Quality control analyst jobs in Wallingford Center, CT

There's never been a better time to join the shipbuilding industry. As demand for cutting-edge naval technology grows, General Dynamics Electric Boat is at the forefront-designing, building, and maintaining the most advanced submarines in the world. Our work is mission-critical, supporting the U.S. Navy and strengthening national security. Role Overview The selected candidate will support 3 rd shift Radiography Supervisors and General Foreman to ensure radiography operations are effectively planned, properly communicated, and executed with minimal disruption to shipyard schedules. The role focuses on developing complete and accurate work packages for various inspectional evolutions, performing site reviews to confirm readiness, gathering radiography performance data, and supporting continuous improvement initiatives. The candidate will also be expected to qualify for RT oversight duties, coordinate training activities, and manage required documentation submissions. Strong ability to read and interpret blueprints, specifications and procedures is essential. Key Responsibilities Develop comprehensive work packages for surveys, OPCON inspections, NDT inspections, and other radiography-related evolutions. Conduct deck-plate work site reviews to verify readiness, including staging, lighting, electrical needs, tank watch requirements, and other essential conditions. Coordinate planning and briefings to ensure affected personnel are properly informed prior to radiography operations Collect, analyze, and report radiography performance data - including re-inspection and rework metrics, to identify process roadblocks and improve execution Qualify to perform RT oversight and support ongoing radiography program requirements Schedule and track training for personnel involved in radiography operations Prepare and submit RT lots and related documentation to SupShip Interpret blueprints, specifications, and procedures to ensure technically accuracy and compliance Qualifications Required High School Diploma or GED 4+ years of experience working in technical, industrial, or inspection-related environments involving documentation and coordination 3+ years shipyard experience IRRSP qualified Preferred Previous experience with Quality inspection procedures and applicable SSPs is preferred. Experience working with EB's inspection activities and certification procedures Previous experience with a variety of RT and inspection documentation (SWSS/ERS weld tickets, CPJ 905 cards, RUT's, TIR's, ripouts, etc) is highly desirable Experience with EB's electronic systems (MQS, ERS, CPJ, Cornerstone, MS Office Suite) 5+ years shipyard experience including new construction and overhaul/PSA work Skills Excellent oral and written communication skills Must be able to resolve documentation problems Must possess independent thinking and problem-solving abilities Why Join Us We offer a workplace where integrity, innovation, and excellence drive everything we do Competitive Pay & Benefits - Comprehensive healthcare, retirement plans, and tuition assistance Career Growth - Training, mentorship, and opportunities to advance within the company Stability & Expansion - We're growing, adding thousands of new jobs across our facilities Inclusive Culture - Employee Resource Groups and community engagement Impactful Work - Every role contributes directly to national defense and the U.S. Navy's mission Physical Qualifications Climbing, Crawling, Kneeling, Medium Lifting, Pulling, Pushing, Reaching, Twisting We can recommend jobs specifically for you! Click here to get started.

IS IN MIDDLETOWN,CT Who is Habasit? Habasit is the global leader in the manufacturing of lightweight conveyor belting. Our slogan “Solutions in Motion” defines us; we are a provider of world class power-transmission and conveying solutions. At Habasit, we understand that a global leader is only as good as the people who represent it, and we are always searching for the right people to keep us in motion. We are looking for ambitious individuals, leaders, and students who are ready to help move us forward. If you have a can-do attitude and want to join a world-class organization, read on and apply today! We offer an attractive place to work and personal development in an empowering work culture. You will benefit from the expertise and opportunities of a solid global group of companies and the reputation of its products. Things you should know about Habasit's opportunities: Competitive Salary Excellent health insurance benefits which includes a bundled medical + dental package 401(k) program with up to 6% company match (at 100%) Tuition reimbursement (with Manager approval) Gym membership reimbursement Employee Assistance program Referral bonus OVERVIEW OF POSITION: Support R&D production trials and testing R ESPONSIBILITIES OF THIS POSITION - DEPARTMENT: Support of R&D production trials, which includes preparation trial documentation, attendance, and sample collection, labeling, and storage. Preparation of test samples from R&D production trials, which includes slitting and joining for tensile testing and wear and tear fatigue testing. Lab testing, which includes melt flow, tensile strength, wear and tear, coefficient of friction, abrasion, dimensional measurements … etc. Maintenance and upkeep of lab equipment, accessories, and supplies. Analysis and reporting of data and results collected from lab testing. Maintaining R&D inventory of production prototypes and shipping out of customer prepared samples for evaluation and field testing. COMPETENCIES/SPECIFIC EXPERIENCE OR TRAINING PREFERRED: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements/preferences listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Required - College degree. Required - Read, Write and Comprehend English. Preferred - R&D laboratory experience including polymer products testing, mixing of rubber or plastic materials. Preferred - Mechanical or chemical technician background. Preferred - Thorough understanding of MRP. Preferred - Microsoft Office, including Word, Excel, PowerPoint.

