Quality Control Inspector Jobs in Gardner, MA

Title: Mechanical Inspector (2nd shift) Duration : Long term contract Mechanical Inspector is responsible for ensuring that manufactured parts and assemblies meet specified standards and tolerances. Using tools like CMM and understanding GD&T principles are critical aspects of this role. Key Responsibilities Inspection Tasks: Use CMM to perform precise measurements of parts and assemblies. Verify dimensions, tolerances, and geometric features per engineering drawings. Understanding GD&T: Interpret engineering drawings and specifications with GD&T annotations. Verify form, orientation, location, and runout tolerances on parts. Documentation: Record and document inspection results in reports. Provide feedback to production teams on detected deviations. Collaboration: Work with design, engineering, and production teams to resolve quality issues. Assist in troubleshooting problems related to machining and assembly processes. Equipment Management: Calibrate, maintain, and operate precision inspection equipment, including CMMs and manual tools like calipers, micrometers, and height gauges. Skills and Qualifications Technical Knowledge: Proficient in GD&T (ASME Y14.5) and experience with CMM programming (e.g., PC-DMIS, Calypso). Measurement Tools: Familiarity with both automated (CMM) and manual inspection tools. Detail-Oriented: Exceptional attention to detail for verifying high-precision parts. Software Proficiency: Experience with CAD/CAM software and interpreting 3D models. Communication Skills: Ability to document and communicate inspection findings effectively. Thanks Ritika Aithmian Lead Recruiter **********************************

Our client, a leading manufacturer of paper products, is seeking a Quality Control Technician to join their team in North Andover, MA. This direct hire position offers competitive pay and benefits. In this role, you will become an expert in the operation of production machines, perform daily Quality Control functions, and develop Manufacturing Technician skills to support R&D, Production and Engineering. The ideal candidate will have a 2- or 4-year degree in Engineering (or equivalent experience), the ability to work hands-on in a fast-paced environment, organizational skills, and a keen attention to detail. If you're a self-starter looking for a dynamic opportunity, apply today! Location: NORTH ANDOVER, Massachusetts Job type: Permanent Salary: $52,000 - 64,480 per year Work hours: 8am to 4pm Education: High School Responsibilities: Learn and assist with production equipment and troubleshooting. Test products during production to Quality Test Procedures and document results. Collaborate with operators to ensure quality production. Analyze production data and maintain product specifications. Update Quality Control Test Procedures and Manufacturing Process Sheets. Minimize waste and improve productivity and quality. Investigate claims, non-conforming products, and process issues; issue Corrective Actions. Work with supply vendors on production/quality needs. Ensure quality products are produced in collaboration with management. Assist with product development and scale-up for manufacturing release. Review Safety Procedures and participate in safety meetings. Maintain Safety Training Records. Qualifications: Experience level: Experienced Minimum 2 years of experience Education: High School (required) Skills: Quality Troubleshooting MS Office #quality #qualityengineering #engineering #qualitytechnician #Troubleshooting

HRSG Inspector Employment Type: Full-Time Travel: Up to 5 days per week during Spring and Fall seasons We are seeking an HRSG Inspector to perform on-site inspections of Heat Recovery Steam Generators (HRSGs) and boilers at power plants. This role involves evaluating system performance, identifying potential issues, and providing customers with practical recommendations to enhance reliability and efficiency. The ideal candidate will have a strong technical background in heat transfer, thermodynamics, fluid mechanics, or structural engineering, along with excellent communication and reporting skills. Key Responsibilities Conduct on-site inspections of HRSGs and boilers to assess performance and identify maintenance needs. Analyze system conditions and provide technical recommendations to optimize plant operations, reliability, and efficiency. Work closely with plant personnel to understand operational challenges and propose solutions. Generate comprehensive inspection reports, summarizing findings, data, and recommended actions. Present project results and recommendations to customers clearly and professionally. Maintain compliance with industry regulations, safety procedures, and plant protocols. Travel up to 5 days weekly during peak seasons (Spring and Fall) to conduct site visits. Required Qualifications Technical proficiency in at least two of the following fields: Heat Transfer Thermodynamics Fluid Mechanics Structural Engineering Plant Operations Mechanics of Materials Strong communication skills to engage with customers and understand their operational needs. Excellent report writing and presentation skills to summarize inspection results and recommendations. Ability to travel extensively during peak seasons. Preferred Qualifications Experience in power plant operations, maintenance, or inspections. Knowledge of boiler and HRSG performance assessment methods. Familiarity with industry standards and safety regulations related to HRSG and boiler inspections. Why Join Us? This is an exciting opportunity to work in power generation and plant reliability, providing critical insights to improve efficiency and reduce downtime. We encourage you to apply if you have a strong technical background, enjoy problem-solving, and thrive in field-based roles!

