Quality Control Inspector Jobs in Milford, NH

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. Selected candidate will be subject to a post offer background check and must be able to maintain a Secret-level DoD security clearance. Digital Prospectors is an Equal Employment Opportunity (EEO) employer. All qualified applicants will receive consideration and will not be discriminated against on the basis of race, color, relegation, sex, sexual orientation, gender identity, national origin, age, veteran status, disability status, or genetic information; US citizenship is required. Digital Prospectors affirms the right of all individuals to equal opportunity and prohibits any form of discrimination or harassment. 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. ******************* Job #17497

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.

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 Entry Leominster - Leominster, MA Full Time None ManufacturingQC Inspector QC Inspector FLSA: Non-Exempt REPORTS TO: QC Manager VALUES We listen to our Customers. We rely on our Employees. We honor Integrity. We embrace Continuous Learning. We lead with Design. We create Value. We work to make the World better. POSITION OVERVIEW This position is responsible for conducting inspections and testing to guarantee that products meet the quality requirements established by the company. Also, ensure compliance with quality processes by quality and production personnel. RESPONSIBILITES: Use a variety of conventional tools to perform the position and instruments to verify dimensions to drawing specifications. Conduct in process and end of process inspections in different deparments to verify if product meets the quality criteria. Identify defects in surface, dimensional, visual and nonconformities (material, documentation and workmanship) to quality standards. Inform the production and quality team if any operation, product or material does not meet quality standards. Help to identify the root cause of any quality issue so they can be addressed efficiently and effectively. Record the findings using the tools and documentation assigned by the company. Monitor and validate that rejected product have been repaired. Perform audits using the AQL sampling method. Conduct internal audits to verify if processes are being followed. Attend production meetings, communicate quality issues and quality indicators. Promote a continuous improvement culture. Attend and participate in internal and external training and educational courses required by the company. Maintain a clean, well-organized workspace in line with 5s standards. Always follow health and safety requirements and bring to light safety concerns as soon as they arise. Conduct internal audits to ensure compliance with established processes if needed. Qualifications REQUIREMENTS: High School Diploma Minimal computer skills required. Must be neat and detail oriented. Must be willing to work overtime hours. PREFERRED REQUIREMENTS Previous quality experience is a plus. Ability to read and interpret engineering drawings and quality control plans is a plus. Bi-lingual a plus. Knowledge of the use of handheld measuring instruments a plus. Knowledge of reading blueprints a plus. Knowledge of welding operations a plus. PHYSICAL REQUIREMENTS: PHYSICAL DEMANDS NEVER OCCASSIONALLY .25 - 2.5 Daily HRS FREQUENTLY 2.5 - 5.5 DAILY HRS CONTINUOUSLY 5.5 - 8 DAILY HRS PHYSICAL DEMANDS NEVER OCCASSIONALLY .25 - 2.5 Daily HRS FREQUENTLY 2.5 - 5.5 DAILY HRS CONTINUOUSLY 5.5 - 8 DAILY HRS SITTING x WALKING