First shift 445am-3pm Monday - Friday with some Saturdays through the year Summary: The Quality Control Technician is primarily responsible for quality assurance of all products through administration of HACCP, GMP's, Sanitation, Pest Management and other programs that ensure regulatory compliance and education of staff. The position supports the Quality, Food Safety and SQF initiatives outlined in the Quality Manual and SQF Program. Essential Job Functions : Ensures specifications are met by measuring, recording, analyzing data and working with equipment and production personnel to improve results. Perform and document daily pre-op inspections and related checks. Assist Production Supervisor with daily line set up. Calibrate scales, thermometers, and water meters daily. Prepare all the necessary paperwork needed to complete documentation of all products and processes. Test, analyze, record, and control all product and component weights as well as sensory evaluations according to specified time intervals. Record and document all HACCP related processes. Report problems or deficiencies in quality or related processes to QA Manager and Shift Supervisor. Maintain USDA, HACCP, GMP guidelines on the production floor. Interact with USDA Inspectors. Work with Production Supervisors and personnel to maintain quality /customer standards. Pre-operations testing to ensure production is authorized to start. Ensure sufficient supply of items such as gloves, hairnets/beard nets, hearing protection, aprons, hand and shoe sanitizing stations, soap, and paper towel stations. Monitor all freezer and cooler temperatures. Monitor the temperature of the meet during cooking and cooling. Monitor the pasta hydration. Ensure all metal detection/X-ray devices are operating properly. Interact with outside technicians for scale and metal detection calibrations. Take product samples at scheduled times. May participate as member of Safety Committee. Participate in Allergen and Pest Management Program. Provide support for other positions when needed. Check and record sanitizer concentrations. Verify ingredients, lots, and quantities in production batches. Other duties as assigned. Job Requirements: High School diploma or equivalent. English, Bilingual preferred. 1-2 years of Production Line Experience within the food industry a plus. Product knowledge: Acquire and maintain full knowledge of USDA and FDA codes, rules, and regulations. Proficiency in follow-up; ability to meet deadlines. Team player, positive can-do attitude. Ability to assess situations and make independent decisions to achieve success. Ability to bend, sit and stand. Ability to perform multiple complex tasks concurrently. Ability to communicate both verbally and in writing. Ability to see and walk for inspections of plant sites. Ability to hear. Ability to lift at least 25 lbs.

JOB TITLE: Quality Control Inspector JOB CODE: Quality Control REPORTS TO: Quality Assurance Manager. Direct on-site project direction and daily scheduling provided through continuous communication with the applicable IMIA Project Manager and/or Supervisor. PAY RANGE: $32.00/hour- $42.00/hour based on experience Summary of position: Responsible for monitoring quality control/assurance requirements of all preservation preformed onboard commercial and US Navy vessel in accordance with established Navy regulations and industry standards or specific contractual requirements as defined in the Scope of Work. Collaborate with customer QA personnel on necessary aspects of the job. Essential Job Requirements: Produce/create electronic/handwritten Quality Assurance documentation as Objective Quality Evidence for work performed throughout the preservation process. Develop and Maintain Test and Inspection Plan (TIP) for all assigned jobs. Monitor and document all required readings with regard to, but not limited to, metal anchor tooth (profile), paint wet/dry film thickness (DFT), steel temperatures and all required environmental readings using appropriate equipment to include: micrometer, dry film thickness gauge, infrared thermometer, psychomotor. Ensure all assigned equipment is maintained in good working order with within all calibration certification intervals. All of the above requirements shall be completed in a safe and efficient manner so as not to cause injury to self or others. Required Education: High School diploma or equivalent Required Certification: NACE Inspector and/or SSPC NBPI required. Required Experience: Formal or informal on-the-job training in the marine industry; familiarity with Navy and Society for Protective Coatings standards. Required Skills: Must possess knowledge of Maritime paintings standards with particular emphasis in US Navy ship preservation criterion. Word processing, spreadsheet, email, and database computer skills required. Must be able to accomplish mathematical calculations associated with preservation readings and documentation; must be able to discern and carry out complex written, oral, or diagramed instructions. Must be able to take direction; interact professionally, knowledgeably and cooperatively with supervisors and co-workers and customer representatives. Physical Requirements: Must be physically capable of working an 8-10 hour day requires average use of computer, some physical dexterity, and agility within confined and restricted spaces & tanks. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform essential job functions. Supervisory Responsibilities: None Working Conditions: Regularly stand for long periods of time; work on scaffolds and ladders; work on top of machinery; work in confined spaces. Regularly exposed to extreme temperatures, high noise levels, toxic or caustic chemicals, fumes, airborne particles, outdoor weather conditions, dusty conditions, wet and/or humid conditions, hazardous machinery, precarious places, close proximity to other employees. Overtime or shift work involved. Travel often required. Must follow strict safety procedures.

