream, Big Interview and more **Company Overview:** Keurig Dr Pepper (NASDAQ: KDP) is a leading beverage company in North America, with a portfolio of more than 125 owned, licensed and partners brands and powerful distribution capabilities to provide a beverage for every need, anytime, anywhere. We operate with a differentiated business model and world-class brand portfolio, powered by a talented and engaged team that is anchored in our values. We work with big, exciting beverage brands and the #1 single-serve coffee brewing system in North America at KDP, and we have fun doing it! Together, we have built a leading beverage company in North America offering hot and cold beverages together at scale. Whatever your area of expertise, at KDP you can be a part of a team that's proud of its brands, partnerships, innovation, and growth. Will you join us? We strive to be an employer of choice, providing a culture and opportunities that empower our team of ~29,000 employees to grow and develop. We offer robust benefits to support your health and wellness as well as your personal and financial well-being. We also provide employee programs designed to enhance your professional growth and development, while ensuring you feel valued, inspired and appreciated at work. Keurig Dr Pepper is an equal opportunity employer and recruits qualified applicants and advances in employment its employees without regard to race, color, religion, gender, sexual orientation, gender identity, gender expression, age, disability or association with a person with a disability, medical condition, genetic information, ethnic or national origin, marital status, veteran status, or any other status protected by law. **A.I. Disclosure:** KDP uses artificial intelligence to assist with initial resume screening and candidate matching. This technology helps us efficiently identify candidates whose qualifications align with our open roles. If you prefer not to have your application processed using artificial intelligence, you may opt out by emailing your resume and qualifications directly to **************** . Keurig Dr Pepper is an equal opportunity employer and affirmatively seeks diversity in its workforce. Keurig Dr Pepper recruits qualified applicants and advances in employment its employees without regard to race, color, religion, gender, sexual orientation, gender identity, gender expression, age, disability or association with a person with a disability, medical condition, genetic information, ethnic or national origin, marital status, veteran status, or any other status protected by law.

Job Description About Us Stellar Industries is a rapidly growing industry leader in manufacturing metalized ceramics. We are a major supplier of innovative, high-quality parts to the Aerospace, Photonics, Telecommunications, and Commercial industries. The company was acquired by TRUMPF Photonics in 2019 and has significant growth goals. About the Role The Quality Control Inspector Level II maintains quality standards by inspecting incoming materials from outside suppliers, in-process production, and finished products in accordance with the quality standards and operating procedures set forth by the Head of Quality Control/Quality Assurance. What You Get to Do Works independently with minimal supervision. Maintain an organized and clean work area. Uses Hand tools, including but not limited to tweezers, calipers, and micrometers. Confirms specifications by conducting visual and measurement tests. Works with a variety of blueprints and technical drawings; must be able to interpret changing requirements as products and builds vary. Completes a General Inspection Report by documenting inspection findings regarding product dimensions, quantity of parts accepted/rejected, and basis of rejection. Uses Vision Systems and documents results into the computer. Follow all safety protocols. Cross-train as requested in other areas of the company. About You Minimum of 3 years of quality control experience. Must be able to work in a sitting position for up to 10 hours. Must be able to wear a lab coat, spittle mask, and gloves while working. The position requires working with measuring devices and microscopes. Individuals must have previous experience working in a similar environment. Must be able to work independently and demonstrate extremely high levels of precision and accuracy. line, High-Temperature BTU Furnaces, as well as various facility-related items, including air handlers, air compressors, air filtration units, etc. What We Offer Competitive pay A generous benefits package that includes medical, dental, 401K plan, and PTO Employer-paid vision plan, Employer paid Basic Life and AD&D Insurance, and Employer Paid Disability Insurance Tuition Reimbursement 4-Day workweek, Monday-Thursday 12 pm-10:30 pm Monday-Thursday 12:00 pm - 10:30 pm