Our client is seeking a dedicated and skilled Inspector to join their team. In this role, you will be responsible for performing inspections and audits of purchased parts, materials, equipment, and quality control programs to ensure compliance with company standards. You will interpret technical documentation such as manufacturing drawings, diagrams, specifications, and lists to assess whether units or systems meet quality standards. Additionally, you will conduct sampling and testing of incoming components and raw materials, ensuring that all products meet the required specifications for in-process or final assemblies. Essential Duties and Responsibilities (but not limited to): Perform a variety of inspections on materials, components, assemblies, and systems, including visual, workmanship, dimensional, and electrical inspections. Generate and revise inspection procedures and associated workflows to improve processes. Conduct source inspections at off-site facilities as required. Identify problem areas, bottlenecks, and assist in their resolution to maintain efficiency and quality. Document inspection results and generate detailed inspection reports. Ensure that work is performed in a consistent manner by developing and maintaining clear procedures. Adhere to safety and security rules and maintain good housekeeping practices in the workplace. Assist in the training and mentoring of lower-grade personnel and new hires to ensure they understand department and lab policies. Work independently with minimal supervision to complete assignments effectively and efficiently. Qualifications: High school diploma or equivalent, plus two years of technical schooling in engineering, science, and/or mathematics, or Associate's degree in engineering or science, or five college-level technical courses in engineering, science, or mathematics, or Quality Inspector Certification (CQI) from the American Society for Quality (ASQ) is also acceptable. Minimum of five years of experience in a quality assurance organization, specifically related to the inspection of mechanical and/or electronic commodities. Demonstrated working knowledge of industry and military standards associated with quality control of electronics and mechanical commodities, including soldering, welding, crimping, cross-sectional analysis, wiring, and cabling. Ability to interpret and work with engineering drawings, sketches, and inspection procedures. Proficient in Microsoft applications such as Word and Excel. Strong time management, organizational, and decision-making skills. Capable of following both verbal and written instructions accurately. Excellent attention to detail and quality control focus. IPC certifications, such as IPC-610 and IPC-600, are highly preferred. Candidates may be required to obtain a government security clearance. Candidates must be a United States Citizen. POST-OFFER BACKGROUND CHECK IS REQUIRED. Digital Prospectors is an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other characteristic protected by law. Digital Prospectors affirms the right of all individuals to equal opportunity and prohibits any form of discrimination or harassment. Make this your next career move as one of our many long-term contractors or employees! Work as our full-time employee with full benefits (Medical, Dental, Vision, Life, STD, LTD, PTO, etc.) - OR - work as a W2 hourly contractor at a higher pay rate if you don't need the benefit package. Come see why DPC has achieved: 4.9/5 Star Glassdoor rating and the only staffing company (< 1000 employees) to be voted in the national Top 10 ‘Employee's Choice - Best Places to Work' by Glassdoor. Voted ‘Best Staffing Firm to Temp/Contract For' seven times by Staffing Industry Analysts as well as a ‘Best Company to Work For' by Forbes, Fortune and Inc. magazine. As you are applying, please join us in fostering diversity, equity, and inclusion by completing the Invitation to Self-Identify form today! ******************* Job #17497

Minimum 3 years' experience conducting Source Inspections on populated CCA(s) Current IPC-610 Certification - Recently lapsed Certifications will be evaluated Experience with J-STD-001, Class 3 Industry Standard Experience with ESD Programs Experience with complex engineering drawings, specifications/standards Experience with Final Source Inspections Experience with all types of Product Certifications Completion of Customers Inspection Record Form Computer Skills Notes: Duration: 1 Year Plus First Shift: 1- 2 Visits/Month or As Required at a 4 Hour Minimum/Visit Location: Billerica, MA 01862 Travel Time / Mileage Compensation Paid on-site training at the customer's facility Local Candidates Preferred US Citizenship required; W2 contract position to work on as needed basis Start Date: Upon Customer Approval ******************

Growing Radiopharmaceutical Contract Manufacturing (CMO) site has a new direct hire opportunity for a Quality Control Specialist to join their team! The CMO site manufactures and provides radiopharmaceuticals, medical isotopes, and related services, particularly for cancer treatment and research. They offer a very generous compensation & benefits package as well as a very pleasant work culture! Job Summary: The Quality Control Specialist will assist the Quality Control Manager in maintaining an effective quality control program which consistently strives to test and release high quality products on time. This person will participate in quality tests and inspections to verify that appropriate current procedures are followed and will keep the QC Manager fully informed on the status of QC activities. Responsibilities: Operates under the guidance of the QC Manager to assure compliance with the company's quality control program as well as the quality management system (QMS) Communicates with the QC Manager on activities related to quality control Performs final quality control testing on products as assigned by the QC Manager Performs periodic calibration and qualification of analytical equipment, which include: Pipettes Analytical balances Incubators and ovens Freezers and refrigerators Gamma and alpha spectrometers Liquid scintillation counters HPLC Systems Assists in analytical methods development and validation activities Performs incoming materials inspection and carries out quantitative and qualitative tests to qualify them as per approved protocols Maintains inventory and usage log for raw materials Assists in deviations, root cause analyses, corrective/preventive actions and non-conformity reports Carries out filing, organizing and record keeping of QC documentation Recommends continual improvement changes to QC procedures and processes where necessary. Performs other duties as assigned by QC manager Requirements: Bachelor of Science (B.S.) degree in relevant discipline (Chemistry, Pharmacy, Nuclear Chemistry, Biochemistry etc.) Minimum 2 - 3 years' experience with pharmaceutical Quality Control, preferably radiopharmaceutical. Proficient in the operation, calibration and routine maintenance of general analytical equipment, such as balances, pipettes, HPLC systems etc. Proficient in the review, revision and authoring of official documents such as standard operating procedures, work instructions etc. Proficient in Microsoft Excel and Word Able to lift up to 50 lbs. Desirable Traits: Experience of working with measuring equipment pertaining to radioactivity (gamma spectrometers, alpha spectrometers, liquid scintillation analyzers, gamma counters, dose calibrators etc.) is highly desirable Experience of working with HPLC, GC, ICP/OES is highly desirable Experience working with electronic document management systems / LIMS Experience in statistical analysis and trending of QC-relevant data Knowledge of the conceptual and practical application of cGMP in a pharmaceutical environment Able to work in a fast-paced environment and meet quality, accuracy and timeliness objectives Hands-on, having a knack of working with tools and fixing minor equipment maintenance issues Detail-oriented and organized with excellent written and verbal skills Able to work independently as well as in a team Is flexible to work odd hours and occasionally on weekends/holidays, as needed.