The Senior Quality Control Technician role in our Bloomfield, CT facility drives improvement in the reliability of CO2 Laser products. The incumbent will be engaging directly with a cross functional team on a wide variety of products to ensure our product and processes meet the dynamic laser manufacturing requirements. Working with a quality mindset team, this role will provide hands on support for the incoming goods, in-process, and final inspection of laser systems to ensure we meet Coherent Quality Standards. Primary Duties & Responsibilities Inspection manufactured laser systems: Detail oriented inspection of electronic and mechanical assemblies Utilize common inspection methods to evaluate critical design requirements Develop inspection test plans with a cross functional team Assist in problem solving activities to support identified nonconformities Evaluation and verification of purchased components Define and execute incoming material test plans for qualification activities Document and present inspection results to key stakeholders Verification of vendor supplied documentation including first article inspections and material certifications Support of Quality Systems: Document detailed findings to be used for Continuous Improvement Initiatives Accomplish root cause analysis and provide corrective actions with follow-up Ensure practices align with best practices, procedures and inspection techniques Perform internal product and business system audits Reliability system maintenance: Utilize computers for automated data collection and control of instruments Collaborate with the Quality organization regarding calibration of test instruments Monitor and troubleshoot long term unmanned tests with engineering support Assist in developing new methods and protocols for component level testing and measurement Complete calibration of monitoring and measuring equipment support Education & Experience High School diploma A minimum of 4 years of related experience or combination of education and relevant experience Proficient in the use of automated and manual measuring devices and test equipment Excellent verbal and written skills in the English language required Skills Preferred experience with layout inspections and sound Geometric Dimensioning and Tolerancing knowledge Preferred experience automating inspection test method is preferred Knowledge of centralizing data for analysis Experience of test and measurement of electronic and/or optical systems Continuous improvement mindset - improves products and processes Well organized and knowledgeable of 6S methodology Demonstrated problem-solving abilities combined with hands-on experience Knowledge of electronic component manufacturing Self-motivated to thoroughly document data and test results Working Conditions Manufacturing working environment. Some areas under cleanroom protocol. Minimal to no expected travel Support of seconds shift operations required This is an on-site position in our Bloomfield, CT facility. Shift will be Monday to Friday 11am to 7:30pm Physical Requirements Must be able to move around manufacturing floor Must be able to lift a maximum of 30 pounds Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ****************************** .

As an essential business, Anomatic produces innovative and sustainable packaging for today's biggest brands. By leveraging over five decades of manufacturing expertise and employing an extensive technologies portfolio, we design, manufacture, and finish incomparable stock and customized solutions for numerous markets. Position: Director of Operations Location: Waterbury, CT Department: Quality Shift: First Shift 6am - 2:30pm JOB SUMMARY QC Stamping Inspector's primary function is the quality evaluation through gauging and inspection to validate the acceptability of stamping production, the capture of nonconforming product and the documenting of that acceptability. Evaluation is conducted as specified through provided gauging and inspection standards. QC Stamping inspectors also provide general “Quality” training, support and guidance to Stamping Department Personnel ESSENTIAL FUNCTIONS Gather samples from each stamping press twice per shift, performs visual and dimensional inspection, recording dimensional results in Mongoose (stamping inspection system of record) as well as on the Stamping Inspection Shift Report (excel file) Conduct proper defect containment, inform the Press Operators of any defects identified, as well as Set-Up personnel, Toolmakers, Tooling Engineer and/or Stamping Dept. Manager as applicable. Record actions (i.e. scrap, hold, etc..) on the Stamping Inspection Shift Report Receive QC LAB (also receiving inspection group) anodizing report, as well as supporting defect samples and address quality issues specified in their report Conduct “outgoing” (from stamping) skid audits for product from presses identified by the Stamping Q.E. Report data as specified Provided training to Stamping Department personnel as a qualified TWI trainer (Includes but not limited to developing TWI instructional break downs, providing individual training for TWI, documenting & tracking provided training, auditing TWI tasks as indicated by management) For Start-up ensure that proper documentation and standards are at each press (gauge plan, part drawing, skid tags, skid labels, and standard boards) Perform “Start-Up” inspection using applicable gauge plan, applicable standard boards and past start-up retains. Record all results on Stamping Inspection Report Maintain “Start-Up Retains Bank” located in the Toolmaker work area. As startups are approved, one raw and one anodized sample from the Start-up will be marked with the approval date and placed in the appropriate bin to be referenced on future start ups At the beginning of each shift Stamping Q.C. Inspectors will review each press and ensure correct labels, gauge plan, part drawing and correct skid tags are being used Keep Department QC Stations and/or QC Work Areas orderly at all times. Double check to make sure proper prints, gauging and inspection plans are at each press and in the QC areas as assigned. Inspect and report inspection results for New Product Development (NPD) by completing the applicable Stamping Quality portion of the First Piece Submission Routing Form Any other duties that may be assigned, including data entry, QC checks on discrepant materials, production and quality reporting, filing and maintaining paperwork, etc. Assist with any other duties and projects as required QUALIFICATIONS Must be proficient in gauging methods and procedures. Must maintain an excellent attendance record. Must be able to work independently without constant supervision and be able to work overtime as needed to cover absences. Must be proficient in the use of Microsoft Office Applications (Outlook, Excel, Word and Power Point at a minimum). Must have basic knowledge of or be trainable on Syteline. Must be able to wear prescribed safety equipment and promote a safe work environment. #1Anomatic

