Quality control technician jobs in New Hampshire

“WHEN YOU WORK FOR US, WE WORK FOR YOU.”Travel Cath Lab Tech Weekly Gross Pay: $2971.00 - $3171.00 Assignment length: 12 Weeks Minimum years of relevant experience in healthcare: 1 years Job type: Traveler Shift: Day (5x8) Certifications: ARRT(R)/BCLS/BLS - American Heart Association/RCIS Position Highlights 12-week travel contract Competitive weekly pay package Work with an experienced clinical and recruiting team Quick start options available (inquire for details) Titan Medical is looking for travelers to fill a Travel Cath Lab Tech position for a 13 week assignment in Exeter, NH! Call Titan for additional details. ************** Benefits Day-one medical, dental & vision insurance Loyalty bonus after 2,080 hours Life and short-term disability 401(k) with employer match Referral bonus up to $1,500 24/7 recruiter support Licensure and CEU reimbursement Experienced clinical team available to support you throughout your assignment Titan Medical App available on the Apple Store & Google Play Why Travel with Titan Medical Titan Medical provides access to thousands of travel nursing and allied health jobs nationwide. Your dedicated recruiter will help you: Build a strong traveler profile by improving your résumé and showcasing your skills Increase your chances of landing the assignment you want Travel with a top healthcare staffing company in the industry Ready to apply or want more information? Call ************** to connect with Titan Medical today!

Adecco Staffing is partnering with a reputable manufacturing facility in Peterborough, NH to hire Quality Control Inspectors for all shifts! This is a temp-to-hire or direct-hire opportunity, depending on your level of Inspection experience. The position offers competitive pay rates and the opportunity to join a growing company. Pay Rate: $17-$26 per hour, depending on experience and shift Schedules Available: 1st Shift Monday through Friday 7:00am-3:30pm, OT available 2nd Shift Monday through Friday 3:15pm-11:45pm, OT available 3rd Shift Sunday through Thursday 11:30pm-7:00am (paid for 8), OT available Job Summary: Responsible for ensuring the quality of processes and product within an assigned functional area. Essential Duties and Responsibilities: The following represent general inspection functions which may or may not be required depending upon the functional area in which you are assigned. Inspectors may be reassigned to a different sub function at any time based on the business need, and training will be provided. Perform dimensional inspection using mechanical and visual inspection equipment, such as an optical comparator, contour reader, dial indicators, inspection hand tools, surface plates, height gauges, air gauges, specialized bearing measurement equipment, and gauge blocks. Measure bearing assemblies and/or component features such as roundness, concentricity, perpendicularity, flatness, sphericity, surface finish, surface noise and vibration levels using specialized equipment. Complete basic control charts, run charts, prepare charts, and histograms. Read and understand drawings, specifications, procedures, standards and instructions. Write inspection rejection reports in accordance with company procedures, and maintain detailed inspection records using appropriate forms. Make recommendations regarding quality and manufacturing improvements as needed. Perform visual inspection of bearing assemblies, and/or bearing components, using microscope and the unaided eye. Communicate with Manufacturing & Quality personnel and other disciplines as required in a timely and professional manner. Why Apply? Competitive pay rates with the potential for overtime. Temp-to-hire or direct-hire opportunity based on your level of experience. Work in a high-level manufacturing facility with advanced equipment and processes. Training and growth opportunities available. If you are interested in this exciting opportunity and feel you have the skills to succeed, please apply today with an updated resume or call 603-###-####! We look forward to hearing from you. Pay Details: $17.00 to $26.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for Employers San Francisco Fair Chance Ordinance Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Setting: Hospital? Are you ready to take your expertise as a cardiovascular technologist to new heights? Join Jackson HealthPros as a cath lab tech (Cardiovascular Invasive Specialist) and play a vital role on a team that values your expertise-while enjoying the excitement of a new location. Earn full time pay and benefits while you assist physicians and other Cath lab personnel in conducting vital diagnostic tests and procedures; and operate advanced medical equipment to capture crucial images and data of the heart and blood vessels. What You'll Need: ARRT certified Radiologic Technologist Registered Cardiovascular Invasive Specialist (RCIS) certification from Cardiovascular Credentialing International (CCI) preferred. Must have 2 years' experience in a Cath Lab hospital setting BLS & ACLS Certification (American Heart Association preferred) State specific licensing when required Apply now and you'll be contacted by a recruiter who'll fill you in with the details. Benefits Designed for Travelers We deeply value your commitment to impacting others, that's why we offer a comprehensive and competitive benefits package starting your first day. Weekly, On-Time Pay because that's how it should be Full Medical Benefits & 401k Matching Plan 24/7 Recruiter: Your main point of contact available by text, phone or email Competitive Referral Bonuses 100% Paid Housing Available Travel & License Reimbursement Impacting the Quality of Care for Patients Nationwide As a healthcare professional with Jackson HealthPros, you get the flexibility, stability and growth you need with the satisfaction of impacting communities nationwide. Choose from a variety of career options including direct hire, temp-to-hire, and travel contracts in cities coast to coast. Get full-time pay, benefits, and relocation assistance (at no cost to you) in travel contracts that give you the freedom to explore, with the stability of a full-time job. Find your perfect match with ProVenture, our AI enhanced career app designed just for you. EEO Statement Jackson Healthcare and its family of companies are an EEO/AA Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sexual orientation, gender, gender identity and expression, national origin, age, disability or protected veteran status. We celebrate diversity and are committed to creating an inclusive environment for all of our associates. Join our team as a traveling Physical Therapist where you'll help patients recover from injuries and manage chronic conditions while experiencing life in a new location. Apply now and we'll connect you with a recruiter who'll reach out with more details.