Job Description Busek Co. Inc. (************** research, develops, and produces spacecraft subsystem technologies for space missions. Our talented staff possess expertise in in-space propulsion, space-borne sensors, materials science, manufacturing, and high-fidelity electronic design for challenging space missions. Busek is recognized in the spacecraft on-orbit propulsion community for numerous achievements, including developing the first U.S. Hall Effect Thruster in space. Our efforts span research, development, and manufacturing of aerospace systems, with low-volume production of high-reliability in-space components and subsystems. Our facilities include over 30,000 sq. ft. of R&D labs and more than 40 vacuum chambers. Founded in 1985, Busek is located in Natick, MA, approximately 20 miles west of Boston. For more information, visit ************** Summary: As a Quality Assurance (QA) Inspector - Receiving, you will play a critical role in ensuring the quality of incoming and in-process parts and components. You will work closely with design and test engineers, manufacturing staff, and fabrication technicians (both internal and external) to verify compliance with Busek's documentation and customer requirements. This role provides a direct contribution to spaceflight programs, including groundbreaking NASA, commercial space, and defense missions. How you will make an impact: Conduct inspections of incoming and in-process components per documentation requirements. Interpret engineering blueprints, specifications, and drawings. Operate and utilize various inspection tools and gauges to verify part quality. Maintain accurate inspection records and documentation. Adhere to GD&T (Geometric Dimensioning and Tolerancing) principles and processes. Coordinate inspection efforts with coworkers to ensure workflow efficiency and quality compliance. Desired Skills: Prior experience in a technical QA parts inspection role. Previous work experience in quality control or related field. Proficiency in Microsoft Office Suite (Word, Excel). Knowledge of AS9100 or ISO 9001 standards is a plus. Experience working with small precision components. The expected salary range for this position is $52,000 - $79,000. Actual compensation will be determined by the candidate's experience, education, and alignment with organizational needs. Additional Information: To conform to U.S. Government regulations, applicants must be a U.S. citizen, lawful permanent resident of the U.S., or a protected individual as defined by 8 U.S.C. 1324b(a)(3). Benefits: Competitive Salary SEP Retirement Savings Performance Bonuses Medical, Dental, and Vision Insurance Life Insurance Long-Term / Short-Term Disability Coverage Paid Vacation, Sick Leave, and Holidays Education Assistance To comply with U.S. Government space technology export regulations, including the International Traffic in Arms Regulations (ITAR), employment at Busek requires that applicants be one of the following: A U.S. citizen A lawful U.S. permanent resident (i.e., current Green Card holder) A refugee or an individual granted asylum in the U.S. Or be eligible to receive the required authorizations from the U.S. Department of State and/or the U.S. Department of Commerce, as applicable For more information about ITAR regulations, visit this resource. Article - DDTC Public Portal Powered by JazzHR 7u9ZsAqfCq

We are seeking a Quality Control Inspector with experience in conducting first article inspection processes to ensure the quality of finished products. The ideal candidate will have some prior experience with FAI, knowledge of quality assurance techniques, and the ability to interpret engineering drawings and technical documents. Responsibilities: Assist in Conducting First Article inspection (AS9102) processes and document activities Interpret test results for acceptance or rejection Record test results and compile nonconforming output report Mechanical Inspection Electrical Point to Point wiring continuity testing Maintain calibration logs Qualifications: Minimum experience with first article inspection processes (Will Train) Knowledge of quality assurance techniques and functions Previous experience with calipers and micrometers Ability to read and interpret engineering drawings, specs, and other technical documents Mechanical aptitude Excellent communication skills both verbally and in writing

About the Role: This application is for a 6-month student role from July - December 2026. Resume review begins in January 2026. Biogen's Decision & Quality Analytics Innovation (DQAI) team is part of the Research Development & Medical (RDM) organization. The vision of the DQAI team is to drive data-driven insights from trusted data, and our team mission is to maximize the quality, efficiency and application of analytics across RDM Portfolio and Quality Management Systems through improved data and metrics management, optimization opportunities, identification of compliance risk, and enhanced business analytics application. Specifically, the DQAI team has four major focus areas: Data Management Advanced Analytics Business Intelligence Metrics Management (Performance Measurement) What You'll Do: Leverage modern AI assistants (Azure OpenAI / Copilot, GenAI-powered BI, etc.) to accelerate data exploration, automate repetitive tasks, and enhance insight storytelling. Analyze complex data from various sources to identify trends, gaps, risks, and opportunities. Work with senior staff to translate business questions into analytical problems and convert analytical outputs into actionable recommendations. Apply statistical and machine learning techniques to uncover root causes, patterns, and predictive indicators. Deliver concise insight summaries, written reports, and presentations that highlight implications and recommendations. Work with data engineering and governance teams to ensure data readiness and integrity for analytics. Support initiatives to accelerate insight discovery from portfolio analytics modeling. Develop and prototype data visualizations and dashboards. Participate in skill-building and