A manufacturing company in Norwalk, CT is looking for a Quality Control Operator. The ideal candidate will have a keen eye for detail, strong analytical skills, and a commitment to continuous improvement. Primary responsibilities will involve monitoring the production process, conducting routine inspections, and performing tests on materials and finished products. You will work closely with production teams to identify and rectify any quality issues, ensuring compliance with industry regulations and internal standards. The Quality Control Operator will also be responsible for maintaining accurate records of inspections and tests, providing feedback to team members, and assisting in the development of quality control procedures. Responsibilities Conduct routine inspections of products during various manufacturing stages. Perform tests on raw materials and finished products to ensure compliance with quality standards. Document inspection results and communicate findings to relevant team members. Identify and report any quality issues or deviations from established standards. Collaborate with production teams to implement corrective actions and improve processes. Assist in the development and maintenance of quality control procedures and protocols. Participate in internal audits and assist with external audits as needed. Requirements High school diploma or equivalent; additional certifications in quality control preferred. Proven experience in a quality control role, preferably in a manufacturing environment. Strong attention to detail and excellent analytical skills. Ability to interpret technical documents, blueprints, and quality standards. Strong communication skills, both written and verbal, with the ability to work effectively in a team. Pay is $22/hr Hours are Monday - Friday 7:50am - 4:20pm. Must be able to pass background check.

Job Description At Sheffield Pharmaceuticals, the home of the original Sheffield Toothpaste, we offer exclusive, quality, branded products to promote wellness and relief to our customers. Our wellness and first aid products include a variety of creams and ointments, nasal products, and toothpaste all made in the USA since 1850. We are currently seeking a junior level quality focused QC Chemist with analytical or quality control laboratory experience in a Manufacturing environment. EDUCATION/EXPERIENCE: Bachelors degree in chemistry or related field. Minimum of one-year experience in analytical or quality control laboratory preferred. DUTIES: Under direction from the Laboratory Supervisor, performs quality control analysis on raw materials, in-process samples, finished/filled products, process validation/evaluation, and stability testing Routine, repetitive checking and testing of production product, including visual and sample inspections of parts used, weights, and measures Inspects production equipment for various Q.C. aspects Maintains proper documentation for Filling department quality control Assists in experiments relative to the discovery and development of new products Makes pilot batches of experimental products Creates processing batch sheets and batch records (PBR's), and checks artwork, crimp codes, log sheets, & shipping requirements Prepare artwork ingredient list General electronic and hard copy file, records, documents and database maintenance Maintain cleanliness and appearance of department, and assist in the disposal of hazardous (laboratory) waste Assist in laboratory instrument qualification and/or calibration Act as subject matter expert for laboratory instrumentation or analytical techniques Maintain proper liaison with all departments to contribute to the team philosophy Responsible for following all safety regulations and complying with S.O.P.'s, DEP, EPA, OSHA, FDA, and cGMP's while performing duties Sheffield Pharmaceuticals is an Equal Employment Opportunity employer. We provide equal opportunity to employees and applicants for employment without regard to race, creed, color, religion, sex, age, national origin, physical or mental disability, sexual orientation, marital or familial status, genetic information, protected veteran status, or other basis protected by law.'

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Working with some supervision, applies established knowledge of laboratory techniques such as HPLC, dissolution, UV/VIS spectrophotometry, moisture by KF, and others to perform product stability testing. • Candidate will be responsible for understanding and performing routine analytical testing for stability samples, evaluating and documenting results in a timely manner. Understands and follows all SOPs and written test procedures. • Performs testing within established standard test times and maintains quality and productivity at acceptable levels as communicated by the supervisor. Candidate will execute troubleshooting of instrumentation and will be expected to maintain laboratory equipment in good working condition. • Candidate will perform laboratory investigation steps with appropriate approvals and with some guidance from supervisor. Keeps supervisor fully informed of all results and project status on a daily basis and reports critical information in a timely manner. Qualifications • Qualifications: Essential Skills- 1-3 years of experience in a related laboratory, HPLC, Dissolution, UV/VIS spectrometry, moisture by KF. Strong understanding of GMP concepts and requirements is desired. • Empower (CDAS) experience is desirable Additional Information For more information, please contact, Sneha Shrivastava **********

Nature and Scope This position is centered on testing of raw materials, in-process, and finished product samples accurately and efficiently to determine chemical identity, potency and purity of pharmaceutical products manufactured by American Regent, Inc. The QC Chemist I will perform analytical testing according to current guidance and established procedures for analysis of stability samples in the Quality Control Laboratories. Essential Duties and Responsibilities Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. * Successfully operate all instruments including: pH meter Balances Autotitrator / Karl Fischer Titrator HPLC / GC ICP-OES / ICP-MS UV-VIS Spectrophotometer Osmometer Polarograph * Perform testing of raw materials, in-process, and finished product samples. * Perform all wet chemistry procedures including titrations, extractions, etc. * General glassware and laboratory cleaning. * Maintain GMP documentation of all activities. * Perform calibration, basic troubleshooting and maintenance on laboratory instruments. * Perform any other tasks/duties as assigned by management. Education Requirements and Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. * Bachelor's degree in Science, Chemistry, Biology or related field required. * Good oral and written communication skills, detail oriented, capable of multi-tasking. * Knowledge of HPLC instrumentation and software. * Knowledge of MS Word, Excel. * Ability to work overtime as needed. Physical Environment and Requirements * Specific vision requirements include 20/40 near vision (can be corrected with eyeglasses or contacts) and color vision. Expected Hourly Rate: $33.70 - $37.00 The hourly rate displayed is the hourly rate of compensation for the role that the employer in good faith believes to be accurate at the time of the posting of an advertisement for the role. Actual compensation for the role will be based on a number of different factors including but not limited to the candidate's qualifications, education, knowledge, skills and experience. American Regent also offers a competitive total rewards package which includes healthcare, life insurance, profit sharing, paid time off, matching 401k as well as a wide range of other benefits. American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status. Applicants have rights under Federal Employment Laws. * FMLA poster: ********************************************************** * Know Your Rights: Know Your Rights: Workplace discrimination is illegal (eeoc.gov) * Employee Polygraph Protection Act: ********************************************************* Alert: We're aware of individuals impersonating our staff to target job seekers. Please note: * All legitimate communication will come directly from a verified ARI recruiter either by phone or via an americanregent.com email address. * Our recruiting process includes multiple in person and/or video interviews and assessments. * If you are unsure about the legitimacy of a message, contact John Rossini at *************************** before responding. * We never request payment, bank information, or personal financial details during our offer process. Your security is important to us, and we encourage you to stay vigilant when job searching. American Regent Inc. endeavors to make *********************************** accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email **************************************.