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

75 Plumb Pak Drive, Winchester, New Hampshire 03470 United States of America **Why Oatey?** Since 1916, Oatey has provided reliable, high-quality products for the residential and commercial plumbing industries, with a commitment to delivering quality, building trust and improving lives. Today, Oatey operates a comprehensive manufacturing and distribution network comprised of industry leading family of companies: Oatey, Cherne, Keeney, Quick Drain, Hercules, Dearborn, GF Thompson, William H. Harvey, Masters, Contact, Belanger, Lansas, and Durgo. At Oatey, we're doing big things - and by joining us, you'll have the chance to do big things too. You can build a strong career in an innovative, inclusive, high-performance environment, with the confidence that your company cares - about you, our customers and our world. **Ready to make an impact in a place where you matter?** - **Position Summary:** Ensures the quality of all processes, procedures, materials, processes rework and finished products. Also performs scheduled tasks as support for environmental and safety functions with additional responsibilities as assigned. This position is a second shift 3:00PM-11:30PM Monday-Friday work schedule and reports directly to Quality Manager. **Position Responsibilities:** Conduct daily quality inspections in all departments to audit the following: Procedure compliance/documentation with ISO9001 quality systems. In-process quality inspections, using established procedures. Incoming inspection, including first piece inspection, verification of Supplier's Certificates of Analysis, etc. Validation of product quality conformance to specifications. Complete ongoing Reliability Testing to ensure current products continue to meet product performance and/or formulation specs. Provide disposition and segregation of rejected materials and/or products. Summarize data and provide appropriate reports. Maintains rework inventory. Provides samples and sample data. Maintain calibration/verification records for all lab testing instrumentation and hand-held devices. Prepare test pipes (go-no go Gauges) for fit testing. Supply manufacturing with calibrated measuring and test equipment. Provide organizational quality support by assisting with problem resolution on the shop floor which includes gathering information on any quality-related issues, conducting root cause analysis and providing resolution for non-conformities. Participate in manufacturing CIP meetings as the QA representative and in ongoing quality training of manufacturing and QA staff. Maintain good housekeeping in lab, office and storage areas. Maintain and keep organized all QA files and documentation for easy reference and ISO9001 documentation compliance. Other duties as assigned. **Knowledge and Experience** Good communication and organizational skills. Computer literacy with Microsoft Office software applications. Excellent problem-solving and analytical skills. Basic understanding of quality concepts including variation, process control and root cause analysis. Cooperative attitude toward co-workers and supervisors. Knowledge of various equipment used in a laboratory (Fill machines, pallet jack, box knife, batch gun, mix tanks, drum mover, microscope, viscometer, Gas Chromatograph, and computer). **Education and Certification** High School Diploma required. Associate's Degree in a business, engineering or scientific course of study or equivalent experience in a manufacturing or laboratory environment preferred. At Oatey we are committed to help our Associates grow their career. Apply today and grow with Oatey!

Our client located north of Keene, NH is looking for a CMM Programmer/QC Technician to join their growing team! High school diploma or equivalent 2-3 years of experience Strong attention to detail Proficiency with JobBoss2 ERP, Mitutoyo MCOSMOS and/or MeasurLink software preferred Benefits you will receive as the CMM Programmer/QC Technician: $26-$32/hour, depending on experience Full-time, first-shift schedule with some flexibility Excellent benefits For the CMM Programmer/QC Technician position your duties will include: Perform first article and in-process quality inspections and approvals Read andd interpret technical drawings to ensure requirements and standards are met Utilize various measuring equipment to ensure adherence to specifications Maintain documentation and prepare customer documentation packages Other tasks as assigned Do you have CMM and QC experience? We want to hear from you! To apply for this position, please email your resume to *****************, call ************ or apply online at *************** We are here to help! For your convenience, Masiello Employment Services offers phone & video interviews/meetings. We can't wait to virtually meet you!