Are you a motivated individual seeking a new and exciting opportunity? Do you want to work in a supportive environment with room to grow? Do you want great pay and benefits while also having a good work/life balance? Then we want YOU! About Us: Haydon, Kerk and Pittman are three world class AMETEK brands that supply advanced linear and rotary motion solutions to a diverse mix of global customers. We are recognized as a leading manufacturer of brushed and brushless DC motors, stepper motor based linear actuators, precision Acme lead screw and anti-backlash nut assemblies, linear rail and guide systems, gearmotors, drives and complete custom automation sub-systems. We are looking to add a motivated Quality Control Inspector to our team. This position is responsible for the evaluation of customer returns (RMA's), incoming inspection, first article and final inspection. What will you do? On any given day, your responsibilities would include: * Ensuring that all incoming material and accompanying documentation from suppliers conform to specifications and requirements. * Providing production floor support for in-process and final inspection as required. * Evaluating customer returns (RMA's), logging them and communicating findings. * Performing and maintaining files for First Article amd Final Inspection. * Working cross functionally with Manufacturing Engineering, Operations and Customer Service. * Maintaining inspection fixtures and gauges and ensuring proper calibration status of these items as required. * Creating and recording SPC files to capture inspection data. You are a great fit if you have the following: * Ability to program MicroVu vision system for part inspection. * High level communication skills; both verbal and written (email). * Ability to read and understand engineering drawings (including GD&T). * Ability to use all common inspection equipment including micrometers, calipers, height gauges, comparator, go/no-go gauges, etc. * Strong computer skills including the ability to use common Microsoft Office software. * Good organizational mind set. * Previous manufacturing experience (required). * High school or equivalent education level and previous quality/inspection experience (required) * Ability to shift priorities as required. Why should you join our team? AMETEK offers competitive pay and a great benefits package including: * Excellent medical/dental/vision coverage * Flexible Spending Accounts * Short-term and long-term disability * Paid Vacation * 401(k) Retirement Plan with Company Match * Tuition Reimbursement * Employee Assistance Program * Safety Shoe and Safety Glasses Reimbursement Come join our team! Apply now! Compensation Employee Type: Hourly Salary Minimum: $50,000 Salary Maximum: $70,000 Incentive: No Disclaimer: Where a specific pay range is noted, it is a good faith estimate at the time of this posting. The actual salary offered will be based on experience, skills, qualifications, market / business considerations, and geographic location. For more information on AMETEK's competitive benefits, please click here. AMETEK, Inc. is a leading global provider of industrial technology solutions serving a diverse set of attractive niche markets with annual sales over $7.0 billion. AMETEK is committed to making a safer, sustainable, and more productive world a reality. We use differentiated technology solutions to solve our customers' most complex challenges. We employ 21,000 colleagues, in 35 countries, that are grounded by our core values: Ethics and Integrity, Respect for the Individual, Inclusion, Teamwork, and Social Responsibility. AMETEK (NYSE:AME) is a component of the S&P 500. Visit ************** for more information. We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class. Individuals who need a reasonable accommodation because of a disability for any part of the employment process should call ****************. Nearest Major Market: Manchester Nearest Secondary Market: Nashua

Job Title: QA Inspector - Receiving Job Type: Full-time Busek Co. Inc. (************** researches, 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 ************** Job 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. Key Responsibilities: 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 Qualifications: 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. 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

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.