Pay Rate: $28.50 Per Hour Schedule: 7:00am to 3:30pm Principal Responsibilities: Responsible for performing first detailed inspection of incoming or purged parts, materials, components, assemblies, equipment, and document results Coordinates the collection and disposition of purged material Determines or assists in determining methods, sequences and procedures necessary for inspection Works from written procedures, drawings, sketches and specifications Generates Engineering Change Requests to correct drawing issues noted during inspection Adapts inspection measuring devices and procedures where necessary Requirements- Mechanical Inspection experience Experience with Comparators, Height Gauges, Verniers, hand tools. Familiarity with IPC Standards

The Sterile Processing Quality Assurance Specialist (QA) is responsible for ensuring the accuracy and proper assembly of instrument trays according to pick sheets. This role includes verifying instrument placement, checking for good working order, and preparing trays for processing. The QA specialist provides immediate feedback and coaching, documents data in provided software, and identifies discrepancies/errors in count sheets. Additionally, the QA specialist may assist in developing, recommending, and implementing educational needs, internal standards, policies, and procedures to improve the quality and effectiveness of patient care and sterile processing. Participation in hospital, departmental, and multidisciplinary programs, committees, and special projects may also be required. Values Statement The Sterile Processing Quality Assurance Specialist embodies the hospital's core values in all interactions with patients, families, and colleagues. Duties Notice The following statements describe the essential duties of the person assigned to this job. They are not intended as an exhaustive list of all job duties and responsibilities. In the event of a public health emergency, you may be asked to assume additional duties in other areas of the organization if needed. Principal Duties and Responsibilities Kit Review and Accuracy: Maintains review kits for accuracy and instrument functionality. Ensures every kit is audited and entered into the database. Error Trend Identification: Identifies trends in kit errors and reports findings from SPM collation to monthly staff meetings. Immediate Feedback and Coaching: Provides immediate feedback to assemblers, offers coaching to staff when gaps arise, and recognizes staff that are unreceptive to coaching. Recommends focused needs to educators and specialty training. Staff Evaluation: Recognizes staff that are unreceptive to feedback and reports findings and trends. Case Cart Review: Reviews and inspects case carts for accuracy and completeness. Helps create a missing/priority list to complete case carts. Discrepancy Reporting: Accurately reports all discrepancies. Quality Assurance Support: Supports enterprise programs for quality assurance needs. Other Duties: Performs other duties as assigned. Certification/Registration Certification/Registration Required: SPD Certification, Level II Tech Certification/Registration Preferred: CIS Education Required Education: High School Diploma or Surgical Technologist Preferred Education: Bachelor's Degree Work Experience Required Work Experience: Certification in SPD, 5+ years of experience Preferred Work Experience: None specified Knowledge, Skills, and Abilities Analytical Skills: Ability to resolve complex problems requiring the application of clinical, scientific, or technical principles, theories, and concepts and in-depth, cross-functional, experienced-based knowledge. Communication Skills: Effectively deal with conflicting views or issues, mediate fair solutions, and possess well-developed writing skills. Interpersonal Skills: Ability to communicate effectively with supervisors, coworkers, and all levels of hospital staff, including the Operating Room and physicians. Multi-tasking: Capable of planning, organizing, and multi-tasking projects. Flexible and self-motivated. Technical Reading: Ability to read and understand applicable IFU and SPM count sheets. Customer Centric Behavior: Demonstrated customer-centric behavior. OR Workflow Knowledge: Familiarity with OR workflow, procedures, medical terminology, and instrumentation. Infection Control: Knowledge of infection control and health & safety policies and procedures. Cultural Sensitivity: Sensitivity to recognize, appreciate, and incorporate differences, diversity, and preferences into the provision of care. Software Proficiency: Thorough working knowledge of Microsoft Office applications and the capability to learn software programs.