Building the people that build the world. With platforms in HVAC and Detection and Measurement, SPX Technologies builds innovative solutions that enable a safer, more efficient, sustainable world. Through our RiSE talent development framework, we Reach, Identify, Strengthen, and Engage our employees to support them in their continued development. We're a global company of problem solvers, collaborators, and innovators, and our businesses build solutions that impact the world. As part of Detection and Measurement, Aids to Navigation, including Flash, Sabik Marine and Sealite, are leading providers of lighting and navigational aids for the marine, obstruction, and airfield end markets. Offering the broadest portfolio of solutions, we help people transverse the world safely by air, land, and sea. Summary Contribute to the overall success of SPX Aids to Navigation by utilizing, developing and advocating product quality control plans and working closely with manufacturing to ensure quality standards are met and issues identified before shipment. Duties: Follow safe work practices and procedures, and ensure a “safety first” culture in every task undertaken. Work closely with manufacturing to perform Quality Inspection and functional testing of production assembly against the requirements. Undertake in-process and final inspection of the manufactured goods and approve for dispatch. Utilize, advocate, develop, product quality control plans. Adhere to quality performance requirements, flag and drive issues to root cause solutions. Ensure effective detection and control on non-conforming goods. Perform roving in-process audit to ensure process control of production processes Ensure status of conforming and non-conforming goods are clearly identified Resolve returned material from customers by identifying root cause and dispositioning Assist in the identification and resolution of incoming material and manufacturing quality issues, contain parts or products as needed, sort parts for quality requirements. Identify, escalate and implement continuous improvement ideas Perform any other duties as reasonably directed. Minimum Position Requirements: Technical qualifications in relevant fields. Previous industry experience in a similar technical QC role. Ability to read and understand electrical wiring diagrams and engineering drawings. Knowledge and understanding of electrical standards are desirable. Relevant experience with ISO 9001 Quality Management System. Knowledge of LEAN manufacturing practices such as 5S, Kaizen, etc. highly desirable. Excellent attention to detail. Strong problem-solving ability. Strong interpersonal and communication skills (written and verbal) Strong organization skills, including time management, multitasking and prioritizing. Motivated, self-starter, uses initiative and resilience to drive outcomes. How we live our culture Our culture is at the center of what we do and, more importantly, who we are. Our core values set a standard for how we manage ourselves, and our Leadership Model sets the standard for how we engage with each other. Whether you are an individual contributor or you lead a large team, each of us leads at SPX. What benefits do we offer? We know that the well-being of our employees is integral. Our benefits include: Competitive and performance-based compensation packages and bonus plans Educational assistance, leadership development programs, and recognition programs Our commitment to embrace diversity to build a culture of inclusion at SPX We value different backgrounds, experiences, and voices at SPX, and we are committed to challenging ourselves, openly communicating, and striving to improve every day. We believe in creating an inclusive work environment where everyone has a voice and is encouraged to realise their fullest potential.

Job DescriptionDEKA R&D has an immediate opening for a Quality Control Inspector to work in a dynamic Medical Device Research and Development company. This position is a highly visible role with significant and direct impact on the development and success of multiple engineering projects. Responsibilities as a Quality Control Inspector: Interpret Mechanical and Electrical print reading and apply inspection best practices Operate CMM equipment and utilize various measuring tools for inspection of medical device components Communicate effectively and promptly across multiple projects to provide feedback on inspection of parts Inspect various mechanical and electrical components and assemblies through incoming inspection Interpret ASME Y14.5 and GD&T standards throughout the inspection process for compliance and best practices Provide feedback on inspection activities to improve efficient whether individually or in a cross-functional setting To be successful as a Quality Control Inspector, you will need the following qualifications: 3+ years of experience in a regulated industry CMM programming, Metrology and/or CQI certified is a plus Basic GD&T knowledge required, Advanced GD&T knowledge preferred Proficient with mechanical measuring equipment such as micrometers, calipers, optical comparator Ability to operate CMMs following precise instructions Inspection of soldered components and Printed Circuit Board (PCB) assemblies; IPC-A-610 certification preferred Computer skills and knowledge; ability to learn new software (Experience with Jira is a plus) About DEKA: One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age. Behind DEKA's brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored. Powered by JazzHR VAABeEHa8x