Job Purpose for Inspector: Maintains quality standards by approving incoming materials, in-process production, and finished products and recording quality results. Duties of Bench Inspector: * Approves in-process and finished products by confirming specifications; conducting visual and measurement tests. * Working from purchase orders, special process certifications, operation sheets, blueprints, and other specifications, ensures that all parts and materials are in full compliance. * Performs complex dimensional layout inspection to operation sheet/blueprint. * Completes Inspection Method Sheets and verifies special process certifications to part specifications. * Performs 1st piece/FAI. Has proven knowledge of Inspection Xpert/Net-Inspect a plus. Aerospace Bench Inspector Skills/Qualifications: * Layout experience is a plus * 0-8 years experience as an inspector in Aerospace or similar industry * Analyzing manufacturing methods and procedures * GD&T skills are highly emphasized * Solid verbal and interpersonal skills, analytical and shop math skills, as well as working knowledge of Microsoft Excel It is the policy of this company to extend equal employment opportunities to all qualified employees without regard to race, color, religion, creed, marital status, learning disability, sexual orientation, national origin, sex, age, history of mental illness, mental retardation or physical, unless such disability prevents performance of the work involved. This policy applies to all phases of employment including, but not limited to, recruitment, hiring, placement, upgrading and promotion, transfer, layoff and recall, termination, selection for company sponsored training programs, rates of pay and other forms of compensation, use of facilities, and participation in all company sponsored activities.

Quality Inspector - Precision Parts | Direct Hire $17-$30 per hour, based on experience Love working with precision? Here's your chance to put your skills to the test! We're hiring a Quality Inspector to ensure every part meets exact standards. If you thrive on accuracy, this role is for you. What You'll Do: Inspect incoming, in-process, and finished metal parts Work with tight tolerances and detailed specifications Read and interpret blueprints / GD&T Play a key role in delivering top-quality products What You Bring: Hands-on inspection experience with close tolerances Strong GD&T and blueprint reading skills Stable work history in quality/manufacturing Aerospace background = big plus! Why You'll Love It: Direct hire opportunity Competitive pay: $17-$30/hr DOE Join a team that values precision and craftsmanship Your attention to detail could be exactly what we're looking for. Apply today and take your quality control career to the next level! A.R. Mazzotta is an equal opportunity employer. It is the policy of A.R. Mazzotta to employ, recruit, hire, train and promote individuals without regard to race, color, religious creed, sex, national origin, age, marital status, present or past history of mental disability, intellectual disability, learning disability, or physical disability, religion, political affiliation or belief, pregnancy, ancestry, veteran status, sexual orientation, gender identity or expression or any other status protected by federal, state, or local laws.

Job DescriptionQuality Inspector - Precision Parts | Direct Hire $17-$30 per hour, based on experience Love working with precision? Here's your chance to put your skills to the test! We're hiring a Quality Inspector to ensure every part meets exact standards. If you thrive on accuracy, this role is for you. What You'll Do: Inspect incoming, in-process, and finished metal parts Work with tight tolerances and detailed specifications Read and interpret blueprints / GD&T Play a key role in delivering top-quality products What You Bring: Hands-on inspection experience with close tolerances Strong GD&T and blueprint reading skills Stable work history in quality/manufacturing Aerospace background = big plus! Why You'll Love It: Direct hire opportunity Competitive pay: $17-$30/hr DOE Join a team that values precision and craftsmanship Your attention to detail could be exactly what we're looking for. Apply today and take your quality control career to the next level! A.R. Mazzotta is an equal opportunity employer. It is the policy of A.R. Mazzotta to employ, recruit, hire, train and promote individuals without regard to race, color, religious creed, sex, national origin, age, marital status, present or past history of mental disability, intellectual disability, learning disability, or physical disability, religion, political affiliation or belief, pregnancy, ancestry, veteran status, sexual orientation, gender identity or expression or any other status protected by federal, state, or local laws.