WHO WE ARE RoslinCT is a world-leading cell and gene therapy contract development and manufacturing organization creating cutting-edge therapies that change people's lives. Collaborative, dedicated, and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilizing ground-breaking science. THE ROSLINCT WAY Here at RoslinCT, our team can contribute to the development of revolutionary treatments. We live every day by our core values: Partner Focus, One Team, Personal Growth, Integrity, Innovation, and Trust and Respect. We put our employees at the forefront by providing a flexible and empowering work environment, an attractive benefits package, and an emphasis on work-life balance. Our people are the key to our success. At RoslinCT we focus on developing our corporate culture, people's development, growth, and the ability to impact patients. ACCELERATING YOUR FUTURE The QC Analyst II, Flow Cytometry & Molecular Team, will be executing analytical method transfers to Quality Control, optimize and troubleshoot assays for improvement. He/she will be responsible for authoring Standard Operating Procedures (SOPs) and Test Methods. He/she will be executing various quality control methods, analyzing data, and reporting data. He/she will assist in the implementation of new assay methodologies and the associated instrumentation. Identifies and supports initiation and completion of deviations, corrective and preventative actions, and laboratory investigations in compliance with all applicable quality systems and current cGMPs. This position is highly visible in the organization and requires the ability to interface with multiple groups, and the ability to assess method suitability, interpret results, perform tasks independently, and troubleshoot. HOW YOU WILL MAKE AN IMPACT • Perform routine and non-routine quality control testing on in-process samples and finished products. • Operate and maintain laboratory equipment and instruments, ensuring proper calibration and adherence to cGMP Compliance. • Provide support for method transfers/qualification/validation and stability testing. • Support analytical equipment installation and qualification • Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner. • Review all data in accordance with applicable procedures and cGMP requirements. • Author, review, and/or approve SOPs, Test Methods, and other procedures required to operate a QC laboratory. • Participate in internal and external audits, inspections, investigations, change controls and CAPAs • Contribute to continuous improvement initiatives, identifying opportunities for efficiency gains and process optimization within the quality control function. • Anticipate and troubleshoot problems. Communicate effectively with management regarding task completion, roadblocks, and needs. • Become a qualified trainer on assigned assays and deliver training to analysts, documenting training per procedural and cGMP requirements. • Work independently in a high-paced team environment, meet deadlines, and prioritize work from multiple projects. • Communicate effectively with cross-functional peers, and department management. WHAT YOU WILL BRING • Bachelor's Degree in scientific discipline. • 3+ years of relevant experience in cGMP Quality Control Laboratory. • Hands-on experience with various analytical techniques such as flow cytometry, qPCR, dPCR, ELISAs, cell-based assays, and scientific knowledge in the characterization and transfer of analytical methods. • Hands-on experience with Raw Material sampling or system management is a plus. • Experience with rapid microbiological methods is a plus (e.g. mycoplasma) • Knowledge of cGMP/ICH/FDA regulations. • Ability to independently prioritize/manage activities. • Ability to prioritize objectives from multiple projects and adhere to scheduled timelines while maintaining flexibility and attention to detail. • Proficient in MS Office applications and information technologies that support documentation and data management systems. • Strong troubleshooting, problem-solving skills, oral and written skills. • Ability to multi-task and interact with multiple groups in a team-oriented environment. OUR COMMITMENT All RoslinCT employees embrace the principles of our culture and values and are deeply committed to fostering an environment where diversity and inclusion are not only valued but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. RoslinCT is proud to be an equal opportunity employer, we seek to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or any other applicable legally protected characteristics.

Job Details GARDNER, MADescription PRIMARY OBJECTIVE OF THE JOB Quality inspectors approve in-process product by confirming specifications, conducting visual and measurement tests, communication required adjustments to operator and/or production supervisor. Approves finished products by confirming specifications, conducting visual and measurement tests, returning products for re-work and confirming re-work. Documents inspection results by completing reports and logs Keeps measurement equipment operation and notifying QM should repairs be warranted. Qualifications SKILLS THAT ARE NEEDED · Technical Skills · Numerical Skills · Problem Solving Skills · Planning and Organizational Skills · Excellent knowledge of testing, inspection and measuring · Knowledge of Customer's Workmanship Specs · Knowledge of both UL and CSA Requirements · Must be able to read and write English · Multi-task · Must be able to work independently · Must be able to work well under pressure in a fast paced environment

The QC Inspector will report directly to the QC Inspector Lead, QC Manager or Director. This position is responsible to actively participate in the Repligen ISO 9001 Quality Management System. This role is responsible for inspecting, auditing, and reporting on incoming materials and processes using various visual techniques and measuring equipment to ensure conformance to the organization and customer quality standards. Responsibilities Conduct inspection of materials, from suppliers, and approves or rejects according to documented processes. Verify and apply part number label(s) to approved materials according to the inventory part labeling specification. Requires demonstrated use of inspection tools (i.e.: Calipers, Micro-hite, Comparator etc.) Able to assess and interpret engineering drawings, specifications, purchase orders, statement of work and standards to determine quality status. Knowledge of performing on machined parts based on drawing requirements using precision measuring tools. Aware and follow SDS (Safety Data Sheets) related to chemical handling of materials. Working knowledge of Geometric Dimensioning and Tolerancing GD&T. Working knowledge of sampling plan(s). Requires verbal or written communication to management of all Non-Conforming Material. Lead any non-conforming material and support Root Cause Investigations to closure. Good organization skills and Microsoft Office software to accurately document and maintain associated paperwork and inspection results in a consistent and timely fashion. Identify and communicate continuous improvement opportunities for the quality program for customers internal and external. Supporting First Article Inspection (FAI). Support Internal, Supplier and Customer Audits. Supporting Corrective Action, Deviations and Complaints. Maintain clean and orderly work area/ station. Comply with safety regulations and personnel policy. Other duties as assigned. Qualifications High School diploma or Two-year technical degree or equivalent from an accredited technical institution is preferred. Machine shop experience in the quality discipline or a related field will be considered. Familiar with medical devices, bioprocessing equipment, military or aerospace industry inspection practices and standards. Requires demonstrated use of basic Microsoft Office tools (Outlook, Excel, Word) Minimum 1-3 years' experience in Quality Assurance in an ISO 9001 certified Quality Management System or equivalent. Ability to communicate with multiple departments and associates. Shares timely information with peers on daily progress. Ability to contribute to project teams. Focus and attention to detail is critical. Understanding of Good Documentation Practices preferred.