capability-enhancement initiatives within the DQAI team. Example projects may include: Support development of custom-tailored strategic analytics solutions to answer complex questions from senior leadership. Pioneer new approaches for displaying data to engage stakeholders. Perform quality control functions to ensure the integrity of the team's work. Who You Are: You are a tech- and AI-forward problem solver who thrives on exploration and rapid iteration in a fun, collaborative team. You partner seamlessly with business stakeholders and our embedded AI developers to turn needs into analytics products and automation. Here are some of the core characteristics we're looking for: Strong analytical and critical thinking skills with a proven track record of turning data into strategic insights. Proficiency in data analysis tools and languages (e.g., Python, R). Experience applying advanced analytics, such as statistical modeling, clustering, or NLP, to real-world business challenges. Exceptional written and verbal communication skills, including the ability to synthesize complex findings for non-technical stakeholders. Ability to work collaboratively in a cross-functional environment and lead analytics initiatives from concept to insight delivery. To participate in the Biogen Internship or Co-op Program, students must meet the following eligibility criteria: Legal authorization to work in the U.S. At least 18 years of age prior to the scheduled start date. Be currently enrolled in an accredited community college, college, university or skills program/apprenticeship. Education Requirements Currently pursuing a Master's degree in Data Science, Statistics, Bioinformatics, Computer Science, Computational Biology, or related field Job Level: Internship Additional Information The base compensation range for this role is: $29.00-$29.00 The actual hourly wage offered will consider the candidate's current academic level and degree candidacy, inclusive of Associate, Bachelor's, Master's, JD, MD, PhD and MBA programs. It will comply with state or local minimum wage requirements specific to the job location. In addition to compensation, Biogen offers a range of benefits designed to support our educational employees, including, but not limited to: Company paid holidays Commuter benefits Employee Resource Groups participation 80 hours of sick time per calendar year Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Summary of Primary Responsibilities: The QC Incoming Inspector completes all activities required to approve raw materials for use in product manufacture. The position also performs inspection activities during in-process manufacturing. Specific Responsibilities: Perform quality line clears and in process inspections during the inspection and packing processes according to specific SOP requirements Issue lot numbers and control labels for incoming raw materials; perform inspections per internal procedures and specifications Release approved raw materials for use in manufacturing process to include completion of associated documents, notice of approval form (bin card) and relabeling of inventory Review MPS of other incoming inspectors for approval and release. Monitor and perform annual retain inspection; coordinate required retesting with QC; complete required documentation Perform OOS investigations and participate in MRB as required for rejected materials Perform as SME for the function and provide training as required to new employees, contractors and other QA personnel Perform biennial review for designated procedures and MPS as needed Documents; author and complete DCR as required Document all work activities according to Good Documentation Practices Maintain current training on all assigned procedures to include read & understood, skills development and classroom training activities as required Participate in other projects as assigned Job Complexity: The position works on assignments that are routine in nature and receives detailed instruction on all work. Supervisory Responsibilities: None Required Qualifications: Associates degree in the life science or relevant work experience 0 - 1 year of experience in a cGMP facility or previous experience in a QA/QC role within the industry; internship experience considered Experience using Microsoft Office or an ERP system Desired Experience, Knowledge, and Skills: Bachelor's degree preferred Experience working in a clean room environment Excellent communication and documentation skills The salary range provided is based on the Company's reasonable estimate of the base salary pay range for this position at the time of posting. Actual base pay is determined by several factors relevant to the position, including skills, competencies, experience, education, and geographic location. Anika also offers a discretionary bonus program for all full-time employees, comprehensive healthcare benefits, health savings account, 401(k) plan with up to 5% company match which includes immediate vesting, employee stock purchase plan at a 15% discount, accrued paid time off, additional long-term incentives including stock awards, and much more. At Anika, we take pride in offering robust Total Rewards, inclusive of market-leading benefits to meet our employees where they are in their career and in life. The compensation and benefits information is provided as of the date of this posting. Anika reserves the right to modify compensation and benefits at any time, subject to applicable law.