Pay Range: $30-45 Must be a US Citizen or US Person (Greencard Holder) to apply. This is a W2 contract with a 4-month duration. Seeking a Quality Control Inspector for our client specializing in aerospace and defense products. Must have the ability to work autonomously as well as collaborate effectively with a team and be capable of maintaining precision in a fast-paced environment while meeting deadlines. Responsibilities: * Inspect material (incoming and in-process per J-STD, IPC, and NASA standards) * Minimal lifting (under 25 pounds) * Provide Quality control activities * Document non-conformances and report major quality issues to leadership * First Article inspection Qualifications to Apply: * Certified inspector in MIL/Aerospace workmanship: J-STD, IPC-6110, NASA * US Person or Citizenship * HS Diploma or GED required, advanced degrees desired. * Minimum 5 years of experience gained in a manufacturing environment. * Technically competent, able to read and interpret engineering drawings. Benefits provided: 401K, medical, dental, and vision, sick time as applicable to state law Butler America Aerospace, LLC. is an equal opportunity employer. Butler evaluates applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information and other legally protected characteristics. The Butler America Aerospace, LLC. EEO Policy Statement and "Know Your Rights" Poster is available here: Applicant and Employee Notices. #zr Butler America Aerospace, LLC. is committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process, please contact the Human Resources Department at accommodations@butler.com. #ZR

The Scientist 3 - QC is responsible to perform testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculate and report results on applicable specification documents, participate in method transfer activities within departments or between facilities or organizations. This role will also provide feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. Essential Functions: Perform physical and chemical analysis of raw materials, in-process, and finished pharmaceutical products, including products on stability, according to written methods, material specification, and company policies as identified in standard operating procedures (SOPs). Comply with cGMps, SOPs, and STPs to avoid out-of-specification situation. Assure compliance with state and federal regulations. Actively participate in any project work as and when assigned. Perform process validation and cleaning validation/verification testing on various drugs. Assist other scientists with analytical, instrument and software related problems as required. Use sonic sifter, laser diffraction, Karl Fischer, UV-Vis spectrophotometer, Infra-red spectrophotometer, HPLC with UV detection as well as with conductivity detection, TLC, pH meter, and dissolution. Calibrate HPLC, Dissolution apparatus equipped with auto-sampler and /or in-line UV, pH meters, analytical balances, and Karl-Fischer titrator. Document steps followed during analysis execution, calculate and report results. Actively participate in investigation of laboratory results. Review laboratory analysis data for completeness, specification compliance, and compliance with company's written policies. Report any abnormal findings to the Supervisor. As assigned, perform in-depth review of analytical records/reports to assure that calculations and other data are technically correct and compliant to relevant specifications. Additional Responsibilities: Assist the laboratory supervisor with handling non-routine special projects requiring activities such as out-of-specification investigations and out-of-alert limit investigations in the laboratory. Ensure that expired chemicals and reference standards are removed from laboratory area. Perform calibration of HPLC, GC, and other equipment as assigned by the supervisor. Assist with hands-on training of newly hired Technicians or Scientists 1 and 2 levels. Education: Bachelors Degree (BA/BS) Chemistry or related science discipline - Required Master Degree (MS/MA) Chemistry or related science discipline - Preferred Experience: With a Bachelors Degree (BA/BS) -5 years or more of testing of chemicals/pharmaceutical products With a Masters Degree (BA/BS) -3 years or more of testing of chemicals/pharmaceutical products Skills: Must be precise and consistent in day to day analysis, easily trainable and ready to learn. - Advanced Must be able to work in a team environment and be flexible to easily adapt to changes in assignments. - Advanced Must be able to execute compendial procedures involving complexity with no or minimal supervision. - Intermediate Must be able to effectively communicate results, problems or issues, verbally as well as in writing. - Intermediate Must be able to assume a role of a leader in team environment as and when required. - Intermediate Must be computer literate and savvy with MS office applications, software programs related to LIMS. - Intermediate Must be willing to work extended hours, including weekends, as and when required. - Intermediate Must follow safe practices as identified in appropriate MSDS during working with chemicals, and must follow applicable state and federal regulations. - Advanced Must be capable of maintaining clear and concise laboratory records and communicating clearly both within and between departments. - Advanced Must be thoroughly familiar with cGMP applicable to laboratories in pharmaceutical settings and with method verification/validation concepts. - Advanced Must be able to review laboratory records to ascertain compliance with applicable specifications, methods, and SOPs. - Intermediate Specialized Knowledge: Must possess in-depth knowledge of analytical chemistry techniques, such as spectrophotometric, dissolution and drug release, chromatographic techniques (standalone or hypenated) and measuring physical parameters (viscosity, particle size or droplet size by laser diffraction, melting point by DSC, water content by TGA, identification by XRPD, and other techniques). Must be able to follow compendial (USP/EP/BP/JP) procedures for analysis. Must understand and apply cGMP requirements applicable to quality control laboratory. Must have ability to apply advanced technical skills to troubleshoot and resolve complex analytical and instrument-related problems effectively and in a timely manner and report actions to the laboratory management in a timely manner. Must be able to identify trends in analytical data. The base salary for this position ranges from $90,000 to $95,000 per year. Amneal ranges reflect the Company's good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that helps you enjoy your career alongside life's many other commitments and opportunities.