Collaborate with Innovative 3Mers Around the World Choosing where to start and grow your career has a major impact on your professional and personal life, so it's equally important you know that the company that you choose to work at, and its leaders, will support and guide you. With a diversity of people, global locations, technologies and products, 3M is a place where you can collaborate with other curious, creative 3Mers. This position provides an opportunity to transition from other private, public, government or military experience to a 3M career. The Impact You'll Make in this Role As a Quality Technician, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative people around the world. Here, you will make an impact by: * Support product quality, product development, process scale-ups, and production processes by performing standardized, specialized, or complex tests, measurements, and tasks on experimental or standard production. * Activities will focus on the appraisal of raw materials, semi-finished, and finished goods. * Ensures that 3M quality standards and procedures are met and maintained. * Teach plant personnel quality methods and measurement techniques. * Complete daily audits of the manufacturing floor, quantify and report the results. Run precision test equipment and report results. * Other quality related tasks as required. Your Skills and Expertise To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications: * High school diploma/GED or higher (completed and verified prior to start) from an accredited institution * One (1) year combined quality and/or laboratory experience in a private, public, government or military environment * One (1) year experience utilizing Microsoft Office (including Excel) Additional qualifications that could help you succeed even further in this role include: * Associates/Two Year Technical degree or higher from an accredited institution in a private, public, government or military environment * Three (3) years combined quality and/or laboratory experience * Equipment validation experience * Good written and verbal communication skills that include excellent data collection and management * Flexible and responsive to changing priorities; able to multi-task; good organizational skills; attention to detail and compliant behaviors Work location: * On-site Tilton, NH 3rd Shift schedule Travel: May include up to 5% domestic/international Relocation Assistance: Is not authorized Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status). Supporting Your Well-being 3M offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, 3M regularly benchmarks with other companies that are comparable in size and scope. Chat with Max For assistance with searching through our current job openings or for more information about all things 3M, visit Max, our virtual recruiting assistant on 3M.com/careers. Applicable to US Applicants Only:The expected compensation range for this position is $59,409 - $72,611, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate's relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: *************************************************************** Good Faith Posting Date Range 11/25/2025 To 12/25/2025 Or until filled All US-based 3M full time employees will need to sign an employee agreement as a condition of employment with 3M. This agreement lays out key terms on using 3M Confidential Information and Trade Secrets. It also has provisions discussing conflicts of interest and how inventions are assigned. Employees that are Job Grade 7 or equivalent and above may also have obligations to not compete against 3M or solicit its employees or customers, both during their employment, and for a period after they leave 3M. Learn more about 3M's creative solutions to the world's problems at ********** or on Instagram, Facebook, and LinkedIn @3M. Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties. Safety is a core value at 3M. All employees are expected to contribute to a strong Environmental Health and Safety (EHS) culture by following safety policies, identifying hazards, and engaging in continuous improvement. Pay & Benefits Overview: https://**********/3M/en_US/careers-us/working-at-3m/benefits/ 3M does not discriminate in hiring or employment on the basis of race, color, sex, national origin, religion, age, disability, veteran status, or any other characteristic protected by applicable law. Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly. 3M Global Terms of Use and Privacy Statement Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at 3M are conditioned on your acceptance and compliance with these terms. Please access the linked document by clicking here, select the country where you are applying for employment, and review. Before submitting your application, you will be asked to confirm your agreement with the terms.

CMM Operator/Programmer, ITAR and DOD Position **non-exempt** Perform mechanical inspections using Zeiss and Brown & Sharpe Coordinate Measuring Machines as well as micrometers, calipers, pin gages, etc. Ability to understand GD&T, read prints and complete inspection reports required. Proficiency in First Article, First Piece and In Process inspections preferred. Soft Skills: Detail oriented, communication, team oriented Experience: CMM (Coordinate Measuring Machine) experience required. Software Proficiency: Excel, Calypso, PC DMIS Education: Minimum HS Diploma Travel: None Hours: 7am - 3:30pm PPE: Steel toed shoes, glasses as required Shortlisting Preference: All Qualified Timeline for Review and Interviews: ASAP Additional Information All your information will be kept confidential according to EEO guidelines.

Job Title: Quality Technician Pay: $22-$25 per hour, depending on experience Hours: Monday - Thursday, 6:00 AM - 2:30 PM, and a half day on Friday! 36 hours a week! As a Quality Technician, you'll help ensure that all customer and company quality standards are met-from raw materials to finished goods. You'll work closely with the Quality Manager and other team members to support inspections, documentation, and compliance activities that keep operations running smoothly. What You'll Do As a Quality Technician, you will be responsible for: Reviewing and approving testing reports from third-party laboratories Maintaining up-to-date knowledge of ASME regulations and applicable industry codes Receiving and inspecting returned products to determine quality and return category Evaluating inbound goods, preparing documentation, and managing return transactions Using metrology hand tools and small test fixtures to perform mechanical inspections Collaborating with the MRB team to determine the disposition of nonconforming materials Supporting company quality standards and 6S organization practices Working independently with minimal supervision Performing additional duties as assigned by the Quality Manager What You'll Bring The ideal candidate for this role will have: High school diploma or equivalent (technical education preferred) At least 5 years of experience in a similar quality technician or inspection role Strong math and mechanical aptitude Ability to read and interpret blueprints Familiarity with ASME Section II and IV (preferred) Proficiency with Microsoft Office and general computer use Experience with ERP systems such as M2K (inventory moves, RGA processing, etc.) Excellent communication, organization, and time management skills Ability to lift up to 35 pounds and work in a fast-paced environment Why Join Us in Rochester, NH? Stable schedule: Enjoy a four-and-a-half-day workweek with Fridays ending early Great pay: Competitive hourly rate based on experience Career opportunity: Temp-to-hire position with long-term potential Affordable health and prescription coverage with no waiting period Employer benefits available upon permanent hire Ask about our Referral Bonus Program to earn extra cash! Location & Schedule This position is on-site in Rochester, NH and follows a Monday-Thursday 6:00 AM-2:30 PM, Friday half-day schedule. 36/HRS a week! Ready to Take the Next Step? If you're ready to start a rewarding career as a Quality Technician in Rochester, NH, apply today or contact our recruiting team to learn more. Don't wait - we're hiring now!