The Panther Group is seeking a Quality Inspector to support inspection activities throughout the production assembly process, from in-process inspection through final system assembly. This role is open to both entry-level and experienced candidates, with training provided for those new to quality inspection. 1st shift (for Quality Inspector 1) Mon-Fri, 6am-2:30pm. 2nd shift (for Quality Inspector 2) Mon-Fri, 2:30pm-10:30pm. or 3:30pm - midnight. Essential Duties & Responsibilities Perform in-process, first article, and final inspections throughout manufacturing Verify products meet workmanship, process, documentation, and customer requirements Follow ESD and board handling requirements Handle Moisture Sensitive Devices (MSD) per component MSL requirements Review documentation for compliance with internal procedures Disposition assemblies for rework or repair as needed Authorize shipment of product that meets industry and customer specifications Use inspection tools such as calipers, rulers, microscopes, and gauges Support ISO Quality Management Systems and site 6S objectives Accurately record inspection results in the electronic manufacturing system Support one or multiple product lines based on experience level Perform other related duties as assigned Qualifications Required: High School Diploma or GED Pass IPC-DVD-64C Component Identification. Pass IPC-A-610 Modules, 1, 2, 3, 4, 5, 6, 7 & 8. Ability to read assembly drawings, blueprints, and Bills of Materials Familiarity with First Piece, In-Process, Audit, and Final Inspection Knowledge of ESD and electronic assembly environments Ability to use Inspection Gauge (Calipers, Rulers, Microscope, etc.) Ability to use electronic manufacturing system (OCuity) Ability to use Microsoft Office tools like Excel and Word as well as shop floor control systems (Aegis). Ability to work in a team-oriented manufacturing environment Strong attention to detail and sense of urgency Comfortable performing repetitive inspection tasks Ability to follow written procedures and instructions Preferred (training may be provided): IPC-A-610 and IPC-DVD-64C certifications Experience Levels Entry-Level: 0-6 months manufacturing or inspection experience Experienced: 2+ years of quality inspection or related technical experience Technical or vocational certification may substitute for experience Pay is $20 - $28 / hour depending on experience and shift. #INDENG #ZR

Summary: The Lead Housing Quality Standard (HQS) Inspector is responsible for conducting any mandatory inspection for all leased units under the Rental Assistance Program in accordance to the Department of Housing and Urban Development (HUD) and Department of Housing and Community Development (DHCD) program guidance. As the Lead HQS Inspector the incumbent is expected to assist the Inspections' Supervisor in providing training to newly hired inspectors and with administrative duties as assigned. Why Work for SMOC? Paid Time Off: All full-time employees can accrue up to 3 weeks of vacation, and 2 weeks of sick time and are eligible for 12 paid holidays during their first year of employment. Employer-paid Life Insurance & AD&D and Long-Term Disability for full-time employees. Comprehensive Benefits Package including Medical Plans through Mass General Brigham with an HRA Employer cost-sharing program, Dental Plans with Orthodontic Coverage, and EyeMed Vision Insurance available to full-time employees. 403(B) Retirement Plan with a company match starting on day one for all full-time and part-time employees. Additional voluntary benefits including; Term and Whole Life Insurance, Accident Insurance, Critical Illness, Hospital indemnity, and Short-Term Disability. Flexible Spending Accounts, Dependent Care Accounts, Employee Assistance Program, Tuition Reimbursement and more. Primary Responsibilities: Conduct thorough HUD/DHCD HQS inspections of all SMOC RAPS existing units, potential new units, and the reinspection of those units as required including physical and remote virtual inspections. Verify unit compliance based on health and safety requirements. Verify unit conditions for rent reasonableness comparisons. Enter all inspection data into the MRI Tenmast Software Systems' Inspection module and monitoring information as needed; printing all required inspection-related letters for participating tenants and owners. Assist the Inspection Supervisor in providing "on the job" training for newly hired HQS inspectors in the field Assist the Inspection Supervisor in monitoring the various types of inspections conducted by the HQS Inspection team including remote virtual inspections, re-inspections, inspections conducted using an owner self certification and physical inspections Make recommendations to the Inspection Supervisor on behalf of the HQS inspectors on process and procedure Monitor HQS supplies and make requests to the Program Director on orders for necessary equipment such as gloves, shoe coverings and personal protective equipment as needed Utilize and maintain inspection-related equipment on a regular basis, including camera, hand-held inspection devices or tablets, flashlight, cell phone, tick tester, and inspection-supply cache. Engage all clients by understanding and addressing their needs whether within or outside the scope of work. Attend & participate in engagement team meetings as requested and communicate effectively with clients and staff in other areas. Maintain confidentiality of client, employee and agency information in accordance with federal and state laws and funder requirements. Ensure compliance with program/department, agency and/or funder requirements, as well as SMOC policies & procedures. Other duties as assigned. Knowledge and Skill Requirements: Education: High school diploma or equivalent Minimum years of related experience: 1-2 years preferred Knowledge of Excel, Windows, Word and PCs, ability to work well in a very high volume and productivity environment, ability to handle potentially stressful situations and sensitivity to the needs of economically- disadvantaged clientele. Valid Mass. driver's license and insurance Mobility to use office machines, sitting, standing, ability to lift archive boxes filled with files. Must meet all required DHCD program certifications within 1 year. Organizational Relationship: Directly reports to HQS Inspection Supervisor. Indirectly reports to Program Director, Assistant Director and Division Director. Direct reports of this position are none. Indirect reports of this position are HQS Inspectors. Physical Requirement: Physical effort required to do the job: Mobility to use office machines, sitting, standing, ability to lift archive boxes filled with files. Working Conditions: This job requires working in many different conditions and places. About 80% of the time is outside the office either on the road or at a tenant's unit. Therefore, conditions range from an office environment to an outdoor environment that can be dirty, wet, cold, hot, difficult and risky. As part of the responsibilities of this position, the Lead Inspector will have direct or incidental contact with clients served by SMOC in various programs funded or administered through the Executive Office of Health and Human Services. A successful background check is required.