Quality Inspector Competitive Pay + Shift Differentials 3rd Shift positions available in Exeter, NH. SIG SAUER, Inc. is a leading provider and manufacturer of firearms, electro-optics, ammunition, airguns, suppressors, remote controlled weapons stations, and training. For over 250 years SIG SAUER, Inc. has evolved, and thrived, by blending American ingenuity, German engineering, and Swiss precision. Today, SIG SAUER is synonymous with industry-leading quality and innovation which has made it the brand of choice amongst the U.S. Military, the global defense community, law enforcement, competitive shooters, hunters, and responsible citizens. Additionally, SIG SAUER is the premier provider of elite firearms instruction and tactical training at the SIG SAUER Academy. Headquartered in Newington, New Hampshire, SIG SAUER has over 3,400 employees across sixteen U.S. locations in three states, and four additional global facilities. SIG SAUER is certified a Great Place to Work. For more information about the company and product line visit: **************** Hiring immediately for Quality Inspectors working in our Exeter, NH R&D and Prototype facility 3rd Shift Schedule - Sun-Thurs 9:30pm - 5:45am - base rate plus 30% Shift Differential As a Quality Inspector, you play a critical role in upholding our reputation for precision, reliability, and innovation. Your expertise ensures that every component meets the highest standards, supporting the safety and performance in the field and beyond. The Quality Inspector is responsible for the performance of routine mechanical inspections per the technical documentation provided using pre-trained/determined methods to determine product acceptability. FLSA: Non-Exempt Job Duties and Responsibilities * Collect and review inspection data to ensure component integrity and investigate/resolve discrepancies found during part inspection. * Locate appropriate programs, load components into inspection equipment, run basic inspection programs, and report results. * Identify features for inspection and correctly assign dimensional values and tolerances specified in print to a given feature. * Regular on-site attendance/punctuality is a necessary function of this position. * May be required to work in other functional areas and/or facilities depending on business needs. * May be required to work overtime or alternate shifts based on business needs. * Miscellaneous duties as assigned. Education/Experience & Skills: * High school diploma or general education degree (GED); or related experience and/or training; or equivalent combination of education and experience. * Basic proficiency in blueprint reading. * Familiarity with and basic understanding of GD&T symbology assigned per ASME Y14.5. * Fluent in setup of simple parts and understanding of proper use of basic mechanical inspection equipment. * Must be able to clearly, concisely, and accurately convey ideas and information to others, both verbally and in written form. * Expected to contribute in primary areas of inspection for which training has been provided. * Strong time management skills. * Communicate effectively to supervision verbally and in written format regarding problems and corrective action. * Participate in 5S workplace organizational activities and maintain work area in accordance with 5S standard. Why Choose SIG SAUER? Compensation and Financial Benefits: * Competitive Pay * Annual Employee Bonus * 401k from Day 1, employer match at 100% for first 4% contribution, 50% match on next 2% * Short Term/Long Term Disability Insurance * Life Insurance & AD&D Professional Growth and Development: * Career Advancement Opportunities * Comprehensive Training Programs * Tuition Reimbursement * License to access online Training platform Health and Wellness: * Medical, Dental, & Vision Insurance (starts following 30 days of employment) * Vacation Time * Sick Time * Paid Holidays * 3 Floating Holidays * 2 Service/Volunteer Days Employee Perks: * Generous Employee Firearm PURCHASE or GIFT Program * Employee Discounts * FREE UNLIMITED Classes at the SIG SAUER Academy in Epping, NH, 50% discount for spouse/partners * Friends & Family Discounts * Annual Prescription Safety Glass Reimbursement * Annual Safety Shoe Reimbursement * Onsite Gym - Corporate HQ * Certified Great Place to Work Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by law. #Quality #QualityJobs #Inspectors #mechanicaldimensional #GDT #blueprints #SIGSAUER #Exeter

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!

Monitors the daily in-process production by performing visual, dimensional and functional inspections. Essential Job Duties and Responsibilities: Perform visual, dimensional and functional inspections in accordance with In-Process inspection procedures and documents in Control plan as required Dimensionally inspect product utilizing various measuring devices, such as calipers, micrometers, vision systems Document inspection data on appropriate records. Utilize computer to record statistical data Able to use day to day gaging used in QA Lab Able to recognize defects on the molded/assembled parts Able to read and follow requirements on a control plan Regular attendance, punctuality and professionalism Essential Qualifications: Follow procedures for retaining samples Notify Supervisor/Lead of any non-conformances. Follow procedures for product rejections Maintain cleanliness of work areas and Quality Control equipment Generate Labels for daily production retains/tailgates at the start of each shift Responsible for supervising the rework of nonconforming product in the hold area and performing final inspection on reworked product if instructed Maintain quality areas clean, neat and organized Other duties as assigned Ability to read, write and communicate in English Minimum 1-3 years prior experience in Quality Control Recommended 1 year experience in Plastic Injection Molding Environment Experience with precision measuring equipment Blueprint Interpretation skills. Must have computer skills and familiarity with Word and Excel programs Knowledge of SPC and ISO 9001 & 13485 system requirements Ability to pay close attention to detail Ability to work well with others and independently. Ability to read, write and communicate in English ADA Requirements: Stand, walk, bend, squat, twist, reach or otherwise move frequently Occasional repetitive motion and grasping Occasional climbing to reach areas on machines or racks Lift, move or otherwise transfer up to 50 lbs. occasionally, >20 lbs. frequently Typically sits, grasps items or performs keyboarding for occasional operation of a computer Exposure to typical machine shop physical hazards which may require respiratory protection At SMC Ltd. we recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. We know that our differences often can bring about innovation, excellence and meaningful work-therefore, people from all backgrounds are encouraged to apply to our positions. Please let us know if you require reasonable accommodations during the interview process. SMC Ltd. is an equal opportunity employer. M/F/D/V; this organization uses E-Verify. Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments. All applicants must be authorized to work in the US #IND #LI-JB1 8:00PM - 8:00AM Rotating schedule w/ every other weekend off