1. Qualifications: a. High school diploma or GED required b. Minimum 3 years of relevant quality experience, within ISO13485/GMP manufacturing environment preferred, within extrusion is a plus c. Demonstrated efficiency and competency in core and advanced methods and gages for the inspection of tightly toleranced products d. Ability to read and interpret Engineering drawings e. Demonstrate initiative and self-motivation to create efficiencies and improve productivity within the inspection process f. Able to adapt and apply inspection knowledge to an array of product geometries and materials g. Work independently and prioritize assignments h. Will receive ongoing training to support competency and growth within the role i. Will receive opportunity and training to support growth within QC 2. Basic Position Skills: a. Organization Able to react and maintain order and focus across shifting priorities and tasks b. Time Management Able to balances multiple responsibilities and create efficiencies within the inspection process and achieve due dates c. Critical Thinking Able to apply and adapt training and experience effectively to assigned tasks; ability to interact with data and identify risk d. Communication Able to contribute across the team and coordinate with and support others to achieve departmental goals e. Mature work ethic professional and positive attitude; provide constructive feedback and ownership to drive improvement within areas of responsibility 3. Reports to: Quality Supervisor 4. Primary job responsibility: The QC Inspector Level 2 is a mid-level position within the QC department for individuals who have demonstrated proficiency in all Level 1 competencies and responsibilities. The Level 2 Inspector utilizes core and advanced inspection methods and gages efficiently to perform inspections of extruded product across a broad range of product geometries and material to determine conformance to defined specifications. This position may include responsibility for an assigned Quality workflow and/or area of focus within an area of demonstrated expertise, efficiency and experience. 5. Essential functions of position: Perform Final Inspection for product Lot Release a. Prepare, follow, perform and document final inspections as defined on inspection paperwork for lot release b. Adapt inspection method techniques to accommodate the inspection of an array of products, including prototypes, profiles, multi-lumen and thin wall extruded tubes c. Demonstrate acceptable measurement error within inspection methods and techniques d. Assess conformance to defined specifications and requirements and identify and document non-conformance reports (NCR) e. Perform boundary inspections and actions as required to contain non-conforming product f. Complete thorough and detailed end-of-shift reporting Perform Start up and In-process inspection of manufacturing extrusion lines a. Prepare, follow and perform start-up and in-process inspections for multiple extrusion lines within a shift for an array of parts with varying degrees of difficulty relating to raw material properties, geometries, tolerances and methods b. React, adjust and communicate appropriately to challenges encountered during the extrusion process c. Identify and document non-conformances to defined specifications and requirements during the extrusion process d. Communicate inspection results and work with extrusion technician or operator to address non-conformances and at-risk product e. Identify, document, and perform boundary inspection to contain at-risk product encountered during the extrusion process Assigned Quality Workflow or Area of Focus a. Support assigned workflow or area of focus with accountability and action b. Create documented procedures and provide training as warranted c. Maintain appropriate documentation and tracking of workflow outcomes and performance as warranted d. Identify under performance and risk within the workflow and action needed to sustain and/or improve workflow outcomes and performance as warranted e. Coordinate and work with others as needed in support of assigned workflow f. Provide and maintain active communication and updates of assigned workflow to Quality Manager and/or Supervisor. Inspection Methods, Gages and Equipment a. Utilize pin gages, ring gages, calipers, rulers, vision systems, and other applicable gages as specified and within scope of training b. Utilize advanced inspection methods including automated OGP routines and advanced vision system techniques such as modeling and construction c. Recognize and respond to basic visual and dimensional quality indicators and erroneous data d. Create efficiencies within the inspection process e. Identify and report equipment and gages outside of calibration dates and exhibiting damage, wear, or malfunctions Documentation and Compliance f. Adhere to Good Documentation Practices (GDP) requirements g. Maintain accurate and complete records in all required documentation h. Follow defined processes and procedures appropriately and effectively identify gaps and/or misalignment with requirements i. Maintain product and lot traceability throughout the workflow and in all inspection documentation Safety and Housekeeping a. Follow all requirements and equipment safety procedures b. Identify and report safety hazards c. Keep work area clean and organized Communication a. Professional and courteous interactions b. Effective use of email and daily reporting to facilitate follow-up and action c. Proactive and constructive communication and support across the team to drive improvement and collaboration 6. Is the work described above checked by another individual? ? YES ? NO 7. Work Environment: a. Dynamic and fast-paced manufacturing floor, prone to interruptions b. Exposure to noise, high temperatures, moving machinery, and high-voltage equipment c. Clean room and gowning requirements Is the work described above checked by another individual? YES Consistent motor skills and other requirements of the position: Persistent: Standing: 10% Sitting: 75% Walking: 15% Consistent lifting of up to 35 lbs. Rarely lifting of 1 lb. Frequently Maximum carrying distance of up to 30 ft. Occasionally Reaching must be able to reach machines and/or materials up to 6 ft. from Frequently Kneeling N/A Climbing stairs N/A Repetitive motion right/left hand/wrist Frequently Repetitive motion right/left foot/ankle N/A Continuous arm motions Yes Must be able to avoid potentially moving which could cause injury Yes Must be able to grasp and move object consistently and regularly Yes Vision: intricate nature of work requires of 20/20 with or without corrective lenses Yes Must be able to use gaging equipment and tools Yes Must demonstrate to work productively and efficiently with others Yes Microspec offers competitive wages and benefits, including: Sign-On Bonus Comprehensive Health Insurance Matching 401K plan annually after 1 year Entry-level 2 weeks paid vacation 64 Hours personal/sick time (unused time paid out at the end of the year) Annual discretionary bonus Salary range-$26.50-$28.00 per hour based on experience 20% Second Shift Differential