We are a growing manufacturing company looking for an individual to assist or lead our quality control department Requirements A qualified individual would: Be able to read and interpret drawings. Understand GD&T. Understand a variety of sampling plans. Utilize best practice inspection methods to ensure product conforms to customer and drawing specifications. Be familiar with and able to use a variety of inspection tooling (micrometers, calipers, CMM, indicators, optical comparator, etc). Have good computer skills (Microsoft Office, Outlook, be able to learn a robust ERP system). Be familiar with completing first article inspections per AS9102 and complete utilizing specialized software. Have a good organizational skill set as each customer has a different set of requirements that are critical to product acceptance. Be familiar with the requirements of ISO9001. Attention to detail is critical. FULL TIME EMPLOYEE BENEFITS: Competitive compensation based on experience BCBS Medical, Altus Dental and Vision, Disability and Life Insurance - 100% Company Paid. Paid personal and vacation time (PTO) 10+ Paid holidays 401K plan Potential for Growth OT based on business conditions COMPANY: Bendon Gear is a precision machine and gear company doing business for over 40 years, with a stable set of excellent customers. We are a good, solid company, and we wish to build a team of good people who are motivated, flexible, and capable. Job Types: Full-time, Part-time Salary: $18.00 - $27.00 per hour Benefits: 401(k) Dental insurance Health insurance Life insurance Paid time off Professional development assistance Vision insurance Schedule: 10 hour shift 8 hour shift Monday to Friday Salary Description $18 - 27.00 / Hr

Rennscot MFG, founded in 2017, started as a motorsports-focused shop in the aftermarket automotive industry. Now, they are a leading provider of advanced manufacturing services located in Woburn, MA. Rennscot MFG strives to be more than just a machine shop; they solve problems in innovative ways, using a suite of integrated services to fuel a passion for ideation. With a focus on diversifying into commercial and critical technology sectors, Rennscot MFG delivers cutting-edge technologies and unwavering commitment to quality. They offer a comprehensive range of services, including reverse engineering, metal & polymer additive manufacturing, and precision machining to support various industries' needs. For more information, visit rennscotmfg.com. Description The Quality Control Inspector is responsible for ensuring that manufactured components meet engineering and customer specifications through precise inspection processes. This role places a strong emphasis on visual inspections, along with manual inspection methods, and requires a keen understanding of technical drawings and GD&T. Candidates will be considered for either an L1 (entry-level) or L2 (experienced) inspector position based on experience and qualifications. Responsibilities Operate pre-programmed CMM inspections (Zeiss/Calypso preferred) Load/unload parts and verify setups Interpret CMM results and compare them against engineering requirements Document findings in the MES (ProShop) and communicate deviations Perform manual inspections using a variety of precision metrology tools Calipers, micrometers, height gauges, thread gauges, bore gauges, etc. Visual inspections for defects such as nicks, scratches, and finish inconsistencies Review technical drawings and apply GD&T principles to inspections Conduct receiving, in-process, and final inspections Assist in non-conformance investigations, root cause analysis, and corrective actions Maintain accurate inspection records and ensure compliance with AS9100/ISO9001 standards Collaborate with machinists, engineers, and quality team members to resolve inspection-related concerns Adhere to company safety protocols, including proper PPE usage (eye protection, hearing protection, etc.) Step into other support roles as needed based on company demands; assist with CNC machine operation, post-processing additively manufactured parts, mechanical assembly, or logistics tasks (e.g., driving components to/from outside processing vendors) Required Skills & Qualifications Experience in quality inspection within a manufacturing environment Strong ability to interpret technical drawings, GD&T, and work instructions Proficiency in basic metrology tools (calipers, micrometers, etc.) Familiarity with non-conformance documentation and quality reporting Attention to detail and ability to work independently in a fast-paced environment Preferred Skills & Qualifications Experience running CMM programs (Zeiss/Calypso preferred) Ability to make minor adjustments to Calypso programs Understanding of statistical process control (SPC) and quality tools (FMEA, control plans, etc.) Experience working in regulated industries (aerospace, medical, automotive, etc.) Physical Demands Standing for extended periods Lifting/moving objects up to 50 lbs Fine motor skills for handling small precision components Working in an industrial environment requiring PPE (eye protection, hearing protection, etc.) ITAR Requirement To conform to US Government export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a US citizen, lawful permanent resident of the US, protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the US Department of State. Learn more about the ITAR here: **************************************************************************************** Rennscot MFG is an Equal Opportunity Employer; employment with Rennscot MFG is governed on the basis of merit, competence and qualifications and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability or any other legally protected status.