Job DescriptionBenefits: 401(k) matching Dental insurance Health insurance Paid time off Structural Steel Certified Welding Inspector (CWI)/QC) Structural steel fabricator in Calverton NY is seeking an experienced Certified Welding Inspector (CWI). We are looking for a team player with experience in AISC standards and audits. This is a non-traveling position, which reports to the QC Manager. EDUCATION EXPERIENCE: High school diploma or equivalency certificate. 3+ years of experience as a certified welding inspector in a structural steel fabrication facility, as well as experience in Quality Assurance. Current American Welding Society certified welding inspector (CWI). Ability to read and understand drawings plans and specifications. Ability to perform physical activities that require frequent bending at the waist, squatting, climbing, kneeling and reaching about the head. Must be detail-oriented, extremely organized and have a good work ethic. Microsoft Office skills, including Excel, required. Experience working in fabrication shop UT and MT certification is required AISC standards/audit experience highly preferred. RESPONSIBILITIES: Maintain Quality Control Manual, including compliance to all AISC standards. Position involves visual inspection of structural steel, including bolted and welded connections, and performing non-destructive testing. Interpret codes and specifications in accordance with the drawing requirements. Use a computer to compile and submit data of acceptance or rejection of inspections, as well as for inter-office communications and audit program management. Recommend and approve repairs as well as perform visual inspection of work in progress and completed work. Review and verify welding procedures and welder qualifications. Review Mill test reports and certifications

Job Title: Inspector Quality Control- 1st Article Inspector Department: MPA Warehouse Reports To: Quality Control Manager FLSA Status: Hourly Non-Exempt In- Direct Position Date: 11/17/25 Work Hours: 7:00AM - 3:30PM SUMMARY Responsible for performing detailed inspections on New GG8 spare parts and Customer owner tooling using overhaul manuals, standard practice manuals and WGPW established procedures. Strong-dimensional skills, drawing interpretation are required and previous experience in the aerospace industry is a strong plus. ESSENTIAL DUTIES AND RESPONSIBILITIES The position includes but is not limited to the following essential duties and responsibilities. Maintains a safe and clean work area and adheres to all housekeeping requirements. Follows all safety procedures and rules and properly wears all safety protective equipment as required. Able to read and understand Pratt & Whitney engine manuals, blue prints, service bulletins, illustrated parts catalogs, standard practice, and spare parts bulletins. Able to understand GD&T and drawing interpretation. Able to process quality transactions in ERP system, including non-conformities. Able to use basic shop measuring equipment including Micrometers, Vernier and Dial Calipers, Plunge and Test Indicators, Dial Bore Gages, Snap Gages, profilometer, and PI-Tapes. Working knowledge of a Window's based computer system. Works overtime as required. Conducts oneself in a business-like manner and in the spirit of teamwork. Receiving Inspection: Visual and dimensional inspection of various gas generators using MPA overhaul manuals and WGPW technical data. May be required to work at other WGPW locations or departments due to fluctuating workloads. Able to approve AS9102 First Article Inspection, including certification package and Supplier/Vendor inspection reports. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Experience with job audits, including internal ISO9001 audits. Ability to calculate figures such as ratios, area, circumference, and volume. Ability to apply the basic concepts of algebra, geometry, trigonometry, and shop math as they relate to inspection or trouble shooting. EDUCATION and/or EXPERIENCE Equivalent to high school plus additional broad specialized training in the Quality Control field or technical school, military training and one to three years related experience; or equivalent combination of education and experience. PHYSICAL & ENVIRONMENTAL DEMANDS While performing the duties of this job, the employee is regularly required to sit, stand, and use hands to handle parts. The employee must occasionally lift and move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. While performing the duties of this job, the employee may occasionally work with chemicals while receiving consumable materials in for use on parts within the shop. Possible use of alcohol and/or acetone for light cleanings of oils or dirt as parts are prepared for inspection. WGPW Industrial Turbine Services is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, disability, genetic information, pregnancy, citizenship, marital status, sex/gender, sexual preference/ orientation, gender identity, age, veteran status, national origin, or any other status protected by law or regulation.

Job Description Enjet Aero machines and fabricates complex jet engine parts, components and assemblies for leading OEMs in the commercial, defense and general aviation sectors. Our goal is to be regarded as an irreplaceable resource by our customers. The only way for a company to meet such a goal is to consistently meet production deadlines and expectations. Position Description: Quality Inspector will perform in-process and 1st article inspections, evaluate part to print specifications and understand the inspection methods used for inspection and support the manufacturing process and personnel, while adhering to the Quality Policy, AS 9100 requirements. Position reports to the Quality Manager and takes daily direction from the Inspection Supervisor. You will receive a 20% night shift premium. Essential Responsibilities: Strong blueprint and Geometric Dimensioning & Tolerance (GD&T) comprehension Able to use inspection tools, such as micrometer, indicators, comparator, etc Detailed to complete all paperwork, as required, including inspection reports Able to make mold casts to check ID dimensions Ability to identify dimensional and visual defects Able to understand and implement customer specifications and requirements Accuracy and attention to detail is highly important Experienced with completing 1st article inspections, in-process inspections and final inspections Knowledge of aerospace specifications and requirements preferred. Perform other duties as required Qualifications: Proficient at reading blueprints Knowledge of dimensional symbols Ability to identify visual defects Ability to read micrometers, calipers and comparator Knowledge of measuring equipment Ability to work together for team effort Team oriented Organized and detail oriented Adherence to document control requirements Knowledge of various inspection reports General computer knowledge Ability to work without supervision Benefits: Enjet offers a comprehensive benefits package to full-time employees including paid time off, health insurance, dental insurance, vision insurance, paid holidays, a 401K retirement plan, disability insurance, and more. As an EOE/AA employer, Enjet Aero will not discriminate in its employment practices due to an applicant's race, color, religious creed, national origin, ancestry, sex, age, veteran status, marital status or physical challenges.