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. This position will have the primary responsibility for daily formulation activities to ensure schedule activities are completed, formulation materials and equipment are maintained, as well as the responsibility for performing corrective and preventative actions. As a secondary function, provide troubleshooting expertise for manufacturing of products both internally and externally of the company. Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The basic duties and responsibilities include the following, but other duties may be assigned. Has ownership for the daily formulation activities to ensure scheduled all scheduled tasks/events are completed Is responsible for critical steps in the formulation process including but not limited to, lab setup and process flows, in-process testing, API dissolution and final QS while ensuring safety, batch integrity and prevention or errors that could lead to product and or finical loss Initiate the production of batch documentation used for engineering and cGMP production. Prepare and update Master Production Batch records and SOPs accurately for communicating and initiate the documentation change process for needed documentation changes Complete executed Batch Records accurately and completely prior to submission to supervision for review Comply with all area SOPs and ensure logbooks are completed, and adhere to cGMP requirements Author process deviations when these occur within the department, participate in investigations, and contribute to identifying corrective and preventative actions Cross train to increase technical skills across the department Accountable for timely communication to management and clients of issues, challenges as well as opportunities for process improvements. As a member of the manufacturing team, you will perform other manufacturing tasks for example filling, capping etc., as needed. Work with enabling groups to improve/implement processes. Other duties as assigned. Strong interpersonal skills Strong working knowledge of MS Office suite is preferable Attention to detail and positive attitude are key attributes Able to follow rules and regulations perfectly Works directly with aseptic and non-aseptic personnel. Works closely with Quality Assurance, MTS, Validation etc. Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Required: High School education or AS degree or BS degree in Chemical Engineering/ Bio Chemistry or other industry related discipline is preferred Experience and knowledge of formulation/compounding tools and equipment Minimum 1-2 year's work experience in a GMP environment preferably in fill finish pharmaceutical operations Demonstrated ability to prioritize multiple projects and activities Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs. #LI-KC1 Join us and be part of building the bridge between life changing therapies and patients. Let's talk future Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

Supports Quality Assurance and Control activities to ensure products and procedures meet all applicable internal and external requirements. Supports the administration and maintenance of quality systems. Provides support for quality projects dictated by the Quality Leadership. ESSENTIAL FUNCTIONS AND RESPONSIBILITIES * Supports the administration and maintenance of in-process inspection reports, final inspection reports, and First Article inspection Reports compliant with AS9102 using Discus inspection report software. * Maintain calibrated test equipment, ensures equipment is calibrated, validated and maintained properly, maintains the calibration system, prepare test data, and identify areas for improvement. * Reads and interprets work instructions and to determine dimensions and tolerances. * Reads blueprints or specifications to determine dimensions and tolerances. * Collates test data and drafts quality reports. * May interpret test results and compare them to the specifications and control limits in place while providing recommendations on the appropriateness of data. * Supports QMS activities including but not limited to CAPA, Internal Audits, Document Control, Records Management, etc. * Maintain QMS documentation; revise and update documentation, assign training based on documentation changes. * May interpret Geometric Dimensioning & Tolerance * Strong attention to detail, organization, and documentation skills. * May verify specified dimensions of product or raw material using verniers, micrometers, CMM, height gages, comparator, scales or other tools. * Assists in other areas in support of product conformity. * 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. * Complies with federal and state laws, regulations, specifications and company standards. * Abides by GSM Code of Ethics and Business Conduct standards and strictly observes all U.S. and foreign laws and regulations.

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 The Intermediate Level Membrane Analytical Lab Quality Control Technician supports the full operation of testing biopharmaceutical membranes with a focus on maximizing safety, quality, and productivity. This role involves assisting with intermediate level testing operations, including performing basic troubleshooting on set-ups and membrane testing processes, and requires a basic level of knowledge of the Laboratory Information Management System (LIMS). Duties include: * Test membranes safely and in accordance with Standard Operating Procedures, Quality and Safety Specifications and GMP standards. * Safely set up and operate quality lab test equipment and monitor required inputs and outputs. * Support quality lab operations and projects under the supervision of senior technicians. * Accurately complete documentation per GMP standards. * Initiate and participate in Out of Specification (OOS) investigations. * Assist with execution of protocols, qualifications, and validations. * Develop skills to independently perform membrane analytical testing. * Works under close supervision to perform basic troubleshooting and set-ups; review and verify test and process data for accurate entry into the Laboratory Information Management System (LIMS); participate in sustainability efforts; and proactively identify and actively report safety, quality, and productivity concerns, including hazardous conditions or behaviors observed in the working environment and on site. * Ensure a clean and orderly workspace. Physical Attributes: * Exposure to machinery and equipment, chemical reagents, biological materials at Biosafety Levels 1 and 2, in a laboratory environment. * 100% Standing and/or sitting for duration of shift, up to 12 hours. * Frequent lifting of 20 - 30 lbs. necessary/Max lifting - 40 to 50 lbs. * Ability to bend and twist as needed. * Must be able to grasp, manipulate and handle objects consistently and regularly, Fine motor skills are required. This is a B Shift position Monday- Friday 2PM-10PM Who You Are Minimum Qualifications: * 1+ years of laboratory or cGMP manufacturing experience. * High school diploma or GED. Preferred Qualifications: * Associate's degree in any discipline. * 2+ years of laboratory or cGMP manufacturing experience. * Aseptic laboratory experience. * Basic knowledge of EHS, ISO, cGMP, and other manufacturing regulatory requirements. * Basic computer skills, familiarity with Microsoft Office applications. * Reliable and self-motivated. * Read, follow and understand test methods, operating procedures and related documentation. Pay Range for this position: $22.00-$39.00 per hour The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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 a team that is dedicated to Sparking Discovery and Elevating Humanity!