The Quality Control Technician - Troubleshooting is responsible for inspecting and testing cable and wire products and processes to ensure they meet all quality standards, specifications, and regulations. This includes performing visual inspections, dimensional measurements, electrical, and functional tests. The primary function of this role is to evaluate nonconforming products and to determine the necessary actions to rework the product. The QC Technician must also be able to read and interpret blueprints, engineering drawings, and specifications. This position requires the use of High Voltage, all safety guidelines, procedures, and regulations to prevent accidents and ensure a safe working environment must be followed. The Quality Control Technician - Troubleshooting is a respectful team-player that works well with diverse internal team members. This position is ambitious, self-motivated, results-driven, and demonstrates problem solving skills with sound judgment. This role is also responsive, flexible, accessible, detail oriented, willing to embrace change and proactively adjust plans. Partnering with and elevating others by communicating with peers to increase awareness and ensure team success. Essential Duties and Responsibilities: Troubleshoot nonconforming cables, fill out nonconformance reports and communicates findings to Production Quality Supervisor and Quality Manager Detect and report unusual or non-conforming documentation, materials, conditions, or product to Production Quality Supervisor and Quality Manager. Assist and sometimes lead Root Cause and Corrective Action efforts. Inspect materials, components, and final product to ensure they meet quality standards. Measure dimensions of cable and wire products to ensure they meet specifications. Conduct visual and electrical tests on cable and wire products to ensure they meet performance requirements and identify any defects. When required, perform functional tests on cable and wire products to ensure they operate as designed. Document the results of all tests and inspections. Create, update, compile, save and maintain documentation into internal database. Work with various internal personnel and departments to communicate and resolve quality issues. Comply and support company policies and quality management system. Maintain and create a clean, uncluttered environment that reduces waste and optimizes productivity by following the 5S steps: sort, set in order, shine, standardize, and sustain. When required, help with continuous improvement efforts. More additional responsibilities may be applicable per the Quality Manager. Qualifications: High school diploma or equivalent. 1+ year of experience in quality control, preferably in the cable and wire manufacturing industry. Experience with visual inspection and dimensional measurement. Basic understanding of Microsoft Office and Adobe. Ability to read and interpret blueprints, engineering drawings, and specifications. Strong attention to detail. Ability to work independently and as part of a team. Strong communication skills. Proficient with computers and comfortable using Microsoft Office Suite (Word, Excel, etc.). Physical Qualifications: The physical demands described are representative of those that must be met by an employee to successfully perform the essential function of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly required to sit; stand; crouch; stoop; walk; talk; hear; use hands to handle or feel assemblies; reach with hands and arms for materials and tools. The employee must occasionally lift and/or move up to twenty-five (25) pounds. They must also have the ability to see details at close range (within a few feet of the observer), color vision, depth perception and ability to focus. This position requires use of information or access to hardware and documents which are subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee, or Refugee. Benefit Conditions: Waiting period may apply Only full-time employees are eligible This Job Is: A job for which military experienced candidates are encouraged to apply Job Type: Full-time Salary: $20.00 - $25.00 per hour Benefits: 401(k) Dental insurance Health insurance Paid time off Vision insurance Experience level: 1 year Schedule: 8 hour shift Day shift Monday to Friday Overtime Work setting: In-person Experience: Blueprint reading: 1 year (Required) Quality control: 2 years (Preferred) Work Location: In person

Wave Life Sciences is a biotechnology company focused on unlocking the broad potential of RNA medicines to transform human health. Our RNA medicines platform, PRISM, combines multiple modalities, chemistry innovation and deep insights in human genetics to deliver scientific breakthroughs that treat both rare and prevalent disorders. Our toolkit of RNA-targeting modalities includes editing, splicing, RNA interference and antisense silencing, providing us with unmatched capabilities for designing and sustainably delivering candidates that optimally address disease biology. Our diversified pipeline includes clinical programs in Duchenne muscular dystrophy, Alpha-1 antitrypsin deficiency and Huntington's disease, as well as a clinical program in obesity and a preclinical program in NASH/MASH. Driven by the calling to “Reimagine Possible”, we are leading the charge toward a world in which human potential is no longer hindered by the burden of disease. Description: Wave Life Sciences seeks a highly motivated and energetic chemistry, biochemistry, or chemical engineering major to join its Analytical/QC team in Lexington, Massachusetts. The co-op role will be responsible for routine testing and method development activities in support of process development, GMP production and clinical development. The position offers the opportunity to directly learn analytical methods and techniques that are in widespread use throughout the pharmaceutical and biotech industry. In addition, the co-op student will gain exposure to important functions of the development and manufacturing of pharmaceuticals, including analytics and stability, manufacturing processes and quality systems. A successful candidate will have hands-on experience with basic wet chemistry, sampling and testing organic or inorganic compounds, as well as other laboratory techniques. Experience with some of the following are a plus: HPLC, Karl Fischer moisture analysis, UV-Vis spectroscopy, microbiology testing, FTIR