Our QC Inspector supports Mativ's Sustainable & Adhesive Solutions Function. This individual will perform inspections and tests throughout the manufacturing process to ensure compliance with specifications under the supervision of Quality Engineering. The shift schedule is 6pm-6am. responsibilities: * Performs all auditing and testing of in-process, and finished goods to include Retain, Coat Weight, Cure and any additional testing as required by the Product Requirement Sheet, (PRS) or Tech 11. * Record and enter test results into the Scapa ERP System * Perform all manufacturing audits prior to production and at required intervals. * Maintain and organize product master files. * Coordinate shop floor QC testing based on daily and weekly production schedule. * Issue non-conformance report for any tested material that is out of specification. * Perform visual inspections of materials being coated and slit/converted and immediately inform coating/converting operators of any defects. * Interfaces with Quality Assurance and Production scheduling in the preparation and reviewing of slitting specifications. * Evaluates product quality based on product specifications and makes appropriate usage decisions. * Responsible for setting up test equipment. * Maintaining inventory of QC lab MRO items * Responsible for maintaining all related files and documents according to Good Documentation Practice, (GDP). * Assists in training new QA Inspectors and manufacturing personnel. * Participates as a team member in continuous improvement events. * Maintain QC test equipment and calibration status. * Assists quality engineers and quality technicians with gage R&R, and other validation activities. * Follows safety rules and keeps the work area in a clean and orderly manner. * Complies with company attendance policies. * Issue Supplier Complaints in the ICS, (Internal Complaint System), for nonconforming raw material. qualifications: Required * Minimum of 2 years' experience in Q. A. or Q. C. manufacturing environment. * High School diploma required, bachelor's degree highly preferred. * Familiar with basic measurements, test equipment and basic math skills. * Medical device industry experience preferred. * Ability to communicate and work within a team environment. * Fluency in English both verbal and written Preferred * 2 years' experience in Quality Assurance or Quality Control. * 2 years' experience in medical device or industrial manufacturing. * Associate degree in chemistry, physical sciences, or tech field. Relevant job experience may be considered in place of a 2-year degree. * Able to collaborate and work well with others. Position Demands Conditions are that of a manufacturing environment: * Air Temperatures can range from cold to hot. * The atmosphere may contain dust, fumes, and odors. * May include mechanical, electrical, chemical, explosive and radiation hazards. Employees are required to wear Personal Protective Equipment (PPE) including: * Safety shoes (steel toe or composite toe) * Safety Glasses * Bump Caps * Protective Gloves, when performing certain tasks * Hearing Protection, when required. * Other personal protective equipment as required for certain tasks. While performing the duties of this job the employee must meet the physical demands: * Be able to lift a minimum of 50 pounds. * Be able to work 12-hour shifts. * Perform repetitive tasks. * Routinely stand, sit, hear, walk, and talk. * Reach, climb, bend, kneel, crouch, twist, and balance, sometimes in awkward or tight spaces. * Have good close vision, depth perception, and the ability to focus. WHAT WE OFFER At Mativ, our benefits reflect how much we value and care for each other. We know that employees and their families have unique needs, so our comprehensive benefits offer flexibility, quality, and affordability. Here are just a few of the ways we support your well-being and that of your loved ones: * Medical, dental and vision insurance * Consumer-Driven Health Plan (CDHP) * Preferred Provider Organization (PPO) * Exclusive Provider Organization (EPO) * Company-paid basic life insurance and Additional voluntary life coverage * Paid vacation and competitive personal time off * 401(k) savings plan with company match * Employee assistance programs - available 24/7 to you and your family * Wellness and Work Life Support - career development and educational assistance ABOUT MATIV Mativ Holdings, Inc. is a global leader in specialty materials headquartered in Alpharetta, Georgia. The company connects, protects, and purifies the world every day through a wide range of critical components and engineered solutions that solve our customers' most complex challenges. We manufacture on three continents and generate sales in nearly 100 countries through our family of business-to-business and consumer product brands. The company's two segments, Filtration & Advanced Materials and Sustainable & Adhesive Solutions, target premium applications across diversified and growing end-markets, from filtration to healthcare to sustainable packaging and more. Our broad portfolio of technologies combines polymers, fibers, and resins to optimize the performance of our customers' products across multiple stages of the value chain. Our leading positions are a testament to our best-in-class global manufacturing, supply chain, and materials science capabilities. We drive innovation and enhance performance, finding potential in the impossible. Mativ and its subsidiaries are Equal Opportunity Employers. Qualified applicants will be considered without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.