Job Description The Quality Technician - FAI Specialist is responsible for coordinating and supporting the creation of AS9102 First Article Inspection Reports (FAIR) in alignment with industry and customer specific requirements. This position works alongside various other departments and is vital to ensuring success of the AS9102 program. Duties/Responsibilities: Navigates internal company software and database systems to gather information. Accurately completes AS9102 Reports (FAIR) and other dimensional inspection reports as required. Interpret drawings, specifications and customer requirements. Works effectively and communicates with various departments, including: Planning, Marketing, Quality, QC Inspection and Source Inspection. Assures accuracy of FAI programs and records. Assists with identifying opportunities for improvement within the FAIR process to aid in the success of the Quality Department. Maintain a positive work environment by acting and communicating in a manner so that you get along with customers, clients, vendors, co-workers and management. This position may require overtime for coverage on alternate shifts and weekends. Will be required to perform other duties as requested, directed or assigned. Requirements: High School diploma or General Education Degree (GED). Previous experience as a First Article Inspection Specialist is preferred but not required. Must be able to use a computer to maintain records, develop reports, and analyze data and document discrepancies as well as using a computer to perform all other related aspects of the position. Must have excellent communication skills and ability/flexibility to work in a fast-paced environment. Must be able to read and interpret technical drawings, prints and industry/customer specifications. Must be able to read and interpret GD&T requirements. Must be able to display a thorough attention to detail and organization. Amphenol offers a competitive salary and benefits. The candidate must be able to legally work in the United States; we are unable to provide sponsorship. Position requires candidate to be a U.S. person as defined in ITAR, 22 CFR 120.15 (U.S. Citizenship or Resident Alien Status) and defined by 8 U.S.C. 1101(a) (20). Amphenol is a proud Equal Opportunity Employer as to all protected groups, including Individuals with Disabilities and Protected Veterans. For consideration for this position, please apply online to: ********************************** APC878

Job Description Job Title: Quality Assurance Technician FLSA Status: Non Exempt Developing and maintaining company inspection reports. Inspecting goods or products according to quality and safety standards. Ensuring goods and products comply with company standards as well as Federal and State law. Ensuring test equipment is calibrated and working correctly. This is a 3rd shift position 11:00pm-7:00ajm Key Responsibilities Responsible for maintaining high customer product acceptance through ensuring that products shipped adhere to product specifications at all phases of the operation. This includes inspecting incoming raw materials, purchased parts and outside service (OV) parts. In-process and final product acceptance, first article inspections and dock audits are also required. Responsible for maintaining process acceptance through auditing production process at all phases of production. This auditing will include, but not limited to: 1st pc process, Frequency process, Setup process, Routing Audits, 5S Audits and Safety Audits, all as applicable. Responsible as required, for training machine operators in inspection of product as determined by prints or support documentation. Must have a complete understanding of inspection tools and how to use them. (As applicable to building). Inspection and processing of Returned Goods (RAs), including required data entry, internal and external communications and required reporting. This includes sorting product as applicable. Responsible as required, participate in Root Cause Analysis (RCA) and Corrective & Preventive Actions (CAPA). Must be knowledgeable in the effective use of Lean Six Sigma (LSS) tools and concepts to assist in process improvements as required. Serve as an active participant in LSS programs that promote continuous improvement. Must be knowledgeable in ISO Standards and objectives to maintain and reinforce as needed. Responsible for maintaining and recording accurate quality documentation in various company data collection systems, including first piece sheets, certified operator documentation and in-process records. Must be able to work extended hours when required. Maintains a safe and clean working environment by complying with procedures, rules, and regulations. Contributes to team effort by accomplishing related results as needed. Performs all other duties as assigned. Required Qualifications Must be honest, reliable and conscientious. Task requires comprehension of high school math, reading, and writing skills. Must be able to perform computer work. Must be knowledgeable in Microsoft Excel, Word, e-mail and E2 database. Must be knowledgeable in Standard Operating Procedures as it relates to the Quality Department. Must be able to work well with others. Must be able to read and understand Fabrication blue prints and Machining blue prints including Basic GD&T.(As applicable). Tasks require walking, bending, climbing, lifting and standing. Tasks require the use of small hand tools, instruments and materials 60% of the time. Tasks require visual inspection and reading measurement tools and instruments. Tasks require flexibility and adaptability at a rapid pace Physical and Environmental Conditions Exposure to load noises Regularly required to sit, stand, bend, reach, climb and move about the facility Regularly operates a computer, computer accessories and phone equipment Required to occasionally lift up to 50 lbs. Occasionally stoops, kneels, reaches and carries this is a 3rd shift 11pm-7am Sunday through Thursday

Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. Security Clearance: None/Not Required Staff Quality Compliance Technician (Onsite) Joining Collins Aerospace isn't just about finding a job; it's about embarking on a journey to redefine the future of aerospace technology. Collins Aerospace, an RTX company, is a leader in technologically advanced and intelligent solutions for the global aerospace and defense industry. Collins Aerospace has the capabilities, comprehensive portfolio, and expertise to solve customers' toughest challenges and to meet the demands of a rapidly evolving global market. What You Will Do: Monitor and/or oversee the Quality Management System (QMS), processes, procedures, requirements, contracts and metrics, to ensure the organization's compliance. Prepare and maintain Quality systems (documentation, processes and training). Evaluate the compliance and effectiveness of the QMS of business sites, and programs. Work with other functions to ensure systems are compliant, efficient and can deliver to customer requirements. Develop, conduct, and support audits including providing feedback on non-compliance and corrective action(s). Determine if all products and processes are aligned with regulatory standards. Perform site audits Participate/shadow external audits (Nadcap, AS9100, 1st, 2nd party, and customers) Perform special process validation activity QMS Gap Analysis between customer and central quality requirements against site procedures. Manage site training database and training matrix Manage 5S program Create Quality Alerts Receive certifications from outside services Processing site procedures ECNs (Engineering Change Notices) May be required to perform other related duties, as necessary Qualifications You Must Have: AA/AS degree (or other 2-year post high school training) with a minimum of 6 years of relevant experience. Experience in a Quality/Compliance environment Qualifications We Prefer: Strong interpersonal and teamwork skills require minimal supervision. Strong organizational skills and ability to manage multiple projects concurrently. Good communication skills (written/verbal) with an aptitude for conveying complex technical information to a wide variety of audiences. Demonstrated ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to work effectively in a team environment to accomplish common goals and provide status as needed. Do you want to be a part of something bigger? A team whose impact stretches across the world, and even beyond? At Collins Aerospace, our Mission Systems team helps civilian, military and government customers complete their most complex missions - whatever and wherever they may be. Our customers depend on us for intelligent and secure communications, missionized systems for specialized aircraft and spacecraft and collaborative space solutions. By joining our team, you'll have your own critical part to play in ensuring our customer succeeds today while anticipating their needs for tomorrow. Are you up for the challenge? Join our mission today. What We Offer: Some of our competitive benefits package includes: Medical, dental, and vision insurance Three weeks of vacation for newly hired employees Generous 401(k) plan that includes employer matching funds and separate employer retirement contribution, including a Lifetime Income Strategy option Tuition reimbursement program Student Loan Repayment Program Life insurance and disability coverage Optional coverages you can buy: pet insurance, home and auto insurance, additional life and accident insurance, critical illness insurance, group legal, ID theft protection Birth, adoption, parental leave benefits Ovia Health, fertility, and family planning Adoption Assistance Autism Benefit Employee Assistance Plan, including up to 10 free counseling sessions Healthy You Incentives, wellness rewards program Doctor on Demand, virtual doctor visits Bright Horizons, child and elder care services Teladoc Medical Experts, second opinion program And more! Learn More & Apply Now! *Please ensure the role type (defined below) is appropriate for your needs before applying to this role. Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products. Regardless of your role type, collaboration and innovation are critical to our business and all employees will have access to digital tools so they can work with colleagues around the world - and access to Collins sites when their work requires in-person meetings. Apply now and be part of the team that's redefining aerospace, every day. As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote. The salary range for this role is 50,000 USD - 100,000 USD. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and key skills.Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement.Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance.This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply.RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window. RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act. Privacy Policy and Terms: Click on this link to read the Policy and Terms

Cath Lab Tech Location: New London, NH Agency: Nationwide Therapy Group Pay: $2,439 per week Shift Information: Days - 3 days x 12 hours Contract Duration: 13 Weeks Start Date: ASAP AlliedTravelCareers is working with Nationwide Therapy Group to find a qualified Cath Lab Tech in New London, New Hampshire, 03257! NTG is committed to matching you to the right position and we pride ourselves on our commitment to our travelers. This includes offering exceptional pay packages along with these great benefits: Medical, dental, and vision insurance Required Licensure, certifications, and CEU reimbursements Competitive 401K plan Great referral program Contact NTG for more information on this opportunity, compensation options, additional locations, and more! About Nationwide Therapy Group Nationwide Therapy Group is a recognized provider of healthcare staff across the country. We were founded by a former traveler who recognized the need for a transparent agency with a "traveler first" mentality. Not only are we recognized by Joint Commission, we are a certified minority/woman owned business. NTG has thousands of contract and permanent opportunities in all 50 states for nurses, therapists, and allied health professionals. Whether you're an employer in search of staff, or a job seeker looking for your next adventure, we have experienced staff here to help. 10855717EXPPLAT