spectroscopy, chemical synthesis or purification processes. The candidate should also be able to adapt to a fast pace dynamic environment where priorities can change rapidly. This position is based in Lexington, MA at Wave's growing GMP manufacturing facility. Responsibilities: Perform analytical testing of in-process, finished product (API), raw materials Analyzes research and production samples Documentation and organization of data sets and reporting of results to other departments Troubleshoots analyses and assists in performance of investigations Assists in procurement and tracking of reagents and materials Reviews data generated by other analysts Executes method qualifications and validations Minimum Qualifications: Working towards a Bachelor's degree in chemistry or a related discipline (i.e. biochemistry, chemical engineering) At least two years of an undergraduate education completed within a related discipline. Intern must have successfully completed chemistry courses. Must possess excellent oral and written skills, as well as superior organizational skills. Analytical chemistry laboratory skills Analytical chemistry knowledge Competencies: Effective Communication Independence Flexibility/Adaptability to Change Accountability Teamwork Decision making EEO Statement: Wave Life Sciences provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, Wave Life Sciences complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Wave Life Sciences expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. Improper interference with the ability of Wave Life Sciences' employees to perform their job duties may result in discipline up to and including discharge. We value our relationships with professional recruitment firms. To protect the interests of all parties and given the large volume of inquiries received from third-party placement agencies, we are not able to respond to all agency inquiries. We do not accept unsolicited resumes from any source other than directly from candidates for current or future positions. Submission of unsolicited resumes in advance of a signed agreement between our company and a placement agency does not create an implied obligation and, if an unsolicited candidate represented by a placement agency is hired, we are not obligated to pay a fee. Only approved recruitment firms will be allowed to provide services to Wave Life Sciences, USA.

Full-time Description Department: Quality Supervisor: Quality Assurance Manager Hourly Rate Range: Hourly rate will be commensurate with experience Schedule: M-F, 40 hours/ week- OT as required Education Requirements: High School Diploma or GED Years of Experience: 3 years related experience Position Summary: Quality technician I will perform inspections, tests, and measurements to ensure that products consistently meet both internal and external quality standards throughout the production process. Your attention to detail and strict adherence to procedures will support continuous improvement in manufacturing operations. You will collaborate closely with the production team to ensure all outputs meet company and industry standards, while contributing to our ISO?9001 and AS9100 certification compliance efforts. Key Responsibilities: · Conduct visual, dimensional, and functional inspections on raw materials, in-process components, and finished products according to established protocols. · Use precision measurement tools (e.g., calipers, micrometers, gauges) and equipment (e.g., CMM) to verify product specifications. · Perform routine sampling, testing, and record results in the quality management system (QMS). · Identify non-conforming items, quarantine defects, and initiate corrective actions in collaboration with production teams. · Assist in root cause analysis, corrective/preventive action (CAPA) investigations, and implement improvements. · Maintain calibration schedules and ensure inspection equipment is in good operating condition. · Generate quality reports and provide feedback to production and engineering teams. Requirements Qualifications: · High school diploma or equivalent; Associate degree or technical certification in quality assurance, manufacturing, or related field preferred. · 1-3 years of experience in quality control or inspection, preferably in manufacturing engineering, process improvement, or industrial engineering. · Proficient with precision measurement instruments and quality inspection tools. · Working knowledge of statistical process control (SPC) and root cause analysis methods. · Familiarity with quality management systems ISO 9001 / AS9100. · Knowledge of root cause analysis techniques (5 Whys, Fishbone, FMEA). · Strong background in lean manufacturing, Six Sigma, and continuous improvement methodologies. · Strong attention to detail and problem-solving abilities. · Effective verbal and written communication skills. · Ability to work independently and collaboratively in a fast-paced environment. · Basic computer skills; experience with QMS software and MS Office. Preferred Qualifications: · Certified Quality Inspector (CQI) or ASQ certification. · GxP/GMP training. · Six Sigma Green Belt (Or Above) Key Performance Indicators (KPIs) 1. First Pass Yield - Percentage of products that pass quality inspection without rework. 2. Inspection Coverage: - Percentage of products/components inspected according to defined sampling plan. 3. Measurement Accuracy - Percentage of measurements and tests recorded correctly in the QMS. 4. Procedure Adherence Rate - Percentage of inspections performed according to standard operating procedures (SOPs). 5. Data Accuracy - Accuracy of recorded inspection and testing data in QMS. Benefits: 401(k) 401(k) matching Dental insurance Flexible spending account Health insurance Life insurance Paid time off Professional development assistance ITAR COMPLIANCE This position requires access to or use of information which is subject to the federal International Traffic in Arms Regulations (ITAR). All applicants for this position must be U.S. Persons within the meaning of ITAR. ITAR defines "U.S. Person" as U.S. citizen, lawful permanent resident of the U.S., person admitted as a refugee to the U.S., person granted asylum in the U.S., or person granted the status of alien lawfully admitted for temporary residence to the U.S. under 8 U.S.C. §1160(a) (for special agricultural workers) or 8 U.S.C. §1255(a)(1) (an amnesty program).