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.

Your role: Responsible for quality control inspection of products to the established quality standards to meet customer demand and expectations. Additionally, optimizing operations to realize maximum efficiency and productivity. Understands and follows all written documents including standard operating procedures (SOP's), forms, Test Methods, and Test Specifications. Ensures proper line opening and line closing for one or more complete operations, maintain a clean and organized work area, communicate to the manufacturing team of any issues or opportunities that may affect product quality, and adhering to company Environmental Health and Safety (EHS) procedures. Assignments are moderately complex, where judgment is required in solving problems and making recommendations. May involve choosing from two or more pre-defined alternative courses of action. Works under general supervision, with some instruction given for routine work and detailed instructions for new types of work or special projects. Requires basic knowledge of how the team is organized and how own tasks relate to the others in the team/ unit. Impacts team performance through reliability and accuracy of own work. Follow Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). Communicate with previous and following shifts the status of processes. Check the Material Lists and Lot #'s Coordinate material disposition activities in support of production requirements / consumptions. Perform Line Clearance of Materials & Equipment. Perform changeover activities Clean all material areas at the end of the shift. Maintain effective and professional communication with Supervisors, Operators & Management. Assist in relieving operators in tasks that do not impact your QC inspections (carts, materials, moving product etc.) Any other duties as assigned. Physical Attributes: Lift 50 lbs. while using company supplied safety equipment. Who You Are: Basic Qualifications: HS Diploma or GED equivalent 2+ years of quality control or quality assurance experience in a manufacturing environment Preferred Qualifications: Associates Degree or higher. Previous manufacturing experience Read, follow and understand operating procedures. Basic math and counting to large numbers without error. Willingness to learn multiple production operations and adjust quickly to new tasks. Computer related skills to perform data entry and print reports. Strong written and verbal communication skills. Experience working in a complex and fast paced environment. Proven problem-solving skills. Experience sharing and advancing best practices. Ability to drive change and challenge the status quo in a respectful/professional manner. Highly self-motivated, have an intense customer focus and be able to satisfy both internal and external customer requirements.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: * Responsible for quality control inspection of products to the established quality standards to meet customer demand and expectations. * Additionally optimizing operations to realize maximum efficiency and productivity. * Ensures proper line opening and line closing for one or more complete operations. * Maintains a clean and organized work area. * Communicates to the manufacturing team of any issues or opportunities that may affect product quality. * Impacts team performance through reliability and accuracy of own work. * Communicates with previous and following shifts the status of processes. * Verify and review paperwork for accuracy. * Check the Material Lists and Lot #'s. * Coordinates material disposition activities in support of Production requirements / consumptions. * Performs Line Clearance of Materials & Equipment. * Performs changeover activities. * Cleans all material areas at the end of the shift. * Maintain an Effective & Professional communication with Supervisors, Operators & Management. * Assist in relieving operators in tasks that do not impact your QC inspections (carts, materials, moving product etc.) * C Shift: Monday - Thursday 10pm - 6:30am. Who You Are: Minimum Qualifications: * High School Diploma or GED. Preferred Qualifications: * Excellent communication skills, both written and verbal. * Experience within manufacturing. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of our diverse team! If you would like to know more about what diversity, equity, and inclusion means to us, please visit ********************************************************

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.