The Quality Technician performs quality control tests/inspections on products at various stages of production process. Duties require verbal and written communication ability, visual acuity to product detail, manual coordination to operate hand tools and testing equipment, ability to enter data in computer system and the physical ability to lift various weights. Essential Job Functions Performs quality check of printed, laminated and slit roll samples and pouches on a regular basis to verify Operator's result for dimension. Operates quality control testing equipment/tools. Collects and manages sample retained. Collaborate with Operator and Production Supervisor in ensuring product conformance during job set up for approval to run. Respond and assist Production and/or Quality Supervisor in verifying reported non-conformities for quick resolution or corrective action. Communicate deviation incidents to concerned personnel for corrective action. Place non-conforming raw materials, WIP & Finished products ON HOLD/Quarantine on Radius, update the Quality Log and communicate to concerned personnel. Assist Quality Supervisor in sampling and verification of internally quarantined and customer returned non-conforming materials to identify proper disposition. Generates and issues Certificate of Analysis directly to customer or save in the system. Communicates discrepancies of production documentations (WI, SOP, Layout, etc.) to Management and CSR for timely correction. Prints quality forms for production personnel if needed. Read and replies to e-mails in timely manner. Cooperate in the maintenance, cleanliness and organization of the Laboratory. Cooperate during root cause analysis to identify proper corrective & preventive action. Assist in collection, preparation and review of customer required samples. Perform filing of quality documents/records. Assist with team members with their responsibilities as needed or during their absence. Attend team meetings and feedback on any quality related issues/improvements. Assist in employee trainings, if required. Follow all established safety rules and regulations and utilize required safety equipment. Report defective equipment or unsafe conditions to the appropriate personnel. Maintain work area in a clean and orderly condition. Follow all company Good Manufacturing Practices & Policies. Perform other duties as required or as requested by Supervisor or Manager. Ability to work a flexible schedule if needed. Ability to collaborate and maintain Garlock's commitment to a Food Safe environment. Skills and Knowledge Technical or vocational degree is a plus. Able to consistently act independently and prioritize work. Practical interpersonal and written communication skills Experience with ERP and other Maintenance Planning tools. Strong analytical and problem-solving skills Strong sense of ownership, work ethic, good judgment, and decision-making skills Familiar with Microsoft Office (Word, and Excel). Able to work in a fast-paced environment and multi-task effectively. Excellent organizational and prioritization skills. Excited about taking on new challenges in the manufacturing industry Self-motivated, hands-on, practical mindset, and capable of setting and reaching ambitious goals. Ability to work as part of a team and independently. Ability to collaborate and maintain Garlock's commitment to a Food Safe environment. Physical Requirements: While performing the duties of this job, the employee is regularly required to stand, walk, sit, and use hands to handle or feel. The employee frequently is required to talk or hear. The employee is occasionally required to reach with hands and arms. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Work Environment: The noise level in the work environment is usually loud. Period lifting of pallets weight and material weighing up to 50lbs Squatting, crouching, turning, twisting, stretching, climbing steps, grabbing, pulling, pushing, and bending. Visual and hearing acuity within normal limits Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Typical environment of manufacturing and production facilities. Exposure includes but is not limited to continuous noise, scent of materials, bright workstations, machinery with moving parts. Other Details: Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. This company is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.