The QC inspector is responsible for ensuring that all products meet quality standards. This includes inspecting raw materials used in the production process, conducting tests on finished products and performing audits to identify potential areas of improvement. The QC inspector must be knowledgeable of the relevant safety regulations and have excellent attention to detail and problem-solving skills. Essential Functions Responsible for individual Inspection activities Undergo training when necessary Adhere to policies and procedures related to specific customer requirements Ability to understand specific directions and follow guidelines that are common throughout the department Ability to maintain a constant focus on quality and accuracy Ability to work with minimal supervision Specific competencies include but are not limited to following the Gowning, Personal Hygiene Procedures, and all other QC Inspection Work Instructions and SOPs including formatting Excel if required, Use of inspection equipment (Bench Linc, Vision Systems, Tensile Tester, Pin Gages, Ring Gages, Calipers, rulers, and Customer supplied fixtures) Perform Visual Inspection (using Tappi Chart) and Feel Testing. Operating the Annealing Ovens Obey all safety rules, use caution in work activities, and continuously practice safe behaviors Immediately report unsafe conditions/behaviors and work-related injuries to site supervision Qualifications Preferred High school diploma or equivalent 1 year of Product Operator experience necessary Experience within the department must be gained within 90 days for use of specific measuring equipment, displaying an understanding of the job requirements and any devices required to complete inspection/test activities Understand Quality Management System (QMS) requirements Training on the specific equipment must be fully completed within 90 days of hire Equivalent combination of education and experience is preferred An Affirmative Action / Equal Opportunity Employer Proterial Cable America, Inc. provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. As a Federal Contractor, we encourage priority referral of protected veterans under VEVRAA.

Summary of Primary Responsibilities: The QC Incoming Inspector completes all activities required to approve raw materials for use in product manufacture. The position also performs inspection activities during in-process manufacturing. Specific Responsibilities: Perform quality line clears and in process inspections during the inspection and packing processes according to specific SOP requirements Issue lot numbers and control labels for incoming raw materials; perform inspections per internal procedures and specifications Release approved raw materials for use in manufacturing process to include completion of associated documents, notice of approval form (bin card) and relabeling of inventory Review MPS of other incoming inspectors for approval and release. Monitor and perform annual retain inspection; coordinate required retesting with QC; complete required documentation Perform OOS investigations and participate in MRB as required for rejected materials Perform as SME for the function and provide training as required to new employees, contractors and other QA personnel Perform biennial review for designated procedures and MPS as needed Documents; author and complete DCR as required Document all work activities according to Good Documentation Practices Maintain current training on all assigned procedures to include read & understood, skills development and classroom training activities as required Participate in other projects as assigned Job Complexity: The position works on assignments that are routine in nature and receives detailed instruction on all work. Supervisory Responsibilities: None Required Qualifications: Associates degree in the life science or relevant work experience 0 - 1 year of experience in a cGMP facility or previous experience in a QA/QC role within the industry; internship experience considered Experience using Microsoft Office or an ERP system Desired Experience, Knowledge, and Skills: Bachelor's degree preferred Experience working in a clean room environment Excellent communication and documentation skills The salary range provided is based on the Company's reasonable estimate of the base salary pay range for this position at the time of posting. Actual base pay is determined by several factors relevant to the position, including skills, competencies, experience, education, and geographic location. Anika also offers a discretionary bonus program for all full-time employees, comprehensive healthcare benefits, health savings account, 401(k) plan with up to 5% company match which includes immediate vesting, employee stock purchase plan at a 15% discount, accrued paid time off, additional long-term incentives including stock awards, and much more. At Anika, we take pride in offering robust Total Rewards, inclusive of market-leading benefits to meet our employees where they are in their career and in life. The compensation and benefits information is provided as of the date of this posting. Anika reserves the right to modify compensation and benefits at any time, subject to applicable law.