Are you passionate about precision and quality? Join our team as a Quality Control Inspector, where you'll play a key role in ensuring our industry-leading mixing components meet the highest standards. In this role, you'll meticulously inspect parts using Coordinate Measuring Machines (CMM) and other precision tools, keeping detailed records and identifying areas for improvement. You'll collaborate with Engineering, Manufacturing, Production, and our vendors to enhance quality and drive cost savings. If you have a keen eye for detail and enjoy working in a team-driven environment, we want to hear from you! Quality Control Inspector Essential Functions: * Perform daily receiving inspections of manufactured components * Perform In process and First piece inspections of in house manufactured components * Follow established Admix and Quality Control Standard Operating Procedures to perform QC inspections * Record and maintain detailed and accurate inspection reports * Set up and perform inspections using manual CMM * Set up and run part programs on DCC CMM using PC-DMIS * Daily use of Sage100 ERP software * Utilize the Quality Control and Corrective Action databases * Final inspection of mixers before shipping * Setup and operation of the Laser marker * Some occasional travel will be required to inspect tank/mixer assemblies at other manufacturing facilities Quality Control Inspector Qualifications: * Knowledge to interpret mechanical drawings using current ASME Y14.5M Dimensioning and Tolerancing standard * Strong math skills to include algebra, geometry & trigonometry * Experience with creating part alignments on CMM using PC-DMIS CAD ++ 2018 * Basic knowledge of Statistical Process Control (SPC) * Knowledge of use and best practices of hand-held precision measuring equipment * Experience with Microsoft Windows, MS Office products * Must be self-motivated and capable of working with little supervision * Must be strong in multitasking and capable of prioritizing workload * Strong attention to detail * Excellent communication skills - both verbal and written * Must be able to work independently as well as part of a team * Must be able to lift 50 pounds Quality Control Inspector Education and Experience: * 3-5 years of Quality Control experience is preferred and/or * Associates degree Benefits and fun perks! * Medical, dental, and vision insurance * Company paid short-term and long-term disability, life, and AD&D insurance * 401k - 4% match * Employee Stock Ownership Plan (ESOP) * 11 paid holidays * 2 Floating holidays * Paid Time Off * 9/80 work schedule (April through October) * 10 volunteer hours * Employee Assistance Program (EAP) * Breakfast Fridays * Annual family day * Annual team building event * Annual holiday event * Too much to mention! Come grow with us!! Admix is an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. Admix participates in E-Verify.

Connexion’s mission is to provide "best in class" services to job seekers. We strive to achieve excellence in job placement, staffing, and recruiting services while treating candidates with the professionalism and respect they deserve. Title: Inspector, Quality Control Hiring Organization: Connexion Systems & Engineering Duration : PERM Pay rate : $18-22/hr Job Location : Bedford, MA Job# 16541 Overview Complete in-process, final inspection of medical devices and review DHR and record QC Chemistry and Microbiology results. Responsibilities Read work instructions to complete in-process and final inspections. Use a wide assortment of QC inspection instruments to assure components and devices are manufactured and are functioning in accordance to specifications. Use simple test equipment and record data and interpret its pass/fail status. Qualifications High school plus 1-3 years of related experience in inspection Experience with medical devices Clean room experience is a plus Familiarity with Quality Systems is preferred Please use the apply button to submit your resume for consideration. A Connexion Representative will contact you immediately. When responding to this job posting you MUST include the Job# and Job Title in your subject line. If you are active in a job search but this job is not for you, please reach out to . We would be glad to help you find the perfect job!

Acute Care Technology At ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions. The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Products include AEDs, trauma kits, ventilators, temperature management solutions, and more. Our dedicated employees take pride in their commitment to improving patient outcomes while delivering world-class customer service. At ZOLL, you won't just have a job. You'll have a career-and a purpose. Join our team. It's a great time to be a part of ZOLL! Job Summary Primarily responsible for Shipping QC which involves verification of packaged materials, sub-assemblies, finished products inspected to Quality procedure and Quality Standards. This may include verification of conformance to established standards and specifications. Reviewing picked items and verifying their accuracy to released orders. This position will also require cross training with Incoming Inspection as secondary tasks when there is no shipping product to inspect. This includes the verification of procured materials, sub-assemblies, finished products and processes to the companies Quality Standards. This may include visual inspection, dimensional measurement, and electrical testing to verify conformance to established standards and specifications. Must be willing to work 2nd shift hours: 3:00-11:00 PM EST. Essential Functions Shipping: * Perform visual inspection of shipping material & products according to established procedures. Parts for review will be verified against the sales order and Agile requirements. * Document inspection results using electronic storage system. * Maintain electronic quality documentation files such as, inspection records, within an electronic database. * Read and interpret documentation such as Standard Operating Procedures (SOP), PDAs and ECOs. * Items to be verified include but are not limited to the following: Serial Numbers of Devices, Parts and accessories included in the shipments, Date Codes, Batteries, and Lot Numbers. * Interface with other functions and departments as required. Incoming Inspection: * When required perform Incoming Inspection activities. * Inspect, measure and/or test manufactured devices to established methods and standards. * Utilize various inspection tools, such as rulers, DVMs, Power Supplies, Defib/Pacer Analyzers, custom fixtures etc. per procedures to backup QC inspection. * Inspect measure and/or test material to established methods and standards. * Utilize various inspection tools, such as Vision System, Verniers, Micrometers, Rulers, DMMs, Power Supplies, Defib/Pacer Analyzers, custom fixtures etc. per procedures. * Document inspection and test results according to established procedures. * Maintain quality documentation files such as, Device History Records (DHR) and Inspection History Records. * Process returned material to established procedures. Required/Preferred Education and Experience * High School Diploma or equivalent required * 0 to 3 years' experience in a related position required * Oracle and MES experience preferred Knowledge, Skills and Abilities * Good written and oral communication skills * Ability to read procedures * Good written and oral communication skills. * Ability to read specifications, procedures and engineering drawings. * Familiar with use of mechanical and electronic test equipment. * Basic computer skills: Microsoft Office, Oracle and MES. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. * Standing - Constantly * Walking - Constantly * Sitting - Occasionally * Lifting - Constantly * Carrying - Constantly * Pushing - Constantly * Pulling - Constantly * Talking - Occasionally * Hearing - Frequently * Repetitive Motions - Constantly * Eye/Hand/Foot Coordination - Constantly Working Conditions * Extreme cold - Occasionally * Extreme heat - Occasionally * Humidity - Occasionally * Wet - Occasionally * Noise - Frequently ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients's lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives. ZOLL Medical Corporation appreciates and values diversity. We are an Equal Opportunity Employer M/F/D/V. ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990 #LI-LV1 All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Acute Care Technology At ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions. The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Products include AEDs, trauma kits, ventilators, temperature management solutions, and more. Our dedicated employees take pride in their commitment to improving patient outcomes while delivering world-class customer service. At ZOLL, you won't just have a job. You'll have a career-and a purpose. Join our team. It's a great time to be a part of ZOLL! Job Summary Primarily responsible for Shipping QC which involves verification of packaged materials, sub-assemblies, finished products inspected to Quality procedure and Quality Standards. This may include verification of conformance to established standards and specifications. Reviewing picked items and verifying their accuracy to released orders. This position will also require cross training with Incoming Inspection as secondary tasks when there is no shipping product to inspect. This includes the verification of procured materials, sub-assemblies, finished products and processes to the companies Quality Standards. This may include visual inspection, dimensional measurement, and electrical testing to verify conformance to established standards and specifications. Must be willing to work 2nd shift hours: 3:00-11:00 PM EST. Essential Functions Shipping: Perform visual inspection of shipping material & products according to established procedures. Parts for review will be verified against the sales order and Agile requirements. Document inspection results using electronic storage system. Maintain electronic quality documentation files such as, inspection records, within an electronic database. Read and interpret documentation such as Standard Operating Procedures (SOP), PDAs and ECOs. Items to be verified include but are not limited to the following: Serial Numbers of Devices, Parts and accessories included in the shipments, Date Codes, Batteries, and Lot Numbers. Interface with other functions and departments as required. Incoming Inspection: When required perform Incoming Inspection activities. Inspect, measure and/or test manufactured devices to established methods and standards. Utilize various inspection tools, such as rulers, DVMs, Power Supplies, Defib/Pacer Analyzers, custom fixtures etc. per procedures to backup QC inspection. Inspect measure and/or test material to established methods and standards. Utilize various inspection tools, such as Vision System, Verniers, Micrometers, Rulers, DMMs, Power Supplies, Defib/Pacer Analyzers, custom fixtures etc. per procedures. Document inspection and test results according to established procedures. Maintain quality documentation files such as, Device History Records (DHR) and Inspection History Records. Process returned material to established procedures. Required/Preferred Education and Experience High School Diploma or equivalent required 0 to 3 years' experience in a related position required Oracle and MES experience preferred Knowledge, Skills and Abilities Good written and oral communication skills Ability to read procedures Good written and oral communication skills. Ability to read specifications, procedures and engineering drawings. Familiar with use of mechanical and electronic test equipment. Basic computer skills: Microsoft Office, Oracle and MES. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Standing - Constantly Walking - Constantly Sitting - Occasionally Lifting - Constantly Carrying - Constantly Pushing - Constantly Pulling - Constantly Talking - Occasionally Hearing - Frequently Repetitive Motions - Constantly Eye/Hand/Foot Coordination - Constantly Working Conditions Extreme cold - Occasionally Extreme heat - Occasionally Humidity - Occasionally Wet - Occasionally Noise - Frequently ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients's lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives. ZOLL Medical Corporation appreciates and values diversity. We are an Equal Opportunity Employer M/F/D/V. ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990 #LI-LV1 All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Acute Care TechnologySee attached Job Description for Quality Control I At ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions. The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Products include AEDs, trauma kits, ventilators, temperature management solutions, and more. Our dedicated employees take pride in their commitment to improving patient outcomes while delivering world-class customer service. At ZOLL, you won't just have a job. You'll have a career-and a purpose. Join our team. It's a great time to be a part of ZOLL! Job Summary Verification of procured materials, sub-assemblies, finished products and processes to the companies Quality Standards. This may include visual inspection, dimensional measurement, and electrical testing to verify conformance to established standards and specifications. Essential Functions Inspect measure and/or test material to established methods and standards. Utilize various inspection tools, such as Vision System, Verniers, Micrometers, Rulers, Oscilloscopes, DVMs, Power Supplies, Defib/Pacer Analyzers, custom fixtures etc. per procedures. Document inspection and test results according to established procedures. Maintain quality documentation files such as, Device History Records (DHR) and Inspection History Records. Process returned material to established procedures. Read and interpret documentation such as Standard Operating Procedures (SOP), schematics, technical drawings, PDAs and ECOs. Interface with other functions and departments as required. Required/Preferred Education and Experience High School Diploma Or equivalent. required 1-3 years experience in a related position. required Knowledge, Skills and Abilities Good written and oral communication skills. Ability to read specifications, procedures and engineering drawings. Familiar with use of mechanical and electronic test equipment. IPC-A-61OD for Incoming Inspection, preferred. Basic computer skills: Microsoft Office, Oracle and MES. Physical Demands Ability to lift up to 50 lbs. ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients's lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives. ZOLL Medical Corporation appreciates and values diversity. We are an Equal Opportunity Employer M/F/D/V. ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990 #LI-LV1 All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Reads and interprets work instructions and blueprints to determine dimensions and tolerances. Interprets Geometric Dimensioning & Tolerance. Measures, inspects, tests and verifies machined, welded and finished parts for conformance to specifications. Manually operates CMM's, height gages, comparator, etc. Provides support for quality projects dictated by the Quality Leadership. ESSENTIAL FUNCTIONS AND RESPONSIBILITIES Supports First Piece, In-Process, Final, and F.A.I. Inspections. Reads blueprints or specifications to determine dimensions and tolerances. Verifies specified dimensions of product or raw material using verniers, micrometers, intramics, CMM, height gages, comparator, scales and or/other tools. Measures angular dimensions, radii, height, thickness, location, thread lead, and other specifications. Computes angles, radii, and other unspecified dimensions of work piece by using sine bars. Measures surface finish of parts. Inspects first run parts and assemblies. Examines material or product for surface defects such as cracks, pits, and incomplete welds. Tests units for fit of moving parts and mechanical functioning. Tests parts for hardness. Compares product with parts list or sample model to ensure completion of assembly. Rejects defective parts, and marks type of defect on part, container of parts, or inspection tag. Writes reports regarding inspection and testing results. Manually operates and sets up Mitutoyo CMM's and FARO Arm. Supports inspection duties, quality objectives, and the Quality Management System. Studies blueprints, sketches, drawings, manuals, specifications, or sample part to determine dimensions and tolerances of finished work piece, sequence of operations, and setup requirements. Verifies conformance of finished work piece to specifications. Assists in other areas in support of product conformity. Facilitates effective communications and working relationships (including answering department phone). Demonstrates responsibility and accountability for creating a professional, safe, and clean environment evidenced by: being at work on time to perform assigned duties, following the policies of Granite State Manufacturing, always wearing safety glasses in designated areas, maintaining a neat and orderly work area, and following safety practices to prevent errors. Demonstrates commitment to teamwork by establishing effective relationships and networks with both managers/directors and workers, and collaborating with them to accomplish shared purposes and goals. Abides by GSM Code of Ethics and Business Conduct standards and strictly observes all U.S. and foreign laws and regulations. AAP/EEO STATEMENT Granite State Manufacturing (GSM) is an affirmative action and equal opportunity employer. GSM does not discriminate on the basis of race, color, religion, sex, gender, gender identity or expression, national origin, citizenship, veteran status, age, physical or mental disability, genetic information, marital status, sexual orientation, or any other consideration made unlawful by applicable federal, state, or local laws in its programs, activities, or employment. SEARCH / RECRUITING AGENCIES Granite State Manufacturing (GSM) does not accept non-solicited resumes or candidate submittals from search/recruiting agencies unless GSM requests such resumes, and the search/recruiting agency is on GSM's approved list of such agencies. Unsolicited resumes or candidate information submitted to GSM by search/recruiting agencies shall become the property of GSM and if the candidate is subsequently hired by GSM, GSM shall not owe any fee to the submitting agency. Requirements Two-year certification from college or technical school; or 5 years related experience and/or training; or equivalent combination of education and experience. Ability to manually operate and set up Mitutoyo CMM's. Must know how to interpret Geometric Dimensioning & Tolerance. Must have the ability to work as a team player in a group or team environment and must be able to work independently without supervision. Must be flexible enough to work in all areas of operation per the direction of the Leadership. A personal and professional background sufficient to secure a Government Security Clearance is required. Advanced knowledge of inspection, plating & coating processes and raw materials a plus. Benefits Granite State Manufacturing offers a comprehensive benefits package to all GSM employees. Health & Wellness Programs Health Insurances (Medical, Dental, & Vision) Flexible Spending Accounts (FSA) Basic & Optional Life Insurance Short & Long Term Disability Employee Assistance Program Voluntary Worksite Benefits 401k Retirement Plan Paid Leave Tuition Reimbursement Workers Compensation …and much more.

Responsible for visually and mechanically inspecting a wide variety of mechanical products and the setting up of standard measuring equipment to verify product, material and equipment conformance to customer/company specifications. DUTIES AND RESPONSIBILITIES: 1. Works with complex blueprints, assembly prints and specifications; visually and mechanically inspects parts, subassemblies and assemblies on most company proudcts to ensure conformance to production specifications and quality standards. 2. Performs the more standardized incoming, first piece, in-process, final floor, or bench inspection on a variety of parts and products. Generates QC documents as required. 3. Sets up and performs complex mechanical inspections. 4. Uses surface plate setups to maintain correct geometry during inspections. 5. Uses such equipment as scales, vernier, height sticks, mocrometers, Rockwell tester, plug gauges, coordinate measuring machine and optical comparators while carrying out inspection procedures. 6. Prepares reports and summary sheets, makes calculations and plots graphs indicating rates of acceptance and rejection. 7. Notifies Inspections and Production Supervisors of quality problems. 8. Maintains work area and qeuipment in a safe, clean and orderly condtions. 9. May be called upon to perform production testing. 10. Performs other related duties as directed. All Job Posting Locations (Location) Woburn Remote Type On-Site EEO Statement Boyd Corp is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.